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Synthesis of N-substituted Pyrrolin-2-ones

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Date Issued:
1996
Title: Synthesis of N-substituted Pyrrolin-2-ones.
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Name(s): Mattern, R.-H., creator
Harbor Branch Oceanographic Institute
Type of Resource: text
Genre: Article
Issuance: single unit
Date Issued: 1996
Publisher: Elsevier B.V.
Extent: 5 p.
Physical Description: pdf
Language(s): English
Identifier: 3331910 (digitool), FADT3331910 (IID), fau:6149 (fedora), 10.1016/0040-4039(95)02267-8 (doi)
Note(s): During studies towards the synthesis of microcolin analogues, an unexpected dehydration was observed when 1-benzyloxycarbonyl-4-hydroxy-5-methylpyrrolidin-2-one was treated with di-tert-butyl dicarbonate in the presence of 4-dimethylaminopyridine. This reaction was used for the stereospecific synthesis of several N-protected pyrrolin-2-ones. The elimination of β-hydroxyl groups in 4-hydroxy-pyrrolidinones with di-tert-butyl dicarbonate is described.
This manuscript is an author version with the final publication available at http://www.sciencedirect.com/science/journal/00404039 and may be cited as: Mattern, R.-H. (1996). Synthesis of N-substituted Pyrrolin-2-ones. Tetrahedron Letters, 37(3), 291-294. doi:10.1016/0040-4039(95)02267-8
Florida Atlantic University. Harbor Branch Oceanographic Institute contribution #1119.
Subject(s): Stereoisomers--Synthesis
Bioactive compounds--Synthesis
Pyrrolidines
Persistent Link to This Record: http://purl.flvc.org/FCLA/DT/3331910
Links: http://dx.doi.org/10.1016/0040-4039(95)02267-8
Restrictions on Access: ©1996 Elsevier B.V.
Host Institution: FAU