David A. Oare

Affiliations: 
Bioorganic Chemistry Genentech, Inc., San Francisco, CA, United States 
Google:
"David Oare"
Bio:

https://books.google.com/books?id=xupGAQAAMAAJ

Mean distance: (not calculated yet)
 

Parents

Sign in to add mentor
Clayton H. Heathcock grad student 1988 UC Berkeley
 (The stereochemistry of the Enolate Michael Addition)

Children

Sign in to add trainee
Derek S. Tan research assistant 1995-1995 Genentech, Inc.
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

OARE DA, HEATHCOCK CH. (2010) ChemInform Abstract: Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol Ethers Cheminform. 22: no-no
Oare DA, Heathcock CH. (2007) Acyclic stereocontrol in Michael addition reactions of enamines and enol ethers Topics in Stereochemistry. 20: 87-170
Oare DA, Heathcock CH. (2007) Stereochemistry of the Base‐Promoted Michael Addition Reaction Topics in Stereochemistry. 19: 227-407
Oare DA, Heathcock CH. (1990) Acyclic stereoselection. 47. Stereochemistry of the Michael addition of ester and ketone enolates to .alpha.,.beta.-unsaturated ketones The Journal of Organic Chemistry. 55: 157-172
Oare DA, Henderson MA, Sanner MA, et al. (1990) Acyclic stereoselection. 46. Stereochemistry of the Michael addition of N,N-disubstituted amide and thioamide enolates to .alpha.,.beta.-unsaturated ketones The Journal of Organic Chemistry. 55: 132-157
OARE DA, HENDERSON MA, SANNER MA, et al. (1990) ChemInform Abstract: Acyclic Stereoselection. Part 46. Stereochemistry of the Michael Addition of N,N-Disubstituted Amide and Thioamide Enolates to α,β-Unsaturated Ketones. Cheminform. 21
OARE DA, HEATHCOCK CH. (1990) ChemInform Abstract: Acyclic Stereoselection. Part 47. Stereochemistry of the Michael Addition of Ester and Ketone Enolates to α,β-Unsaturated Ketones. Cheminform. 21
OARE DA, HEATHCOCK CH. (1989) ChemInform Abstract: Synthesis of the Cyclic Hexapeptide Echinocandin D. New Approaches to the Asymmetric Synthesis of β-Hydroxy-α-amino Acids Cheminform. 20
Oare DA, Heathcock CH. (1987) Influence of enolate geometry on the stereochemistry of Michael additions of ketone enolates to α,β-unsaturated ketones Tetrahedron Letters. 28: 1354
OARE DA, HEATHCOCK CH. (1987) ChemInform Abstract: Acyclic Stereoselection. Part 38. Influence of Enolate Geometry on the Stereochemistry of Michael Additions of Ketone Enolates to α,β-Unsaturated Ketones. Cheminform. 18
See more...