ChemInform Abstract: L-Selectride-Mediated Highly Diastereoselective Asymmetric Reductive Aldol Reaction: Access to an Important Subunit for Bioactive Molecules.

ChemInform ◽  
2009 ◽  
Vol 40 (12) ◽  
Author(s):  
Arun K. Ghosh ◽  
Jorden Kass ◽  
David D. Anderson ◽  
Xiaoming Xu ◽  
Christine Marian
2008 ◽  
Vol 10 (21) ◽  
pp. 4811-4814 ◽  
Author(s):  
Arun K. Ghosh ◽  
Jorden Kass ◽  
David D. Anderson ◽  
Xiaoming Xu ◽  
Christine Marian

ChemInform ◽  
2009 ◽  
Vol 40 (39) ◽  
Author(s):  
Minoru Kato ◽  
Hiroshi Oki ◽  
Kenichi Ogata ◽  
Shin-ichi Fukuzawa

ChemInform ◽  
2004 ◽  
Vol 35 (13) ◽  
Author(s):  
Timothy J. Donohoe ◽  
David House ◽  
K. W. Ace

ChemInform ◽  
2012 ◽  
Vol 43 (46) ◽  
pp. no-no
Author(s):  
Kazuki Osakama ◽  
Masaharu Sugiura ◽  
Makoto Nakajima ◽  
Shunsuke Kotani

Author(s):  
Sivaparwathi Golla ◽  
Naveenkumar Anugu ◽  
Swathi Jalagam ◽  
Hari Prasad Kokatla

A transition-metal and hydride-free reductive aldol reaction has been developed for the synthesis of biologically active 3,3´-disubstituted oxindoles from isatin-derivatives using rongalite. In this protocol, rongalite plays the dual role...


2006 ◽  
Vol 8 (26) ◽  
pp. 5943-5946 ◽  
Author(s):  
Olivier Chuzel ◽  
Julia Deschamp ◽  
Christophe Chausteur ◽  
Olivier Riant

2000 ◽  
Vol 122 (18) ◽  
pp. 4528-4529 ◽  
Author(s):  
Steven J. Taylor ◽  
Matthew O. Duffey ◽  
James P. Morken

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