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Stereochemical and Skeletal Diversity Arising from Amino Propargylic Alcohols

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2883853.pdf (1.03 MB)

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2010

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10.1021/ol100914b

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American Chemical Society
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Pizzirani, Daniela, Taner Kaya, Paul A. Clemons, and Stuart L. Schreiber. 2010. Stereochemical and Skeletal Diversity Arising from Amino Propargylic Alcohols. Organic Letters 12(12): 2822-2825.

Abstract

An efficient synthetic pathway to the possible stereoisomers of skeletally diverse heterocyclic small molecules is presented. The change in shape brought about by different intramolecular cyclizations of diastereoisomeric amino propargylic alcohols is quantified using principal moment-of-inertia (PMI) shape analysis.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883853/pdf/

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http://nrs.harvard.edu/urn-3:HUL.InstRepos:4457725

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