ncc+ gm 62606 · 2006-06-26 · outline 1. introduction 2. the nonclassical carbocation controversy...
TRANSCRIPT
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Nonclassical CarbocationsFrom Controversy to Convention
A Stoltz Group Literature Meetingbrought to you by
Chris Gilmore
June 26, 20068 PM
147 Noyes
C
H
H H
H
H
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Outline
1. Introduction
2. The Nonclassical Carbocation Controversy - Winstein, Brown, and the Great Debate - George Olah and ending the discussion - Important nonclassical carbocations
3. The Nature of the Nonclassical Carbocation - The 3-center, 2-electron bond - Cleaving C-C and C-H σ−bonds - Intermediate or Transition state? Changing the way we think about carbocations 4. Carbocations, nonclassical intermediates, and synthetic chemistry - Biosynthetic Pathways - Steroids, by W.S. Johnson - Corey's foray into carbocationic cascades - Interesting rearrangements - Overman and the Prins-Pinacol
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R
R
RLGR
RR
superacid
LGH "carbeniumion"
- 6 valence e-
- planar structure- empty p orbital
RRR
Carbocations: An Introduction
Traditional carbocation is a low-valent, trisubstituted electron-deficient carbon center:
Modes of stabilization:
X
X RH2C
Heteroatomic Assistance π-bond Resonance σ-bond Participation
Lone PairResonance
AnchimericAssistance
AllylicStabilization Homoconjugation Hyperconjugation Non-Classical
Interaction
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Outline
1. Introduction
2. The Nonclassical Carbocation Controversy - Winstein, Brown, and the Great Debate - George Olah and ending the discussion - Important nonclassical carbocations
3. The Nature of the Nonclassical Carbocation - The 3-center, 2-electron bond - Cleaving C-C and C-H σ−bonds - Intermediate or Transition state? Changing the way we think about carbocations 4. Carbocations, nonclassical intermediates, and synthetic chemistry - Biosynthetic Pathways - Steroids, by W.S. Johnson - Corey's foray into carbocationic cascades - Interesting rearrangements - Overman and the Prins-Pinacol
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The Nonclassical Problem: Early Curiosities
Wagner, 1899:
OHH
- H+
1,2 shift
OH
Ruzicka, 1918:
Meerwein, 1922:
OH
Nuc
Nuc
Nuc
1,2 shift
Ruzicka, L. Helv. Chim. Acta, 1918, 1, 110.
Meerwin, H. Chem. Ber. 1922, 55B, 2500.
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The Nonclassical Problem: An Indecent ProposalWinstein and Trifan, 1949
OBsOBs
Rates of solvolysis
350 1
aqueous solvent aqueous solvent
Winstein, Trifan. J. Am. Chem. Soc., 1949, 71, 2953.
O SO
OBr
= OBs
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The Nonclassical Problem: An Indecent Proposal
OBs2
7
3
16
5 Acetone, H2O
KOAc
Winstein and Trifan, 1949
OAc
OAc
AcO
13
2
7
5
6
1
72
4
4
56
3
2 1
6
OAc1:1 Mixture of enantiomers
OBsOBs
Rates of solvolysis
Enantiomerically pure starting material...
350 1
aqueous solvent aqueous solvent
Winstein, Trifan. J. Am. Chem. Soc., 1949, 71, 2953.
O SO
OBr
= OBs
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The Nonclassical Problem: An Indecent Proposal
OBs2
7
3
16
5Acetone, H2O
KOAc
OAc
OAc
AcO
13
2
7
5
6
1
72
4
4
56
3
2 1
6
OAc 1:1 Mixture of enantiomersWinstein, Trifan. J. Am. Chem. Soc., 1949, 71, 2953.
O SO
OBr
= OBs
Winstein and Trifan, 1949
OBsOBs
Rates of solvolysis
Enantiomerically pure starting material...350 1
aqueous solvent aqueous solvent
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OBs OAc
The Nonclassical Problem: An Indecent Proposal
OAcHOAc
OBsOBs350 1
aqueous solvent aqueous solvent
"It is attractive to account for these results by way of the bridged (nonclassical) formulation for the norbornyl cation involving accelerated rate of formation from the exo precursor by
anchimeric assistance." -Saul Winstein
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OBs OAc
The Nonclassical Problem: An Indecent Proposal
OAcHOAc
OBsOBs350 1
aqueous solvent aqueous solvent
"It is attractive to account for these results by way of the bridged (nonclassical) formulation for the norbornyl cation involving accelerated rate of formation from the exo precursor by
anchimeric assistance." -Saul Winstein
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The Response of the Traditionalists- H. C. Brown
Solvolysis proceeds through unassisted ionization: - relief of strain accelerates endo ionization - steric effects hinder ionization of endo isomer - exo is not fast, endo is slow
OBsOBsOBs
PNBExo/Endo 350 13 78
Not only must strain have some impact, but direct ionization hinders rate of solvolysis of endo norbornyl system.
H
H
LG
H
H
H
H
LG
Brown, H.C. J. Am. Chem. Soc. 1964, 86, 1248-1250.
Strain release improves exo to endo ratio:
exo endo
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A Bonding Experience- Brown's Challenge
"The norbornyl cation does not possess sufficient electrons to provide a pair for all of the bonds required by the
proposed bridged structures. One must propose a new bonding concept, not yet established in carbon structures."
- H. C. Brown, 1965
Brown insisted upon two stable, equilibrating classical carbocaitonic forms for the norbornyl cation:
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A Bonding Experience- Brown's Challenge
"The norbornyl cation does not possess sufficient electrons to provide a pair for all of the bonds required by the
proposed bridged structures. One must propose a new bonding concept, not yet established in carbon structures."
- H. C. Brown, 1965
Brown insisted upon two stable, equilibrating classical carbocaitonic forms for the norbornyl cation:
Brown, H. C. J. Am. Chem. Soc. 1965, 87, 2137-2153.P.D. Bartlett, Nonclassical Ions, W.A. Benjamin, New York, 1965.
So, if not classical carbenium ions, what must nonclassical carbocations be?
R
R R
R
R
- a pentavalent carbon- distinct 3-center, 2-electron bond- 8 valence e- between 6 atoms means electron-poor carbon
"carbonium ion"
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A Bonding Experience- Brown's Challenge
"The norbornyl cation does not possess sufficient electrons to provide a pair for all of the bonds required by the
proposed bridged structures. One must propose a new bonding concept, not yet established in carbon structures."
- H. C. Brown, 1965
Brown insisted upon two stable, equilibrating classical carbocaitonic forms for the norbornyl cation:
So, if not classical carbenium ions, what must nonclassical carbocations be?
R
R R
R
R
- a pentavalent carbon- distinct 3-center, 2-electron bond- 8 valence e- between 6 atoms means electron-poor carbon
BH
BH
H
H
H
H
isoelectronic
Contain too few electrons to allow a pair for each "bond"; must have delocalized σ electrons
P.D. Bartlett, Nonclassical Ions, W.A. Benjamin, New York, 1965.
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Enter George Olah
- Previous work with isolable carbocations possible because of superacids and stable ion media.
- Isolated the first stable carbocation in 1964 and was able to characterize with 13C NMR
- Superacids designed to prevent proton elimination to quench carbocations
- pKa's are measured anhydrously by Hammet acidiy function Ho Hoanhydrous sulfuric acid -11.9perchloric acid -13.0triflic acid -14.1magic acid (FSO3H•SbF5) -21.0
FMe
MeMe
SbF5Me
MeMe SbF6
13C shift was 300 ppm downfield from SM! (335.2 ppm)
MeMe
H
MeMe
H
Superacids can reach acidities of Ho= -28, or 1016 times acidity ofanhydrous sulfuric acid.
J. Am Chem. Soc. 1964, 86, 1360
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Proving the Existence of the Carbonium Ion
F
SbF5
25 °C
Broad singlet correspondsto fast Wagner-Meerwein and hydride shifts, -3.75 — -3.1 ppm
1H NMR Studies of Olah, Saunders and Schleyer
F
SbF5, SO2
-60 to -120°C
Resolves 3 singlets, 4:1:6at -5.35, -3.15, -2.20 ppm
Shows 2-norbornyl ion stable in solution as equilibrating Wagner-Meerwein shifts OR mesomeric intermediate
3,2 shift
W-M
6,2 shift
2
3
6
7
1
Saunders, M.; Schleyer, P.; Olah, G. A. J. Am. Chem. Soc. 1964, 86, 5680.
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Proving the Existence of the Carbonium Ion
F
SbF5
25 °C
Broad singlet correspondsto fast Wagner-Meerwein and hydride shifts, -3.75 — -3.1 ppm
1H NMR Studies of Olah, Saunders and Schleyer
F
SbF5, SO2
-60 to -120°C
4 (-5.35 ppm)
1 (-3.15 ppm)
6 (-2.20 ppm)
3,2 shift
W-M
6,2 shift
2
3
6
7
1
H
HH
HH
HH
HHH
H
HH H
H
HH
H
H
H HH
Saunders, M.; Schleyer, P.; Olah, G. A. J. Am. Chem. Soc. 1964, 86, 5680.
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Proving the Existence of the Carbonium Ion
A
F
SbF5, SO2
-157 °C
2
7
3
16
5
F
SbF5, SO2
-100 °C
B
1,2,6 4 3,5,7
1,2 6 4 7
3,5
Olah, G. A. J. Am. Chem. Soc. 1982, 104, 7105.
1H spectra at low temps
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Proving the Existence of the Carbonium Ion
F
SbF5, SO2
-158 °C
2
7
3
16
5
F
SbF5, SO2
-80 °C
Olah, G. A. J. Am. Chem. Soc. 1982, 104, 7105.
1,2,6 4 3,5,7
1,2
7,6
3,5
4
A
B
13C spectra at low temps
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Proving the Existence of the Carbonium IonCore Electron Spectroscopy for Chemical Analysis (ESCA)
- Exploits photoelectric effect to measure ion affinity for electrons.- Trivalent classical carbocation shows charge localization on 1 atom increases e- binding energy by ~5eV- Timescale is ~ 1018 Hz, much faster than NMR and Wagner-Meerwein shifts
MeMeMe
H
Me
Δ eV = 3.4
Δ eV
Δ eV
Δ eV = 3.7
Δ eV = 4.2 - 4.3
Olah, G. A.; Mateescu, L. A. J. Am. Chem. Soc. 1970, 92, 7231.Olah, G. A.; Mateescu, L. A. J. Am. Chem. Soc. 1972, 94, 2529.
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Proving the Existence of the Carbonium Ion
MeMeMe
H
Me
Δ eV = 3.4
Δ eV
Δ eV = 1.7
Δ eV = 4.2 - 4.3
Δ eV
Core Electron Spectroscopy for Chemical Analysis (ESCA)- Exploits photoelectric effect to measure ion affinity for electrons.- Trivalent classical carbocation shows charge localization on 1 atom increases e- binding energy by ~5eV- Timescale is ~ 1018 Hz, much faster than NMR and Wagner-Meerwein shifts
Olah, G. A.; Mateescu, L. A. J. Am. Chem. Soc. 1970, 92, 7231.Olah, G. A.; Mateescu, L. A. J. Am. Chem. Soc. 1972, 94, 2529.
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Closing the Debate
Solid-state 13C NMR studies at 5 K
2
7
3
16
5 vs.
Calculations revealthat Wagner-Meerweinshifts would require a barrier of 0.2 kcal/moland occur at 105 Hz toavoid resolution at 5 K,setting migration equalto a vibrational transition
Yannoni, C. S.; Myhre, P. C. J. Am. Chem. Soc. 1982, 104, 7381-7383
Isolated crystals allowed x-ray determination of ion's structure:
Me
Me
Me
Me2.092 Å
1.739 Å1.467 Å
1.442 Å
Laube, T. Angew. Chem. Int. Ed. Engl. 1987, 26, 560
For an excellent review of the nonclassical ioncontroversy:
- Olah, G. A.; Prakash, G. K. S.; Saunders, M. Acc. Chem. Res. 1983, 16, 440-449.- Olah, G. A. Angew. Chem. Int. Ed. Engl. 1995, 34, 1393-1405
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Other Important Nonclassical Carbocations
CH
H H
H
H
methonium
CH
HH
H
H
- Parent for all nonclassical carbocations.- 8 Valence electrons rendered deficient by electron pair sharing between 3 atoms
Geometry:- initially suggested trigonal bipyramidal structure- Ab initio calculations postulated Cs symmetry (as shown)- Low bond-bond proton migration barriers lend to completely delocalized theory of bonding
HCHH
H
H
CH
HH
H
H
trigonalbipyramidal
delocalized
Cs
HH
HH
H+ H
HH H
HC
H
H H
H
HC
H
HH
H
H
Olah, G. A.; Klopman, G. J. Am. Chem. Soc. 1969, 91, 3261
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Other Important Nonclassical Carbocations
CH
H H
H
H
cyclopropylcarbinyl
Cl
48%
47%
5%
EtOH,H2O OH
OH
OH
unsymmetricalstabilization
Studies by Roberts in 1951:
Roberts, J.D.; et. al. J. Am. Che. Soc. 1951, 73, 3542.
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Other Important Nonclassical Carbocations
CH
H H
H
H
cyclopropylcarbinyl
Cl
48%
47%
5%
EtOH,H2O OH
OH
OH
unsymmetricalstabilization
Studies by Roberts in 1951:
Schleyer's Solvolytic Studies and Structural Revision in 1966:
DNB
DNB
DNBMeMe
Me
OH
OH
OH
Me
MeMe
krel = 1
krel = 11
krel = 82
DNBMeMe
OHMeMe
krel = 490
Me Me
R RR R
symmetrical stabilization
Schleyer, P. v. R. J. Am. Chem. Soc. 1966, 88, 2321.
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Other Important Nonclassical Carbocations
CH
H H
H
H
7-norbornenyl
TsO
TsO
k1
k2
HOAc
HOAcAcO
AcO
k2/k1 = 1011
Norbornene Solvolysisoccurs with completeretention of stereo-chemistry!
Solvolytic studies by Winstein (JACS 1956, 78, 592)
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Other Important Nonclassical Carbocations
CH
H H
H
H
7-norbornenyl
TsO
TsO
k1
k2
HOAc
HOAcAcO
AcO
k2/k1 = 1011
Norbornene Solvolysisoccurs with completeretention of stereo-chemistry!
Solvolytic studies by Winstein (JACS 1956, 78, 592)
1H NMR study of norbornadienyl model system proved nonequivalence of protons in norbornenyl cation
2
3
6
52,3 @ 2.54 ppm, 5,6 @ 3.90 ppm
Winstein, S.; Brookhart, M. J. Am. Chem. Soc. 1972, 94, 2347.
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Other Important Nonclassical Carbocations
CH
H H
H
H
phenonium ionAromatic group participation
Walden Inversion:
PhOTs
HOAc PhOAc
PhOAc
1 1
Cram, D. D. J. Am. Chem. Soc. 1949, 71, 3183
Me
MeH
H Me
MeH
H
racemization
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Other Important Nonclassical Carbocations
CH
H H
H
H
cyclopropyl assistance
Properties of Cyclopropane are similar to an olefin:
~ ~
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Other Important Nonclassical Carbocations
CH
H H
H
H
cyclopropyl assistanceProblem solved by solvolysis
BsO
OBs
OBs
OBs
OAc
OAc
OAc
OAc
krel
1
1014
5
0.333
Tsuji, et. al. J. Am. Chem. Soc. 1967, 89, 1953.; Wells, et. al. Tetrahedron, 1966, 22, 2007.
HOAc
HOAc
HOAc
HOAc
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Outline
1. Introduction
2. The Nonclassical Carbocation Controversy - Winstein, Brown, and the Great Debate - George Olah and ending the discussion - Important nonclassical carbocations
3. The Nature of the Nonclassical Carbocation - The 3-center, 2-electron bond - Cleaving C-C and C-H σ−bonds - Intermediate or Transition state? Changing the way we think about carbocations 4. Carbocations, nonclassical intermediates, and synthetic chemistry - Biosynthetic Pathways - Steroids, by W.S. Johnson - Corey's foray into carbocationic cascades - Interesting rearrangements - Overman and the Prins-Pinacol
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The 3-Center, 2-electron Bond
Postulated first by DeWar in 1945 as π-complex
E+
E+
HB
HB
H H
HHH
BH
BH H
HH
R2B H
BR3
Diborane and the stable 3-center 2-electron bond.
- Borane dimers consist of two 3-center 2-electron bonds- Delocalized electron-poor region at center of dimer
Electon-poor carbon analogs: π-bond donors
Cationic π−complexes and MO theory
E+
CR2R2CR2C CR2
E+
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Protonating an Alkane
Me3C CH3
Much less nucleophilic than π-bonds, σ C-C and C-H bonds donate as well:
Me3C CH2
HH+
Me3C CH2
HH
Me3C CH3
HHF-SbF5
CH4
MeMeMe
H2 Me3CHH
Calculated Protonolysis Activation Barriers (Sb2F11
.HF2 @ 298K)
Alkane ΔHo (kcal/mol)CH4 21.0C2H6
∗
∗
*
*
19.3
19.318.7
19.9
18.3
Calculated C-C Cracking Activation Barriers (Sb2F11
.HF2 @ 298K)
Alkane ΔHo (kcal/mol)
C2H6
C3H8
35.0
30.0
28.7
Mota, et. al. J. Phys. Chem. B 2001, 105, 4331.Ramsden Tetrahedron 2004, 60, 3293.
Olah, et al. Angew. Chem. Int. Ed. Eng. 1973, 12, 173.
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Olah's general order of alkane σ−bond reactivity:H
R RR
R3C CR3
H
R RH
H
R HH
H
H HH
> > > >
Protonating an AlkaneMuch less nucleophilic than π-bonds, σ C-C and C-H bonds donate as well:
Linear or bridged transition state in σ protonation?
HR
R R
HR
R R
R
R R
H
H
H
H+ HR
R R
MeMeMe
A
B
D2, H+ D2, H+HR
RR
HR
R R
DR
R RA B
Olah vs. Hogeveen
Olah, 1971
Olah, et al. J. Am. Chem. Soc. 1971, 93, 1251.Hogeveen, et al. Recl. Trav. Chim. Pays-Bas. 1969, 88, 703.
Olah, et al. Angew. Chem. Int. Ed. Eng. 1973, 12, 173.
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Leveling the Field
The 3-center, 2-electron bond changes how all carbocations are precieved
Ethyl cation: hyperconjugation or hypervalence?
H
H HHH
HH H
H
Hvs.
- Carbenium ions are prone to rearrangement
- Rapid scrambling of 5 H's in ethyl cation indicative of some delocalized intermediate
- Hydride shifts in such cations are illustrative of the low energy barriers between cabenium and carbonium ions
- Carbonium intermediate is calculated as favorable for all but most stabilized carbocations
H
H HMeMe
HH Me
Me
Hvs.
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Leveling the Field
The 3-center, 2-electron bond changes how all carbocations are precieved
Ethyl cation: hyperconjugation or hypervalence?
H
H HHH
HH H
H
Hvs.
- Carbenium ions are prone to rearrangement
- Rapid scrambling of 5 H's in ethyl cation indicative of some delocalized intermediate
- Hydride shifts in such cations are illustrative of the low energy barriers between cabenium and carbonium ions
- Carbonium intermediate is calculated as favorable for all but most stabilized carbocations
H
H HMeMe
HH Me
Me
Hvs.
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Leveling the Field
The 3-center, 2-electron bond changes how all carbocations are precieved
Ethyl cation: hyperconjugation or hypervalence?
H
H HHH
HH H
H
Hvs.
- Carbenium ions are prone to rearrangement
- Rapid scrambling of 5 H's in ethyl cation indicative of some delocalized intermediate
- Hydride shifts in such cations are illustrative of the low energy barriers between cabenium and carbonium ions
- Carbonium intermediate is calculated as favorable for all but most stabilized carbocations
H
H HMeMe
HH Me
Me
Hvs.
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Leveling the Field
The 3-center, 2-electron bond changes how all carbocations are precieved
Ethyl cation: hyperconjugation or hypervalence?
H
H HHH
HH H
H
H
Wagner-Meerwein shifts and isomerization
vs.- Carbenium ions are prone to rearrangement
- Rapid scrambling of 5 H's in ethyl cation indicative of some delocalized intermediate
- Hydride shifts in such cations are illustrative of the low energy barriers between cabenium and carbonium ions
- Carbonium intermediate is calculated as favorable for all but most stabilized carbocations
H
H HMeMe
HH Me
Me
Hvs.
H
H
H - 1 13C NMR Shift at -139 °C
- Rearrangements occur ~ 3.1 x 107 Hz
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A Whole New Ballgame...
Delocalized intermediates also participate in assisting leaving group departure
OLA
OLA
O
OHNuc
OH
Nuc
Prins-Pinacol reaction intermediate resembles a momentarily delocalized cation:
Many of the carbocationic rearrangements basic to organic chemistry can be associated withnonclassical carbocationic intermediates.
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Outline
1. Introduction
2. The Nonclassical Carbocation Controversy - Winstein, Brown, and the Great Debate - George Olah and ending the discussion - Important nonclassical carbocations
3. The Nature of the Nonclassical Carbocation - The 3-center, 2-electron bond - Cleaving C-C and C-H σ−bonds - Intermediate or Transition state? Changing the way we think about carbocations 4. Carbocations, nonclassical intermediates, and synthetic chemistry - Biosynthetic Pathways - Steroids, by W.S. Johnson - Corey's foray into carbocationic cascades - Interesting rearrangements - Overman and the Prins-Pinacol
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Carbocationic Cascades- Biosynthesis
OPP
H
H H
H
H
H
H
H
H
H
HH
H
pentalenene
farnesyl diphosphate
Tantillo J. Am. Chem. Soc. 2006, 128, 6172.
1,2 shift
1,2 shift - H+
- isolated from streptomyces- precursor to pentalenolactone antibiotics
H
H
H
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Carbocationic Cascades- Biosynthesis
OPPfarnesyl diphosphate
H
Hhumulene
H
H
HH
H
asteriscadiene
H
H
H
H
H
Δ6- protoilludene
Tantillo J. Am. Chem. Soc. 2006, 128, 6172.
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W.S. Johnson's Approach to Steroid Skeletons
HO
OHOH
HO HOH H
HSnCl4, DCM
30 min, -100 °C
59% yield
Johnson, W. S.; et. al.Journ. Am. Chem. Soc.1973, 95, 7501.
Johnson, W. S.; et. al.Journ. Am. Chem. Soc.1976, 98, 1038.
Johnson, W. S.; et. al.Journ. Am. Chem. Soc.1973, 95, 4417.
TFA, TFE-100 °C
66% yield
O
H H
H
H H
OO
NTFA, nitroethane
-78°C, 15 min
80% yield
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W.S. Johnson's Approach to Steroid Skeletons
HO HOH H
HSnCl4, DCM
30 min, -100 °C
59% yield
Johnson, W. S.; et. al.Journ. Am. Chem. Soc.1973, 95, 7501.
Johnson, W. S.; et. al.Journ. Am. Chem. Soc.1976, 98, 1038.
Johnson, W. S.; et. al.Journ. Am. Chem. Soc.1973, 95, 4417.
TFA, TFE-100 °C
66% yield
O
H H
H
H H
OO
NTFA, nitroethane
-78°C, 15 min
80% yield
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Carbocationic Cascades- Corey and Oleananes
OMeO
O
H
H HBzO BzOH
O
HO
AlMeCl2MeAlCl3
-78 °C
HHOH
R(+) β-amyrin R= CH3(+) erthrodiol R= CH2OH(+) oleanolic acid R= COOH
Corey, E.J J. Am. Chem. Soc. 1993, 115, 8873-8874
PhCOClDMAP
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Some other unique rearrangements
O
H
HO PhPh
H
OH
PhCl2MeAl
H
OH
PhCl2MeAl
Me
Me
Ph
H
O
H
Cl2MeAl
MePh
H
O
H
Cl2MeAl
Me
MePh
H
O
H
Cl2MeAl Me
HH H
MePh
H
O
H
Cl2MeAlMe
H H
MePh
H
O
H
Cl2MeAl Me
H
H
HO Ph
Corey, E. J.; Roberts, B.E. Tetrahedron Lett. 1997, 38, 8921.
MeAlCl2-95 °C
50% yield
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Some other unique rearrangements
O
O
O
OHO OO
O
RO
RO
NR
O
O
O
O OO
O
RO
RO
NR
FH
Lartey, et. al. J. Org. Chem. 1996, 61, 5153.
DAST
N SF3
Et
Et
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Some other unique rearrangements
O
O
O
OHO OO
O
RO
RO
NR
O
O
O
OO OSF
FN
Et
Et
OOSF
FN
Et
EtOOS
F
FN
Et
Et
O
O
O
O OO
O
RO
RO
NR
FH
Lartey, et. al. J. Org. Chem. 1996, 61, 5153.
DAST
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Cationic Cascade to Longifolene
HOO
HOTFA, Et2O0 °C, 3 min
K2CO3 workup
HO
H+
HO
Johnson, W. S., et. al. J. Am. Chem. Soc. 1975, 97, 4777.Tantillo, D. J., et al. J. Org. Chem. 2005, 70, 5139.
H+
76% yieldlongifolene
K2CO3
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Larry Overman and the Prins-Pinacol N
HH
O
MeOH
H
H
(—)-magellanine
H
HO
Overman, L. E. J. Am. Chem. Soc. 1993, 115, 2992.
O O
TIPSO HHO
H
OHH
SnCl4
-78 °C
57% yield
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Larry Overman and the Prins-Pinacol N
HH
O
MeOH
H
H
(—)-magellanine
H
HO
Overman, L. E. J. Am. Chem. Soc. 1993, 115, 2992.
O O
TIPSO
O Me
TIPSO
OMe
TIPSO
OMe
TIPSO
OMe
O
HHO
H
OHH
SnCl4
-78 °C
57% yield
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Larry Overman and the Prins-Pinacol
Overman, L.E. J. Am. Chem. Soc. 2001, 123, 4851
O
O
AcO
OAc
H
H H
OTMS
SPh
SPhMe Me
SPh
O
H
HO
O
H
H
shahamin K
DMTSF
-45 °C to 0 °C80% yield
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Larry Overman and the Prins-Pinacol
Overman, L.E. J. Am. Chem. Soc. 2001, 123, 4851
O
O
AcO
OAc
H
H H
OTMS
SPh
SPhMe Me
Me
Me
OTMS
H SPh
Me
Me
OTMS
H SPh
SPh
O
H
HO
O
H
H
shahamin K
DMTSF
-45 °C to 0 °C80% yield
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Summary and Parting Thoughts
- The nonclassical carbocation controversy opened the realm of physical organic chemistry, established the idea of delocalized, electron-poor bonding in intermediates and transition states for organic reactions, and encouraged an intense debate that has led to the affirmation of many instrumental and experimental techniques used today
- The 3-center, 2-electron bond is prevalent in carbocation chemistry, often as a stable intermediate or transition state, and sometimes as a stable molecule itself
- Carbocation chemistry and its variants have found an effective place in synthesis, but there exists a large gap in controlled carbocationic methodology that has only recently been explored.
Thanks to JT for the Carbocation book and Meyer for helpful advice