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

Access to Document

10.1016/S0040-4020(01)80989-3

Fingerprint Dive into the research topics of 'The concerted mechanism of acylamidation. Syn-stereospecificity of the reaction.'. Together they form a unique fingerprint.

Cite this

@article{2f37d488e32745349e29a5b9bcc2fea5,

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",

author = "Gridnev, {Ilya D.} and Shastin, {Aleksey V.} and Balenkova, {Elisabeth S.}",

year = "1991",

month = jul,

day = "15",

doi = "10.1016/S0040-4020(01)80989-3",

language = "English",

volume = "47",

pages = "5577--5584",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier Limited",

number = "29",

}

TY - JOUR

T1 - The concerted mechanism of acylamidation. Syn-stereospecificity of the reaction.

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.

AB - 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.

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

KW - acylamidation

KW - acylation

KW - cycloaddition.

KW - β-amidoketones

UR - http://www.scopus.com/inward/record.url?scp=0025776935&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0025776935&partnerID=8YFLogxK

U2 - 10.1016/S0040-4020(01)80989-3

DO - 10.1016/S0040-4020(01)80989-3

M3 - Article

AN - SCOPUS:0025776935

VL - 47

SP - 5577

EP - 5584

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 29

ER -

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

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this