Stereospecific C–S Bond Formation from Chiral Tertiary Alcohols by Quinone-Mediated Oxidation–Reduction Condensation Using Alkyl Diphenylphosphinites and Its Application to the Synthesis of a Chiral Tertiary Thiol

2006 ◽  
Vol 79 (5) ◽  
pp. 780-790 ◽  
Author(s):  
Kazuhiro Ikegai ◽  
Wanchai Pluempanupat ◽  
Teruaki Mukaiyama
2006 ◽  
Vol 35 (12) ◽  
pp. 1432-1433 ◽  
Author(s):  
Kiichi Kuroda ◽  
Nobuya Kaneko ◽  
Yujiro Hayashi ◽  
Teruaki Mukaiyama

ChemInform ◽  
2007 ◽  
Vol 38 (16) ◽  
Author(s):  
Kiichi Kuroda ◽  
Nobuya Kaneko ◽  
Yujiro Hayashi ◽  
Teruaki Mukaiyama

Author(s):  
Jie Jack Li ◽  
Chris Limberakis ◽  
Derek A. Pflum

Searching for reaction in organic synthesis has been made much easier in the current age of computer databases. However, the dilemma now is which procedure one selects among the ocean of choices. Especially for novices in the laboratory, it becomes a daunting task to decide what reaction conditions to experiment with first in order to have the best chance of success. This collection intends to serve as an "older and wiser lab-mate" one could have by compiling many of the most commonly used experimental procedures in organic synthesis. With chapters that cover such topics as functional group manipulations, oxidation, reduction, and carbon-carbon bond formation, Modern Organic Synthesis in the Laboratory will be useful for both graduate students and professors in organic chemistry and medicinal chemists in the pharmaceutical and agrochemical industries.


Author(s):  
ERNEST L. ELIEL ◽  
JORMA K. KOSKIMIES ◽  
BRUNO LOHRI ◽  
W. JACK FRAZEE ◽  
SUSAN MORRIS-NATSCHKE ◽  
...  

Synfacts ◽  
2006 ◽  
Vol 2006 (11) ◽  
pp. 1181-1181
Author(s):  
D. Ramón ◽  
M. Yus ◽  
V. Forrat

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