☆ 4.6 Article

Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles

CHEMISTRY-A EUROPEAN JOURNAL (2012)

Journal

CHEMISTRY-A EUROPEAN JOURNAL

Volume 18, Issue 1, Pages 63-67

Publisher

WILEY-V C H VERLAG GMBH

DOI: 10.1002/chem.201103449

Keywords

3; 3'-pyrrolidonyl spirooxindoles; cycloaddition; methyleneindolinones; organocatalysis; spiro compounds

Funding

Hangzhou Normal University in China, the Ministry of Education in Singapore [ARC12/07, T206B3225]
Skaggs Institute for Chemical Biology

Ask authors/readers for more resources

Protocol

Community support

Reagent

Community support

Authors

I am an author on this paper

Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6

Not enough ratings

Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles

Journal

CHEMISTRY-A EUROPEAN JOURNAL

Publisher

WILEY-V C H VERLAG GMBH

Keywords

Categories

Funding

Ask authors/readers for more resources

Protocol

Reagent

Authors

I am an author on this paper

Reviews

Primary Rating

Secondary Ratings

Novelty

Significance

Scientific rigor

Rate this paper

Recommended

Core Structure-Based Design of Organocatalytic [3+2]-Cycloaddition Reactions: Highly Efficient and Stereocontrolled Syntheses of 3,3′-Pyrrolidonyl Spirooxindoles

Journal

CHEMISTRY-A EUROPEAN JOURNAL

Publisher

WILEY-V C H VERLAG GMBH

Keywords

Categories

Funding

Ask authors/readers for more resources

Protocol

Reagent

Authors

I am an author on this paper

Reviews

Primary Rating

Secondary Ratings

Novelty

Significance

Scientific rigor

Rate this paper

Recommended

Export Citation

Share Paper