Chiral Lewis Acid in Catalytic Asymmetric Reactions

13Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.

Abstract

Recent development in the field of asymmetric reactions has realized various efficient procedures to prepare highly optically active compounds by employing chiral Lewis acids. In this review are summarized the development of the chiral Lewis acids and the application to asymmetric reactions such as the Diels-Alder reaction, [2 + 2] cycloaddition reaction, alkylation reaction, hydrocyanation etc. Structures of the complexs between carbonyl compounds and Lewis acids are briefly discussed. © 1990, The Society of Synthetic Organic Chemistry, Japan. All rights reserved.

Cite

CITATION STYLE

APA

Hayashi, Y., & Narasaka, K. (1990). Chiral Lewis Acid in Catalytic Asymmetric Reactions. Journal of Synthetic Organic Chemistry, Japan, 48(4), 280–291. https://doi.org/10.5059/yukigoseikyokaishi.48.280

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free