Fast & easy preparation of 3D scaffolds from methyl benzoate by a diversity oriented synthesis strategy based on Diels–Alder and ene-reactions-Reference-Cited by-同舟云学术

Fast & easy preparation of 3D scaffolds from methyl benzoate by a diversity oriented synthesis strategy based on Diels–Alder and ene-reactions

Published:2017 Issue:26 Volume:15 Page:5585-5592
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Brossard Dominique¹²³⁴⁵,Retailleau Pascal¹²³⁴⁵^ORCID,Dumontet Vincent¹²³⁴⁵,Breton Philippe⁶⁷⁵,Desrat Sandy¹²³⁴⁵^ORCID,Roussi Fanny¹²³⁴⁵^ORCID

Affiliation:

1. Institut de Chimie des Substances Naturelles

2. CNRS UPR 2301

3. Université Paris-Saclay

4. 91198 Gif-sur-Yvette

5. France

6. Institut de Recherche Servier

7. 78290 Croissy-sur-Seine

Abstract

Thermic dimerization of methyl 1,3-cyclohexadiene 2-carboxylate gave original 3D-shape compounds by Diels–Alder cycloaddition and original [6 + 4]-ene reaction.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01236E

Reference33 articles.

1. Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules

2. What Do Medicinal Chemists Actually Make? A 50-Year Retrospective

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4. Structural Diversity of Organic Chemistry. A Scaffold Analysis of the CAS Registry

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