The concerted mechanism of acylamidation. Syn-stereospecificity of the reaction.

Ilya D. Gridnev; Aleksey V. Shastin; Elisabeth S. Balenkova

doi:10.1016/S0040-4020(01)80989-3

The concerted mechanism of acylamidation. Syn-stereospecificity of the reaction.

Ilya D. Gridnev, Aleksey V. Shastin, Elisabeth S. Balenkova

Research output: Contribution to journal › Article › peer-review

15 Citations (Scopus)

Abstract

The concerted mechanism for the new reaction of acylamidation of alkenes and alkynes is proposed on the basis of syn-stereospecifity observed and the study of the reagent structure.

Original language	English
Pages (from-to)	5577-5584
Number of pages	8
Journal	Tetrahedron
Volume	47
Issue number	29
DOIs	https://doi.org/10.1016/S0040-4020(01)80989-3
Publication status	Published - 1991 Jul 15
Externally published	Yes

Keywords

6-fluoro-5,6-dihydro-1,3-oxazines
acylamidation
acylation
cycloaddition.
β-amidoketones

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4020(01)80989-3

Cite this

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title = "The concerted mechanism of acylamidation. Syn-stereospecificity of the reaction.",

abstract = "The concerted mechanism for the new reaction of acylamidation of alkenes and alkynes is proposed on the basis of syn-stereospecifity observed and the study of the reagent structure.",

keywords = "6-fluoro-5,6-dihydro-1,3-oxazines, acylamidation, acylation, cycloaddition., β-amidoketones",

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AU - Gridnev, Ilya D.

AU - Shastin, Aleksey V.

AU - Balenkova, Elisabeth S.

PY - 1991/7/15

Y1 - 1991/7/15

N2 - The concerted mechanism for the new reaction of acylamidation of alkenes and alkynes is proposed on the basis of syn-stereospecifity observed and the study of the reagent structure.

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KW - 6-fluoro-5,6-dihydro-1,3-oxazines

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KW - acylation

KW - cycloaddition.

KW - β-amidoketones

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The concerted mechanism of acylamidation. Syn-stereospecificity of the reaction.

Abstract

Keywords

ASJC Scopus subject areas

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