Highly Stereoselective [3+2] Cycloadditions of Chiral Palladium-ContainingN1-1,3-Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles-Reference-Cited by-同舟云学术

Highly Stereoselective [3+2] Cycloadditions of Chiral Palladium-ContainingN1-1,3-Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles

Published:2016-03-18 Issue:18 Volume:22 Page:6243-6247
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Li Tian-Ren¹,Cheng Bei-Yi¹,Fan Si-Qi²,Wang Ya-Ni¹,Lu Liang-Qiu¹,Xiao Wen-Jing¹³

Affiliation:

1. CCNU-uOttawa Joint Research Centre, Key Laboratory of Pesticides and Chemical Biology; Ministry of Education; College of Chemistry; Central China Normal University; 152 Luoyu Road Wuhan, Hubei 430079 P. R. China

2. Department of Chemistry; University of Oregon; 1585 E 13th Ave. Eugene OR 97403 USA

3. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin 300072 P. R. China

Funder

Natural Science Foundation of China

Foundation for the Author of National Excellent Doctoral Dissertation of China

Outstanding Youth Funding in Hubei Province

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201600735/fullpdf

Reference87 articles.

1. Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products

2. Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position

3. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks

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