ChemInform Abstract: CHIRAL QUATERNARY CARBON COMPOUNDS. II. AN ASYMMETRIC SYNTHESIS OF (R)- OR (S)-4,4-DIALKYL-2-CYCLOPENTENONES

1985 ◽  
Vol 16 (32) ◽  
Author(s):  
A. I. MEYERS ◽  
K. TH. WANNER
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.


ChemInform ◽  
2013 ◽  
Vol 44 (3) ◽  
pp. no-no
Author(s):  
Ryo Shintani ◽  
Tomoaki Ito ◽  
Midori Nagamoto ◽  
Haruka Otomo ◽  
Tamio Hayashi

Sign in / Sign up

Export Citation Format

Share Document