Highly Stereoselective C-Allylation of an Enantiopure α-Sulfinyl Thioacetamide-Reference-Cited by-同舟云学术

Highly Stereoselective C-Allylation of an Enantiopure α-Sulfinyl Thioacetamide

Published:2002-08-29 Issue:19 Volume:67 Page:6852-6855
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nowaczyk Stéphanie¹,Alayrac Carole¹,Metzner Patrick¹,Averbuch-Pouchot Marie-Thérèse¹

Affiliation:

1. Laboratoire de Chimie Moléculaire et Thio-organique (UMR CNRS 6507), ISMRA-Université de Caen, 6 Boulevard du Maréchal Juin, F-14050 Caen, France, and LEDSS (UMR CNRS 5616), Université Joseph Fourier, BP 53, F-38041 Grenoble, France patrick.metzner@ismra.fr

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0258610

Reference15 articles.

1. Optically Active t-Butyl 2-(p-Tolylsulfinyl)propionate and -butyrate: Synthesis and Reactivity in Aldol-type Condensations

2. Garcia Ruano, J. L.; Rumbero, A.Tetrahedron: Asymmetry1999,10, 4427−4436.

3. Asymmetric Thio-Claisen Rearrangement Induced by an Enantiopure Alkylsulfinyl Group. Unusual Preference for a Boat Transition State in the Acyclic Series

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