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  Stereoselective Synthesis of Highly Functionalized γ-Lactones via Iodolactonization

Reetz, M. T., & Lauterbach, E. H. (1993). Stereoselective Synthesis of Highly Functionalized γ-Lactones via Iodolactonization. Heterocycles, 35(2), 627-630. doi:10.3987/COM-92-S(T)94.

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 Creators:
Reetz, Manfred T.1, Author              
Lauterbach, Erik H., Author
Affiliations:
1Research Department Reetz, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445588              

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 Abstract: Chiral γ-amino α,β-unsaturated carboxylic acids (5) derived from L-amino acids undergo diastereofacially selective iodolactonization with formation of the highly functionalized lactones (7)

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Language(s): eng - English
 Dates: 1993
 Publication Status: Published in print
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.3987/COM-92-S(T)94
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Title: Heterocycles
Source Genre: Journal
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Publ. Info: Sendai, Japan : Elsevier
Pages: - Volume / Issue: 35 (2) Sequence Number: - Start / End Page: 627 - 630 Identifier: ISSN: 0385-5414
CoNE: https://pure.mpg.de/cone/journals/resource/954925528872