|
||||||||||||||||
|
||||||||||||||||
The following HTML text is provided to enhance online readability. Many aspects of typography translate only awkwardly to HTML. Please use the page image as the authoritative form to ensure accuracy. 1977 The Nonclassical Ion Problem (with comments by P. von Schleyer). New York: Plenum Press. 1979 With S. Krishnamurthy. 40 years of hydride reductions. Tetrahedron 35:567-607. 1983 With P. K. Jadhav. Asymmetric carbon-carbon bond formation via B-allyldiisopinocampheylborane. A simple synthesis of secondary homoallylic alcohols with excellent enantiomeric purities. J. Am. Chem. Soc. 105:2092-2093. 1985 With T. Imai, M. C. Desai, and B. Singaram. Chiral synthesis via organoboranes. 3. Conversion of boronic esters of essentially 100-percent optical purity to aldehydes, acids, and homologated alcohols of very high enantiomeric purities. J. Am. Chem. Soc. 107:4980-4983. 1986 With K. S. Bhat. Enantiomeric (Z)- and (E)-crotyldiisopinocamphenylboranes. Synthesis in high optical purity of all four possible stereoisomers of β-methylhomoallyl alcohols. J. Am. Chem. Soc. 108:293-294. With K. W. Kim, T. E. Cole, and B. Singaram. Chiral synthesis via organoboranes. 8. Synthetic utility of boronic esters of essentially 100-percent optical purity—synthesis of primary amines of very high enantiomeric purities. J. Am. Chem. Soc. 108:6761-6764. 1988 With J. Chandrasekharan and P. V. Ramachandran. Chiral synthesis via organoboranes. 14. Selective reductions. 41. Diisopinocamphenylchloroborane. An exceptionally efficient chiral reducing agent. J. Am. Chem. Soc. 110:1539-1546. With B. Singaram. Development of a simple general procedure for synthesis of pure enantiomers via chiral organoboranes. Accounts Chem. Res. 21:287-293.
|
|
|||||||||||||||
