Total Facial Discrimination of 1,3-Dipolar Cycloadditions in a d-Erythrose 1,3-Dioxane Template: Computational Studies of a Concerted Mechanism-Reference-Cited by-同舟云学术

Total Facial Discrimination of 1,3-Dipolar Cycloadditions in a d-Erythrose 1,3-Dioxane Template: Computational Studies of a Concerted Mechanism

Published:2017-01-09 Issue:2 Volume:82 Page:982-991
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sousa Cristina E. A.¹^ORCID,Ribeiro António M. P.¹,Gil Fortes António¹,Cerqueira Nuno M. F. S. A.²,Alves Maria J.¹^ORCID

Affiliation:

1. Departamento de Química, Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal

2. REQUIMTE/UCIBIO, Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua do Campo Alegre s/n, 4169-007 Porto, Portugal

Funder

European Regional Development Fund

Fundação para a Ciência e a Tecnologia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02518

Reference35 articles.

1. Stereoselective Approaches to Bioactive Carbohydrates and Alkaloids-With a Focus on Recent Syntheses Drawing from the Chiral Pool

2. Synthesis of Iminosugars from Tetroses

3. Synthesis of leukotriene A4 methyl ester from D-glucose

4. Synthese vonerythro-Sphingosinen über die Azidoderivate

5. Diastereo-controlled Diels–Alder cycloadditions of erythrose benzylidene-acetal 1,3-butadienes by 4-substituted-1,2,4-triazoline-3,5-dione: Evidence for the stereoelectronic effects on the dienes

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