<--- Back to Details
First PageDocument Content
Diels–Alder reaction / Organocatalysis / Radical cyclization / Alkyne / Total synthesis / Endiandric acid C / Strychnine total synthesis / Chemistry / Organic reactions / Cycloaddition
Date: 2010-10-27 21:27:55
Diels–Alder reaction
Organocatalysis
Radical cyclization
Alkyne
Total synthesis
Endiandric acid C
Strychnine total synthesis
Chemistry
Organic reactions
Cycloaddition

Published on Web[removed]Nine-Step Enantioselective Total Synthesis of (+)-Minfiensine Spencer B. Jones, Bryon Simmons, and David W. C. MacMillan* Merck Center for Catalysis at Princeton UniVersity, Princeton, New Je

Add to Reading List

Source URL: www.princeton.edu

Download Document from Source Website

File Size: 404,90 KB

Share Document on Facebook

Similar Documents

PDF Document

DocID: 17nej - View Document

Acc. Chem. Res. 2000, 33, Hypersensitive Radical Probes and the Mechanisms of Cytochrome P450-Catalyzed Hydroxylation Reactions

Acc. Chem. Res. 2000, 33, Hypersensitive Radical Probes and the Mechanisms of Cytochrome P450-Catalyzed Hydroxylation Reactions

DocID: 13MqP - View Document

J. Org. Chem. 1998, 63, Picosecond Radical Kinetics. Fast Ring Openings of Secondary and Tertiary

J. Org. Chem. 1998, 63, Picosecond Radical Kinetics. Fast Ring Openings of Secondary and Tertiary

DocID: 13LaX - View Document

Published on Web[removed]Nine-Step Enantioselective Total Synthesis of (+)-Minfiensine Spencer B. Jones, Bryon Simmons, and David W. C. MacMillan* Merck Center for Catalysis at Princeton UniVersity, Princeton, New Je

Published on Web[removed]Nine-Step Enantioselective Total Synthesis of (+)-Minfiensine Spencer B. Jones, Bryon Simmons, and David W. C. MacMillan* Merck Center for Catalysis at Princeton UniVersity, Princeton, New Je

DocID: ECSA - View Document

C  View Online Chemical Science

C View Online Chemical Science

DocID: Eu9d - View Document