Inter-And intramolecular enantioselective carbolithiation reactions

32Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.

Abstract

In this review we summarize recent developments in inter- and intramolecular enantioselective carbolithiation reactions carried out in the presence of a chiral ligand for lithium, such as (-)-sparteine, to promote facial selection on a C=C bond. This is an attractive approach for the construction of new carbon-carbon bonds in an asymmetric fashion, with the possibility of introducing further functionalization on the molecule by trapping the reactive organolithium intermediates with electrophiles. © 2013 Gómez-SanJuan et al.

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Gómez-SanJuan, A., Sotomayor, N., & Lete, E. (2013, February 13). Inter-And intramolecular enantioselective carbolithiation reactions. Beilstein Journal of Organic Chemistry. https://doi.org/10.3762/bjoc.9.36

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 7

70%

Researcher 2

20%

Professor / Associate Prof. 1

10%

Readers' Discipline

Tooltip

Chemistry 13

100%

Save time finding and organizing research with Mendeley

Sign up for free