1981 - Fellow of Alfred P. Sloan Foundation
His scientific interests lie mostly in Organic chemistry, Aldehyde, Lewis acids and bases, Enantioselective synthesis and Catalysis. His study connects Medicinal chemistry and Organic chemistry. His study on Aldehyde is mostly dedicated to connecting different topics, such as Stereochemistry.
His biological study spans a wide range of topics, including Bryostatin, Bryostatins, Annulation and Bryostatin 1. His research in Lewis acids and bases intersects with topics in Addition reaction and Stereoselectivity. His study in Enantioselective synthesis is interdisciplinary in nature, drawing from both Titanium, Diels alder and Solvent.
His primary areas of investigation include Organic chemistry, Stereochemistry, Aldehyde, Bryostatin 1 and Catalysis. His work carried out in the field of Stereochemistry brings together such families of science as Bryostatins and Stereoselectivity. His Stereoselectivity study incorporates themes from Enantiomer and Medicinal chemistry.
His work in Aldehyde tackles topics such as Lewis acids and bases which are related to areas like Addition reaction, Nucleophile, Chelation and Stannane. Gary E. Keck combines subjects such as Bryostatin, Biological activity and Ring with his study of Bryostatin 1. His Catalysis study integrates concerns from other disciplines, such as Titanium and Combinatorial chemistry.
Gary E. Keck mainly investigates Protein kinase C, Bryostatin 1, Bryostatin, Biochemistry and Stereochemistry. His studies in Protein kinase C integrate themes in fields like Combinatorial chemistry, Leukemia and Tricyclic. His Bryostatin 1 research includes elements of Biological activity, Cancer research, LNCaP and Ring.
His Bryostatin research incorporates elements of U937 cell, Phorbol, PKC alpha and Protein kinase A. Within one scientific family, Gary E. Keck focuses on topics pertaining to Bryostatins under Stereochemistry, and may sometimes address concerns connected to Total synthesis. He interconnects Natural product, Aldehyde and Annulation in the investigation of issues within Pyran.
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Catalytic asymmetric allylation of aldehydes
Gary E. Keck;Kenneth H. Tarbet;Leo S. Geraci.
Journal of the American Chemical Society (1993)
Proton-transfer steps in Steglich esterification: a very practical new method for macrolactonization
Eugene P. Boden;Gary E. Keck.
Journal of Organic Chemistry (1985)
Carbon-carbon bond formation via the reaction of trialkylallylstannanes with organic halides
Gary E. Keck;John B. Yates.
Journal of the American Chemical Society (1982)
One electron C-C bond forming reactions via allylstannanes: scope and limitations
Gary E. Keck;Eric J. Enholm;John B. Yates;Michael R. Wiley.
PRONOUNCED SOLVENT AND CONCENTRATION EFFECTS IN AN ENANTIOSELECTIVE MUKAIYAMA ALDOL CONDENSATION USING BINOL-TITANIUM(IV) CATALYSTS
Gary E. Keck;Dhileepkumar Krishnamurthy.
Journal of the American Chemical Society (1995)
Stereochemical consequences for the Lewis acid mediated additions of allyl and crotyltri-n-butylstannane to chiral β-hydroxyaldehyde derivatives
Gary E. Keck;Duain E. Abbott.
Tetrahedron Letters (1984)
Catalytic Enantioselective Synthesis of Dihydropyrones via Formal Hetero Diels-Alder Reactions of "Danishefsky's Diene" with Aldehydes
Gary E. Keck;Xiang Yi Li;Dhileepkumar Krishnamurthy.
Journal of Organic Chemistry (1995)
Catalytic asymmetric allylation reactions. 3. Extension to methallylstannane, comparison of procedures, and observation of a nonlinear effect
Gary E. Keck;Dhileepkumar Krishnamurthy;Mark C. Grier.
Journal of Organic Chemistry (1993)
Total Synthesis of Bryostatin 1
Gary E. Keck;Yam B. Poudel;Thomas J. Cummins;Arnab Rudra.
Journal of the American Chemical Society (2011)
Catalytic asymmetric allylation (CAA) reactions. II. A new enantioselective allylation procedure
Gary E. Keck;Leo S. Geraci.
Tetrahedron Letters (1993)
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