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David A. Oare - Publications

Affiliations: 
Bioorganic Chemistry Genentech, Inc., San Francisco, CA, United States 
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14 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 OARE DA, HEATHCOCK CH. ChemInform Abstract: Acyclic Stereocontrol in Michael Addition Reactions of Enamines and Enol Ethers Cheminform. 22: no-no. DOI: 10.1002/chin.199132288  0.661
2007 Oare DA, Heathcock CH. Acyclic stereocontrol in Michael addition reactions of enamines and enol ethers Topics in Stereochemistry. 20: 87-170. DOI: 10.1002/9780470147290.Ch2  0.666
2007 Oare DA, Heathcock CH. Stereochemistry of the Base‐Promoted Michael Addition Reaction Topics in Stereochemistry. 19: 227-407. DOI: 10.1002/9780470147283.Ch5  0.646
1990 Oare DA, Heathcock CH. 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. DOI: 10.1021/Jo00288A028  0.523
1990 Oare DA, Henderson MA, Sanner MA, Heathcock CH. 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. DOI: 10.1021/Jo00288A027  0.483
1990 OARE DA, HENDERSON MA, SANNER MA, HEATHCOCK CH. 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. DOI: 10.1002/CHIN.199027099  0.335
1990 OARE DA, HEATHCOCK CH. ChemInform Abstract: Acyclic Stereoselection. Part 47. Stereochemistry of the Michael Addition of Ester and Ketone Enolates to α,β-Unsaturated Ketones. Cheminform. 21. DOI: 10.1002/chin.199027098  0.546
1989 OARE DA, HEATHCOCK CH. ChemInform Abstract: Synthesis of the Cyclic Hexapeptide Echinocandin D. New Approaches to the Asymmetric Synthesis of β-Hydroxy-α-amino Acids Cheminform. 20. DOI: 10.1002/chin.198916362  0.485
1987 Oare DA, Heathcock CH. Influence of enolate geometry on the stereochemistry of Michael additions of ketone enolates to α,β-unsaturated ketones Tetrahedron Letters. 28: 1354. DOI: 10.1016/S0040-4039(00)85424-6  0.571
1987 OARE DA, HEATHCOCK CH. 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. DOI: 10.1002/chin.198725063  0.543
1985 Heathcock CH, Oare DA. Acyclic stereoselection. 31. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enones Journal of Organic Chemistry. 50: 3022-3024. DOI: 10.1021/Jo00216A051  0.628
1985 Heathcock CH, Henderson MA, Oare DA, Sanner MA. Acyclic stereoselection. 30. Stereoselection in the Michael addition reaction. 2. Stereochemistry of the kinetic Michael reaction of amide enolates with enones The Journal of Organic Chemistry. 50: 3019-3022. DOI: 10.1021/Jo00216A050  0.553
1985 Heathcock CH, Oare DA. Acyclic Stereoselection. 31. Stereoselection In The Michael Addition Reaction. 3. Relationship Between Ester Enolate Geometry And Adduct Stereochemistry In The Kinetic Michael Reaction Of Lithium Enolates With Enones Cheminform. 16. DOI: 10.1002/Chin.198551087  0.672
1985 Heathcock CH, Oare DA. Stereoselection in the Michael addition reaction. 3. Relationship between ester enolate geometry and adduct stereochemistry in the kinetic Michael reaction of lithium enolates with enones Journal of Organic Chemistry. 50: 3022-3024.  0.658
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