Late-Stage Bromination Enables the Synthesis of Rubrolides B, I, K, and O-Reference-Cited by-同舟云学术

Late-Stage Bromination Enables the Synthesis of Rubrolides B, I, K, and O

Published:2016-07-06 Issue:22 Volume:2016 Page:3780-3787
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Karak Milandip¹²^ORCID,Acosta Jaime A. M.¹,Barbosa Luiz C. A.¹²^ORCID,Boukouvalas John¹³

Affiliation:

1. Department of Chemistry; Universidade Federal de Minas Gerais; Av. Pres. Antônio Carlos, 6627, Campus Pampulha CEP 31270-901 Belo Horizonte MG Brazil

2. Department of Chemistry; Universidade Federal de Viçosa; Av. Peter Henry Rolfs, s/n Campus Universitário CEP 36570-900 Viçosa MG Brazil

3. Department of Chemistry; Université Laval; Pavillon Alexandre-Vachon, 1045 Avenue de la Médecine G1V 0A6 Quebec City, Quebec Canada

Funder

National Council for Scientific and Technological Development

Foundation for Research Support of the State of Minas Gerais

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference57 articles.

1. Furanolate-based strategy for sequential 2,3,4-trisubstitution of butenolide: Total synthesis of nostoclides I and II

2. Synthetic Applications of 3,4-Dihalo-2(5H)-furanones: A Formal Total Synthesis of Nostoclides I and II

3. Short and Efficient Synthesis of Cadiolide B

4. Synthesis of naturally occurring bioactive butyrolactones: maculalactones A–C and nostoclide I

5. A Unified Strategy for the Regiospecific Assembly of Homoallyl-Substituted Butenolides and γ-Hydroxybutenolides: First Synthesis of Luffariellolide

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