Optically active cyclopropanols by samarium(II) iodide induced intramolecular reductive cyclisation of β-chlorosubstituted amides

DOI: 10.1016/0957-4166(94)80010-3

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Tetrahedron Asymmetry p. 531 - 534 (1994)

Update date:2022-08-03

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Fadel

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Article abstract of DOI:10.1016/0957-4166(94)80010-3

Samarium diiodide promotes under mild conditions, intramolecular reductive cyclisation of β-chloro substituted amides, and leads with an excellent diastereomeric excess and high yield to functionalised optically active cyclopropranols.

Full text of DOI:10.1016/0957-4166(94)80010-3

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Optically active cyclopropanols by samarium(II) iodide induced intramolecular reductive cyclisation of β-chlorosubstituted amides

DOI: 10.1016/0957-4166(94)80010-3

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0957-4166(94)80010-3

Full text of DOI:10.1016/0957-4166(94)80010-3

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