ChemInform Abstract: Asymmetric Synthesis of Quaternary Carbon Compounds via Chiral Bicyclic Lactams

ChemInform ◽  
2010 ◽  
Vol 26 (28) ◽  
pp. no-no
Author(s):  
A. I. MEYERS
1989 ◽  
Vol 54 (17) ◽  
pp. 4243-4246 ◽  
Author(s):  
A. I. Meyers ◽  
Bruce A. Lefker ◽  
Thomas J. Sowin ◽  
Larry J. Westrum

1960 ◽  
Vol 25 (5) ◽  
pp. 835-838 ◽  
Author(s):  
Franklin Prout ◽  
Bohdan Burachinsky ◽  
William Brannen, Jr. ◽  
Herbert Young

2015 ◽  
Vol 51 (2) ◽  
pp. 380-383 ◽  
Author(s):  
Masahiro Egi ◽  
Kaori Shimizu ◽  
Marin Kamiya ◽  
Yuya Ota ◽  
Shuji Akai

An asymmetric synthesis of highly substituted indenes has been developed via the central–axial–central chirality transfer from optically active propargyl alcohols.


Heterocycles ◽  
1996 ◽  
Vol 43 (5) ◽  
pp. 1031 ◽  
Author(s):  
Shunsaku Shiotani ◽  
Hirohiko Okada ◽  
Kumiko Nakamata ◽  
Takako Yamamoto ◽  
Fumie Sekino

Synlett ◽  
2018 ◽  
Vol 29 (20) ◽  
pp. 2601-2607 ◽  
Author(s):  
Jun-Long Li ◽  
Qing-Zhu Li ◽  
Yue Liu ◽  
Hai-Jun Leng

The construction of a chiral halogenated cyclic quaternary carbon center through various catalytic strategies is an emerging hot topic in the field of asymmetric synthesis. Herein, we give a summary of recently developed synthetic methods for preparing such structures. In addition, a novel enolate activation mode of aldehydes is highlighted, which provides an elegant pathway to access enantiopure heterocycles featuring a halogenated quaternary stereocenter through organocatalytic [4+2] cycloaddition.


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