Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates-Reference-Cited by-同舟云学术

Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates

Published:2015 Issue:27 Volume:13 Page:7393-7396
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

De Munck Lode¹²³⁴⁵,Monleón Alicia¹²³⁴⁵,Vila Carlos¹²³⁴⁵,Muñoz M. Carmen⁶⁷⁵,Pedro José R.¹²³⁴⁵

Affiliation:

1. Departament de Química Orgànica

2. Facultat de Química

3. Universitat de València

4. 46100 Burjassot

5. Spain

6. Departament de Física Aplicada

7. Universitat Politècnica de València

Abstract

An enantioselective alkynylation of cyclic benzoxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn(ii) complexes is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB01012H

Reference57 articles.

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5. Addition of Organometallic Reagents to Imines Bearing Stereogenic N-Substituents. Stereochemical Models Explaining the 1,3-Asymmetric Induction

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