Asymmetric synthesis of optically active 6-thiaestrogens

2010 ◽  
Vol 91 (7) ◽  
pp. 861-868 ◽  
Author(s):  
W. M. B. Könst ◽  
W. N. Speckamp ◽  
H. O. Houwen ◽  
H. O. Huisman
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.


1980 ◽  
Vol 333 (1 Transition Me) ◽  
pp. 35-44 ◽  
Author(s):  
J. K. Stille ◽  
S. J. Fritschel ◽  
N. Takaishi ◽  
T. Masuda ◽  
H. Imai ◽  
...  

1988 ◽  
Vol 52 (12) ◽  
pp. 3087-3092 ◽  
Author(s):  
Yukio YAMAMOTO ◽  
Kazuyoshi YAMAMOTO ◽  
Takaaki NISHIOKA ◽  
Jun''ichi ODA

2015 ◽  
Vol 51 (87) ◽  
pp. 15788-15791 ◽  
Author(s):  
Chandra M. R. Volla ◽  
Eleonora Fava ◽  
Iuliana Atodiresei ◽  
Magnus Rueping

A dual catalytic system consisting of indium triflate and a chiral imidazolidinone catalyzes the asymmetric addition of aldehydes to N-acyl quinoliniums furnishing optically active dihydroquinolines in good yields and excellent selectivities.


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