Recent Advances in Asymmetric Synthesis of Optically Active Indole Derivatives from 3-Indolylmethanols

2016 ◽  
Vol 36 (6) ◽  
pp. 1229 ◽  
Author(s):  
Shuai Zhu ◽  
Lubin Xu ◽  
Liang Wang ◽  
Jian Xiao
Synlett ◽  
2021 ◽  
Author(s):  
Memg Wang ◽  
Changxu Zhong ◽  
Ping Lu

Enantioselective synthesis of cyclobutane derivatives is still a challenging topic in asymmetric synthesis. [2+2]-Cycloaddition and skeleton rearrangement are two primary strategies to this end. Recently, functionalization of cyclobutanones and cyclobutenones, which are readily available via [2+2]-cycloadditions as prochiral substrates, has emerged as a powerful tool to access versatile four-membered ring compounds. Herein, we summarize some recent advances in these areas from our and other groups.


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.


Tetrahedron ◽  
2009 ◽  
Vol 65 (10) ◽  
pp. 1995-2004 ◽  
Author(s):  
Sara Pellegrino ◽  
Francesca Clerici ◽  
Alessandro Contini ◽  
Samantha Leone ◽  
Tullio Pilati ◽  
...  

2018 ◽  
Vol 16 (4) ◽  
pp. 510-520 ◽  
Author(s):  
Niankai Fu ◽  
Long Zhang ◽  
Sanzhong Luo

Recent advances in catalytic enantioselective enamine protonation for the synthesis of optically active carbonyl compounds are summarized in this review.


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

Sign in / Sign up

Export Citation Format

Share Document