Spiro[pyrrolidine-2,3′-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions-Reference-Cited by-同舟云学术

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

Published:2011-12-02 Issue:1 Volume:16 Page:151-156
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

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

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

http://link.springer.com/content/pdf/10.1007/s11030-011-9342-1.pdf

Reference10 articles.

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2. Stanley R, Jan B, Birgitta S (2004) The three-component reaction between isatin, α-amino acids and dipolarophiles. Eur J Org Chem 2: 413–418. doi: 10.1002/ejoc.200300621

3. Abdel-Aziz S El-Ahl (2002) Three-component 1,3-dipolar cycloaddition reactions in synthesis of spiro [pyrrolidine-2,3′-oxindoline] derivatives. Heteroatom Chem 13:324–329. doi: 10.1002/hc.10038

4. Demosthenes F, William JR, David SC, David LC (1998) Solution phase synthesis of a spiro [pyrrolidine-2,3′-oxindole] library via a three component 1,3-dipolar cycloaddition reaction. Tetrahedron Lett 39: 2235–2238. doi: 10.1016/S0040-4039(98)00234-2

5. Rathna DRSM, Jayadevan JS, Selva K, Raghavachary RR (2006) A novel entry to dispiropyrrolo-bicyclo[2.2.1]heptanes through sequential 1,3-dipolar and Diels-Alder cycloaddition reactions. Tetrahedron Lett 47: 829–832. doi: 10.1016/j.tetlet.2005.11.089

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