Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/96126
Title: Formal [4 + 1]- and [5 + 1]-annulation by an SN2–conjugate addition sequence : stereoselective synthesis of highly substituted carbocycles
Authors: Heng, Yi Li
Chiba, Shunsuke
Tong, Benny Meng Kiat
Chen, Hui
Chong, Sin Yee
Issue Date: 2012
Source: Tong, B. M. K., Chen, H., Chong, S. Y., Heng, Y. L., & Chiba, S. (2012). Formal [4 + 1]- and [5 + 1]-Annulation by an SN2–Conjugate Addition Sequence: Stereoselective Synthesis of Highly Substituted Carbocycles. Organic Letters, 14(11), 2826-2829.
Series/Report no.: Organic letters
Abstract: K2CO3-mediated reactions of 6-bromo-2-hexenoates and 7-bromo-2-heptenoate with active methylene compounds deliver highly substituted cyclopentane and cyclohexane derivatives, respectively via a sequence of SN2–conjugate addition reactions (formal [4 + 1]- and [5 + 1]-annulation) in a diastereoselective manner.
URI: https://hdl.handle.net/10356/96126
http://hdl.handle.net/10220/10606
ISSN: 1523-7060
DOI: 10.1021/ol301044e
Rights: © 2012 American Chemical Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

SCOPUSTM   
Citations 20

11
checked on Aug 31, 2020

WEB OF SCIENCETM
Citations 50

11
checked on Sep 17, 2020

Page view(s) 50

402
checked on Sep 24, 2020

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.