Microwave-Assisted Synthesis of beta-1,2,3-Triazolyl-alpha-amino Esters

Khan, Amna N.; Vasconcelos, Stanley N. S.; Carrau, Gonzalo; Stefani, Helio A.

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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.)

Microwave-Assisted Synthesis of beta-1,2,3-Triazolyl-alpha-amino Esters

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Author(s):	Khan, Amna N. ^[1] ; Vasconcelos, Stanley N. S. ^[1] ; Carrau, Gonzalo ^[1] ; Stefani, Helio A. ^[1] Total Authors: 4
Affiliation:	^[1] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, BR-05508000 Sao Paulo, SP - Brazil Total Affiliations: 1
Document type:	Journal article
Source:	Journal of the Brazilian Chemical Society; v. 26, n. 7, p. 1457-1465, JUL 2015.
Web of Science Citations:	1
Abstract
The reaction of ethyl (p-methoxyphenylimino) acetate with propargyl bromide mediated by activated zinc powder afforded alkynyl amine, which was then reacted with a variety of organic azides using a microwave energy source, leading to beta-1,2,3-triazolyl-alpha-amino esters in good yield. (AU)

FAPESP's process:	12/00424-2 - Synthesis of small libraries using potassium Organotrifluoroborates in Suzuki-Miyaura reactions
Grantee:	Helio Alexandre Stefani
Support Opportunities:	Research Projects - Thematic Grants

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