Spiro[pyrrolidine-2,3′-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-02

AUTHORS

Gang Chen, Jing Yang, Suo Gao, Hongping He, Shunlin Li, Yingtong Di, Ying Chang, Yang Lu, Xiaojiang Hao

ABSTRACT

A series of spiro-oxindole derivatives was synthesized by novel regioselective 1,3-dipolar cycloadditions of isatin, α-amino acids, and (E)-β-aryl-nitro-olefins. Regioisomers were produced in each reaction and the major products showed different regioselectivity compared to previously reported spiro-oxindole derivatives.

PAGES

151-156

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11030-011-9342-1

DOI

http://dx.doi.org/10.1007/s11030-011-9342-1

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1047991126

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/22134725


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