Literature DB >> 24918864

Highly regio- and stereoselective synthesis of alkylidenecyclopropanes via Ru(II)-Pheox catalyzed asymmetric inter- and intramolecular cyclopropanation of allenes.

Soda Chanthamath1, Hao Wei Chua, Seiya Kimura, Kazutaka Shibatomi, Seiji Iwasa.   

Abstract

An efficient protocol for the synthesis of optically active alkylidenecyclopropanes (ACPs) via the Ru(II)-Pheox catalyzed asymmetric cyclopropanation of allenes has been established. This catalytic system proceeded with high regioselectivity to give the ACP products in high yield with high diastereoselectivity (up to 99/1) and enantioselectivity (up to 99% ee).

Entities:  

Year:  2014        PMID: 24918864     DOI: 10.1021/ol5014944

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Highly stereoselective spirocyclopropanation of various diazooxindoles with olefins catalyzed using Ru(ii)-complex.

Authors:  Masaya Tone; Yoko Nakagawa; Soda Chanthamath; Ikuhide Fujisawa; Naofumi Nakayama; Hitoshi Goto; Kazutaka Shibatomi; Seiji Iwasa
Journal:  RSC Adv       Date:  2018-11-28       Impact factor: 3.361

  1 in total

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