Michael G. Yang
Bristol-Myers Squibb (United States)(US)
Publications by Year
Research Areas
Asymmetric Synthesis and Catalysis, Synthetic Organic Chemistry Methods, Chemical Synthesis and Analysis, Crystallization and Solubility Studies, X-ray Diffraction in Crystallography
Most-Cited Works
- → A Stereochemical Model for Merged 1,2- and 1,3-Asymmetric Induction in Diastereoselective Mukaiyama Aldol Addition Reactions and Related Processes(1996)298 cited
- → Structure-based design of an osteoclast-selective, nonpeptide Src homology 2 inhibitor with in vivo antiresorptive activity(2000)133 cited
- → The Exceptional Chelating Ability of Dimethylaluminum Chloride and Methylaluminum Dichloride. The Merged Stereochemical Impact of α- and β-Stereocenters in Chelate-Controlled Carbonyl Addition Reactions with Enolsilane and Hydride Nucleophiles(2001)133 cited
- → Diastereoselective additions of chiral (E)-crotylsilanes to .alpha.-alkoxy and .beta.-alkoxy aldehydes. A one-step, silicon-directed tetrahydrofuran synthesis(1991)108 cited
- → Total Synthesis of (+)-Mycotrienol and (+)-Mycotrienin I: Application of Asymmetric Crotylsilane Bond Constructions(1998)78 cited
- → Diastereofacial selectivity with optically active .alpha.-substituted .beta.-silyl-(E)-hexenoates. Enantioselective construction of homoallylic ethers via reaction with aryl acetals(1991)71 cited
- → The Amyloid-β Rise and γ-Secretase Inhibitor Potency Depend on the Level of Substrate Expression(2008)66 cited
- → Diastereoselective Aldol and Allylstannane Addition Reactions. The Merged Stereochemical Impact of .alpha. and .beta. Aldehyde Substituents(1995)66 cited
- → Src Homology-2 Inhibitors: Peptidomimetic and Nonpeptide(2002)58 cited
- → Double stereodifferentiating Lewis acid-promoted (Mukaiyama) aldol bond constructions.(1995)55 cited