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 - David MacMillan - Document - PDFSEARCH.IO

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	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 Document Date: 2010-10-27 21:27:55 Open Document File Size: 404,90 KB Share Result on Facebook City Dounay / Austin / / Company Boc / Merck / MacMillan / Bristol-Myers Squibb / Amgen / / Country France / United States / / Currency pence / USD / / / Facility Princeton UniVersity / / Holiday Padwa / / IndustryTerm natural product / isolation product / asymmetric protocol / acetylenic / / Organization David W. C. MacMillan* Merck Center for Catalysis / Princeton UniVersity / / Person Bryon Simmons / Spencer B. Jones / Sha / / Position rt / A. D. J. / / ProvinceOrState A. B. / / PublishedMedium Synlett / / RadioStation JA906472M J. AM / 9 J. AM / / Technology condensation / / URL http / SocialTag 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 JeAdd to Reading List