Thermodynamically driven, syn-selective vinylogous aldol reaction of tetronamides-Reference-Cited by-同舟云学术

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Thermodynamically driven, syn-selective vinylogous aldol reaction of tetronamides

Published:2016 Issue:21 Volume:14 Page:4897-4907
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Karak Milandip¹²³⁴⁵,Barbosa Luiz C. A.¹²³⁴⁵,Acosta Jaime A. M.¹²³⁴⁵,Sarotti Ariel M.⁶⁷⁸⁹,Boukouvalas John¹⁰¹¹¹²¹³¹⁴

Affiliation:

1. Department of Chemistry

2. Instituto de Ciências Exatas

3. Universidade Federal de Minas Gerais

4. Belo Horizonte

5. Brazil

6. Instituto de Química Rosario (IQUIR)

7. Universidad Nacional de Rosario–CONICET

8. S2002LRK Rosario

9. Argentina

10. Département de Chimie

11. Pavillon Alexandre-Vachon

12. Université Laval

13. Quebec City

14. Canada

Abstract

A stereoselective vinylogous aldol reaction of N-monosubstituted tetronamides with aldehydes is described.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB00895J

Reference82 articles.

1. TFA-catalyzed ring transformation of 4-hydroxycyclobutenone: A simple and general route for preparation of 3-substituted 4-aminofuran-2(5H )-ones †

2. Conformationally Constrained β-Amino Acid Derivatives by Intramolecular [2 + 2]-Photocycloaddition of a Tetronic Acid Amide and Subsequent Lactone Ring Opening

3. Torquoselective 6π-Electron Electrocyclic Ring Closure of 1-Azatrienes Containing Acyclic Chirality at the C-Terminus

4. Reactivity of γ-Hydroxy-α,β-acetylenic Esters with Amines: Facile Synthesis of the Optically Active 4-Amino-2(5H)-furanones

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