epoxide in organic synthesiskanai/seminar/pdf/lit_y_hirao_m1_2.pdf · organic synthesis m1 yuki...
TRANSCRIPT
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Epoxidein
Organic Synthesis
M1 Yuki Hirao
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2
Introduction
Epoxides are important intermediates in total synthesis.
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3
Asymmetric Epoxidation
The Nobel Prize
in Chemistry 2001
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4
Contents
1. Introduction
2. Ring-Opening of Epoxide・Nucleophilic addition
・Reductive-opening by SET
3. Titanocene-catalyzed Epoxide Opening
4. Recent Achievements・Isomerization of epoxides to Allylic Alcohols
・Anti-Markovnikov alcohols via epoxide
hydrogenation
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5
Ring-Opening of Epoxide
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Nucleophilic addition
Jacobsen, E, N. et al. J. Org. Chem. 1997, 62, 4197.
Jacobsen, E, N. et al. Tetrahedron Lett. 1997, 38, 773.
Jacobsen, E, N. et al. Science. 1997, 277, 936.
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7
Reductive-opening by SET
Opening of epoxides with low-valent metal complexes
General Ideas
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8
Reductive-opening by SET
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9
Reductive-opening by SET
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10
Contents
1. Introduction
2. Ring-Opening of Epoxide・Nucleophilic addition
・Reductive-opening by SET
3. Titanocene-catalyzed Epoxide Opening
4. Recent Achievements・Isomerization of epoxides to Allylic Alcohols
・Anti-Markovnikov alcohols via epoxide
hydrogenation
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Titanocene-catalyzed Epoxide Opening
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Titanocene-catalyzed Epoxide Opening
Fürstner, A. et al. J. Am. Chem. Soc. 1995, 117, 4468.
Fürstner, A. et al. J. Am. Chem. Soc. 1996, 118, 2533.
Ikeda, I. et al. J. Org. Chem. 1996, 61, 366.
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Titanocene-catalyzed Epoxide Opening
A. Gansäuer. et al. J. Org. Chem. 1998, 66, 2070.
A. Gansäuer. et al. Eur. J. Org. Chem. 1998, 2673.
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14
Titanocene-catalyzed Epoxide Opening
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Computational Studies
A. Gansäuer. et al. J. Am. Chem. Soc. 2007, 129, 1359.
DFT calculations (BP86/TZVP)
Favored Disfavored
In disfavored transition state, the larger CH3 group gets into closer contact with Cp ligand.
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Computational Studies
A. Gansäuer. et al. J. Am. Chem. Soc. 2007, 129, 1359.
DFT calculations (BP86/TZVP)
Epoxide opening is exothermic. The formation of the higher substituted radicals is thermodynamically
favored.
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17A. Gansäuer. et al. J. Am. Chem. Soc. 1998, 120, 12849.
A. Gansäuer. et al. J. Am. Chem. Soc. 2007, 129, 1359.
Computational Studies
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Titanocene-catalyzed Epoxide Opening
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Short Summary
Reductive Opening of Epoxides by SETRadical Stability
Steric Interactions between R1, R2 and Cp ligand
more highly substituted radical
opposed to SN2 Reaction (from less substituted carbon)
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Contents
4. Recent Achievements
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Purpose
J. Andersson. et al. J. Am. Chem. Soc. 2000, 122, 6610.
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Optimization
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Proposed Catalytic Cycle
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Substrate Scope
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Kinetic Resolution
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Radical Rearrangement
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Asymmetric Reaction
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Contents
4. Recent Achievements
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Anti-Markovnikov alcohols
C. Yao, T, Dahmen, A. Gansäuer, J. Norton. Science. 2019, 364, 764.
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Previous Work
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This Work
C. Yao, T, Dahmen, A. Gansäuer, J. Norton. Science. 2019, 364, 764.
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Proposed Catalytic Cycle
C. Yao, T, Dahmen, A. Gansäuer, J. Norton. Science. 2019, 364, 764.
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Side Reaction
C. Yao, T, Dahmen, A. Gansäuer, J. Norton. Science. 2019, 364, 764.
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Substrate Scope
C. Yao, T, Dahmen, A. Gansäuer, J. Norton. Science. 2019, 364, 764.
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Substrate Scope
C. Yao, T, Dahmen, A. Gansäuer, J. Norton. Science. 2019, 364, 764.
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Summary
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Appendix
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Titanocene-catalyzed Epoxide Opening
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Unsuccessful Substrates Isomerization of epoxides to Allylic Alcohols
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Radical Rearrangement
K. Y. Ye, T. M. Callum, S. Lin. J. Am. Chem. Soc. 2019, 141, 9548.
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Cyclic Voltammetry Studies
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Optimization of anti-Markovnikov hydrogenation
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NMR Studies
C. Yao, T, Dahmen, A. Gansäuer, J. Norton. Science. 2019, 364, 764.
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NMR Studies
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NMR Studies
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Cyclic Voltammetry Studies