Catalytic Asymmetric Formal [3+2] Cycloaddition of 2-Isocyanatomalonate Esters and Unsaturated Imines: Synthesis of Highly Substituted Chiral γ-Lactams-Reference-Cited by-同舟云学术

Catalytic Asymmetric Formal [3+2] Cycloaddition of 2-Isocyanatomalonate Esters and Unsaturated Imines: Synthesis of Highly Substituted Chiral γ-Lactams

Published:2017-09-21 Issue:59 Volume:23 Page:14707-14711
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Espinosa Miguel¹,Blay Gonzalo¹^ORCID,Cardona Luz¹^ORCID,Muñoz M. Carmen²,Pedro José R.¹^ORCID

Affiliation:

1. Departament de Química Orgànica, Facultat de Química; Universitat de València; C/ Dr. Moliner 50 46100 Burjassot Spain

2. Departament de Física Aplicada; Universitat Politècnica de València; Camí de Vera, S/N 46071 València Spain

Funder

Secretaría de Estado de Investigación, Desarrollo e Innovación

Generalitat Valenciana

Ministerio de Economía y Competitividad

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference122 articles.

1. The Practice of Ring Constraint in Peptidomimetics Using Bicyclic and Polycyclic Amino Acids

2. Pyroglutamic acid: a versatile building block in asymmetric synthesis

3. Pyroglutamic Acid Derivatives: Building Blocks for Drug Discovery

4. Synthesis and biological evaluation of (−)-kainic acid analogues as phospholipase D-coupled metabotropic glutamate receptor ligands

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