"Organo-Metal" Synergistic Catalysis: The 1+1>2 Effect for the Construction of Spirocyclopentene Oxindoles

被引：69

作者：

Sun, Wangsheng ^{[1
,2
]}

Zhu, Gongming ^{[1
,2
]}

Wu, Chongyang ^{[1
,2
]}

Hong, Liang ^{[1
,2
]}

Wang, Rui ^{[1
,2
]}

机构：

[1] Lanzhou Univ, Key Lab Preclin Study New Drugs Gansu Prov, State Key Lab Appl Organ Chem, Sch Life Sci, Lanzhou 730000, Peoples R China

[2] Lanzhou Univ, Inst Biochem & Mol Biol, Sch Life Sci, Lanzhou 730000, Peoples R China

来源：

CHEMISTRY-A EUROPEAN JOURNAL | 2012年 / 18卷 / 44期

关键词：

aldehydes; enantioselectivity; oxindoles; spiro compounds; synergistic catalysis; HIGHLY ENANTIOSELECTIVE SYNTHESIS; BAYLIS-HILLMAN CARBONATES; STRUCTURE-BASED DESIGN; TRANSITION-METAL; 3+2 ANNULATION; QUATERNARY STEREOCENTERS; ASYMMETRIC CONSTRUCTION; CONCISE SYNTHESIS; SPIROOXINDOLES; COMBINATION;

D O I：

10.1002/chem.201201976

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

收藏

页码：13959 / 13963

页数：5

相关论文

共 73 条

[1] Assembly of Spirooxindole Derivatives Containing Four Consecutive Stereocenters via Organocatalytic Michael-Henry Cascade Reactions [J].

Albertshofer, Klaus ;

Tan, Bin ;

Barbas, Carlos F., III .

ORGANIC LETTERS, 2012, 14 (07) :1834-1837

[2] Synergistic catalysis: A powerful synthetic strategy for new reaction development [J].

Allen, Anna E. ;

MacMillan, David W. C. .

CHEMICAL SCIENCE, 2012, 3 (03) :633-658

[3]

[Anonymous], 2007, ANGEW CHEM, DOI DOI 10.1103/PHYSREVLETT.112.077206

[4] Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products [J].

Antonchick, Andrey P. ;

Gerding-Reimers, Claas ;

Catarinella, Mario ;

Schuermann, Markus ;

Preut, Hans ;

Ziegler, Slava ;

Rauh, Daniel ;

Waldmann, Herbert .

NATURE CHEMISTRY, 2010, 2 (09) :735-740

[5]

Bergonzini G., 2012, ANGEW CHEM, V124, P995

[6] Dioxindole in Asymmetric Catalytic Synthesis: Routes to Enantioenriched 3-Substituted 3-Hydroxyoxindoles and the Preparation of Maremycin A [J].

Bergonzini, Giulia ;

Melchiorre, Paolo .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2012, 51 (04) :971-974

[7] CYCLOPIAMINES-A AND CYCLOPIAMINES-B NOVEL OXINDOLE METABOLITES OF PENICILLIUM-CYCLOPIUM WESTLING [J].

BOND, RF ;

BOEYENS, JCA ;

HOLZAPFEL, CW ;

STEYN, PS .

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1979, (07) :1751-1761

[8]

Cao Y.-M., 2011, ANGEW CHEM, V123, P9290, DOI DOI 10.1002/ANGE.201104216

[9] Enantioselective Michael/Cyclization Reaction Sequence: Scaffold-Inspired Synthesis of Spirooxindoles with Multiple Stereocenters [J].

Cao, Yiming ;

Jiang, Xianxing ;

Liu, Luping ;

Shen, Fangfang ;

Zhang, Futing ;

Wang, Rui .

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (39) :9124-9127

[10] Organocatalytic Direct Asymmetric Aldol Reactions of 3-Isothiocyanato Oxindoles to Ketones: Stereocontrolled Synthesis of Spirooxindoles Bearing Highly Congested Contiguous Tetrasubstituted Stereocenters [J].

Chen, Wen-Bing ;

Wu, Zhi-Jun ;

Hu, Jing ;

Cun, Lin-Feng ;

Zhang, Xiao-Mei ;

Yuan, Wei-Cheng .

ORGANIC LETTERS, 2011, 13 (09) :2472-2475

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