Exploring the Aldol Reaction in the Synthesis of B... - BV FAPESP
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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Exploring the Aldol Reaction in the Synthesis of Bioactive Compounds

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Author(s):
Ferreira, Marco A. B. [1] ; Dias, Luiz C. [2] ; Leonarczyk, Ives A. [1] ; Polo, Ellen C. [2] ; de Lucca, Jr., Emilio C. [2]
Total Authors: 5
Affiliation:
[1] Univ Fed Sao Carlos, Dept Chem, BR-13560 Sao Carlos, SP - Brazil
[2] Univ Estadual Campinas, Inst Chem, BR-13083970 Campinas, SP - Brazil
Total Affiliations: 2
Document type: Journal article
Source: CURRENT ORGANIC SYNTHESIS; v. 12, n. 5, p. 547-564, 2015.
Web of Science Citations: 6
Abstract

Carbonyl chemistry, specifically aldol reactions, is one of the most efficient and elegant strategies to build carbon-carbon bonds. In the last 15 years in Brazil, our research group and others have worked on the development and application of stereoselective aldol reactions, with direct application in the asymmetric synthesis of several natural products of biological interest. In this review, we highlight the major Brazilian contributions to this field. (AU)

FAPESP's process: 11/06722-2 - Total synthesis of nhatrangins A and B
Grantee:Ellen Christine Polo
Support Opportunities: Scholarships in Brazil - Doctorate
FAPESP's process: 11/06721-6 - Total synthesis of marinisporolide A
Grantee:Emílio Carlos de Lucca Júnior
Support Opportunities: Scholarships in Brazil - Doctorate
FAPESP's process: 13/02311-3 - New approaches in asymmetric synthesis of tetrahydrofuran and tetrahydropyran-derivatives with potential application in the preparation of bioactive molecules
Grantee:Marco Antonio Barbosa Ferreira
Support Opportunities: Regular Research Grants
FAPESP's process: 12/02230-0 - Total synthesis of bioactive compounds: biological tests and design of new analogs
Grantee:Luiz Carlos Dias
Support Opportunities: Regular Research Grants