E,Z-Stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama–Michael addition-Reference-Cited by-同舟云学术

E,Z-Stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama–Michael addition

Published:2016 Issue:19 Volume:6 Page:15655-15659
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Espinosa Miguel¹²³⁴⁵,García-Ortiz Andrea¹²³⁴⁵,Blay Gonzalo¹²³⁴⁵,Cardona Luz¹²³⁴⁵,Muñoz M. Carmen⁶⁷⁸⁵,Pedro José R.¹²³⁴⁵

Affiliation:

1. Departament de Química Orgànica

2. Facultat de Química

3. Universitat de València

4. E-46100 Burjassot

5. Spain

6. Departament de Física Aplicada

7. Universitat Politècnica de València

8. 46022 València

Abstract

E or Z dehydroamino esters are stereoselectively obtained from a same set of reactants depending on the reaction conditions.

Funder

Secretaría de Estado de Investigación, Desarrollo e Innovación

Generalitat Valenciana

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/RA/C5RA27354D

Reference62 articles.

1. U. Kazmaier , Synthesis and Chemistry of α,β-Didehydroamino Acids, in Amino Acids, Peptides and Proteins in Organic Chemistry, ed. A. B. Andrew, Wiley-VCH, Weinheim, Germany, 2009, vol. 2, p. 3

2. Conformational study of poly-ΔAbu peptides and construction of amphipathic nanostructure

3. Recent Developments in Depsipeptide Research

4. Chemistry and Biology of Cyclic Depsipeptides of Medicinal and Biological Interest

5. Asymmetric Catalysis in Water: Prospects and Problems of Using Hydroxyphosphines and Hydroxyphosphinites as Ligands

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