roger oconnor soccgmpres 2016

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3 ROUNDTREE DRIVE, MERRIMACK, NH O3O54 603-341-8405 [email protected] ROGER O’CONNOR SYNTHETIC ORGANIC CHEMIST Focused and very precise experienced research chemist with nearly ten years experience designing and completing synthetic methodologies from retrosynthetic analysis to endgame and spectroscopic analysis and structure determination of natural products, analogues and polypeptides. Also experienced with coordinating off-site syntheses and written/electronic reports and research progress communication and very experienced with 1D and 2D NMR, FTIR and ATR, HPLC, recycling HPLC and GCMS/LCMS. FUNCTIONAL SUMMARY Development of synthetic strategies as well as nearly 10 years experience as bench chemist Experienced with 1 H, 13 C, 19 F, 31 P, HH-COSY, CH-COSY, NOESY, HMQC and other experiments and analysis and precise data processing. Purification of various sythetic samples through recrystallization, chromatography and other means if necessary due to noise and solvent impurites. Able to coordinate synthetic strategies with goal oriented team leaders as well as like minded coworkers. Organized with written observations and laboratory notes for peer-reviewed publications and data reporting as well as information retrieval and familiar with FDA GMP standards. Have thousands of examples of prior research spectra for inspection and verification of all referenced skill sets and am able to characterize many unknown molecular systems as well. EMPLOYMENT Associates of Cape Cod, Independent Contractor September 2009-September 2010 While contracting for ACC, I was responsible for the synthesis and spectroscopic analysis of several polypeptides for the furtherance of research into detection systems derived from the Limulus Horseshoe crab endotoxin and the resultant LAL clotting cascade. See http://www.acciusa.com for further information. Konarka Technologies, Independent Contractor January 2005-September 2005 A number of full and partial spectrum light absorbing conjugated hyphens were prepared using

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Page 1: Roger OConnor SOCcGMPRes 2016

3 R O U N D T R E E D R I V E , M E R R I MA C K , N H O 3 O 5 4

6 0 3 -3 4 1 -8 4 0 5 O R G O H I L E @G MA I L .C O M

ROGER O ’ CONNOR

SYNTHETIC ORGANIC CHEMIST

Focused and very precise experienced research chemist with nearly ten years experience

designing and completing synthetic methodologies from retrosynthetic analysis to endgame

and spectroscopic analysis and structure determination of natural products, analogues and

polypeptides. Also experienced with coordinating off-site syntheses and written/electronic

reports and research progress communication and very experienced with 1D and 2D NMR, FTIR

and ATR, HPLC, recycling HPLC and GCMS/LCMS.

FUNCTIONAL SUMMARY

Development of synthetic strategies as well as nearly 10 years experience as bench chemist

Experienced with 1H, 13C, 19F, 31P, HH-COSY, CH-COSY, NOESY, HMQC and other

experiments and analysis and precise data processing.

Purification of various sythetic samples through recrystallization, chromatography and other

means if necessary due to noise and solvent impurites.

Able to coordinate synthetic strategies with goal oriented team leaders as well as like

minded coworkers.

Organized with written observations and laboratory notes for peer-reviewed publications

and data reporting as well as information retrieval and familiar with FDA GMP standards.

Have thousands of examples of prior research spectra for inspection and verification of all

referenced skill sets and am able to characterize many unknown molecular systems as well.

EMPLOYMENT

Associates of Cape Cod, Independent Contractor September 2009-September 2010

While contracting for ACC, I was responsible for the synthesis and spectroscopic analysis of

several polypeptides for the furtherance of research into detection systems derived from the

Limulus Horseshoe crab endotoxin and the resultant LAL clotting cascade. See

http://www.acciusa.com for further information.

Konarka Technologies, Independent Contractor January 2005-September 2005

A number of full and partial spectrum light absorbing conjugated hyphens were prepared using

Page 2: Roger OConnor SOCcGMPRes 2016

a number of different catalytic methodologies, purified and characterized using various NMR

experiments as well as the standard spectroscopic means. This research was conducted

towards the development of innovative flexible organic dye-based photovoltaic cells and was

funded under numerous DARPA grants.

EDUCATION

Dartmouth College, PhD Candidate September 2005-July 2008

As a graduate researcher significant progress was made towards a novel total synthesis of the

naturally occurring anti-tumor compounds viridin and wortmannin. A number of significant

synthetic developments were achieved, most notably the development of a one-pot synthetic

methodology enabling a stereoselective synthesis of a model wortmannin compound This

included full NMR characterization using 1H, 13C, COSY, NOESY and HMQC techniques. Several

publications have been made based on this work over the last several years, in addition to

significant unpublished research.

University of Massachusetts Lowell BS, Chemistry September 2002-December 2004

As an undergraduate, research was conducted towards the development of a number of

antarafacial 2 + 2 ground state cycloadditions and further experimentation in attempts at

developing a ring opening/rearrangement cascade using metal hydrides as nucleophiles. While

these conditions proved viable only with highly strained ring systems it was a very instructive

lesson in the power of NMR technology in determining reaction products and structural analysis

as well as technical operation of the UNIX software and the instrumentation itself.

PUBLICATIONS

Constructing the Heterocyclic Core of Viridin and Wortmannin. Jacobi, P. A., Könekamp, T.,

Mascall, K.C., O’Connor, R.T., Onyango, E.O., Sessions, E.H.; Advances in Heterocyclic Chemistry

2013, 110(4), 119-143.

Mechanism of the decarboxylative rearrangement of β-(carbonyl)-

Cyclopropane carboxylic acids to 2-substituted-4,5-dihydrofurans.

Jahngen, E., Mallet, J., O’Connor, R.T., Jr., Fischer, S.; ARKIVOC 2007, 9,135-149.

Furanosteroid Studies. Stereoselective Synthesis of the A,B,E-Ring Core of Wortmannin.

Sessions, E.H., O’Connor, R.T., Jr., Jacobi, P.A.;Org. Lett. 2007, 9(17), 3221-3224. (Please see

supporting information for graphic representation of spectroscopic work).

REFERENCES

Edwin Jahngen

Professor of Chemistry

University of Massachusetts, Lowell

(603) 702-1389, (978) 934-3693,

Page 3: Roger OConnor SOCcGMPRes 2016

[email protected]

Scott Selfridge

Research Chemist

Akita Innovations, LLC

(603) 321-1008

[email protected]

Savvas Hadjikyriacou

Chemist

Equova Water Technologies

(978) 649-0528

[email protected]

Peter Jacobi

Professor of Chemistry

Dartmouth College

(603) 646-3495

[email protected]