Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety

Victor O. Rogachev, Victor D. Filimonov, Roland Fröhlich, Olga Kataeva, Peter Metz

The Kizhner Research Center

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

Abstract

A range of novel γ- and enantiopure δ-sultams was prepared by intramolecular [4+2] cycloaddition of vinylsulfonamides with purely thermal activation and under high pressure.

Original language	English
Pages (from-to)	589-595
Number of pages	7
Journal	Heterocycles
Volume	67
Issue number	2
DOIs	https://doi.org/10.3987/COM-05-S(T)80
Publication status	Published - 1 Feb 2006

ASJC Scopus subject areas

Organic Chemistry

Access to Document

10.3987/COM-05-S(T)80

Fingerprint Dive into the research topics of 'Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety'. Together they form a unique fingerprint.

Cite this

Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety. / Rogachev, Victor O.; Filimonov, Victor D.; Fröhlich, Roland; Kataeva, Olga; Metz, Peter.

In: Heterocycles, Vol. 67, No. 2, 01.02.2006, p. 589-595.

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

@article{f87693de25aa4bdaaed3525b14c8408f,

title = "Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety",

abstract = "A range of novel γ- and enantiopure δ-sultams was prepared by intramolecular [4+2] cycloaddition of vinylsulfonamides with purely thermal activation and under high pressure.",

author = "Rogachev, {Victor O.} and Filimonov, {Victor D.} and Roland Fr{\"o}hlich and Olga Kataeva and Peter Metz",

year = "2006",

month = feb,

day = "1",

doi = "10.3987/COM-05-S(T)80",

language = "English",

volume = "67",

pages = "589--595",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "2",

}

TY - JOUR

T1 - Stereoselective synthesis of γ- and δ-sultams by intramolecular diels-alder reaction of vinylsulfonamides possessing an acyclic or carbocyclic 1,3-diene moiety

AU - Rogachev, Victor O.

AU - Filimonov, Victor D.

AU - Fröhlich, Roland

AU - Kataeva, Olga

AU - Metz, Peter

PY - 2006/2/1

Y1 - 2006/2/1

N2 - A range of novel γ- and enantiopure δ-sultams was prepared by intramolecular [4+2] cycloaddition of vinylsulfonamides with purely thermal activation and under high pressure.

AB - A range of novel γ- and enantiopure δ-sultams was prepared by intramolecular [4+2] cycloaddition of vinylsulfonamides with purely thermal activation and under high pressure.

UR - http://www.scopus.com/inward/record.url?scp=33744469407&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33744469407&partnerID=8YFLogxK

U2 - 10.3987/COM-05-S(T)80

DO - 10.3987/COM-05-S(T)80

M3 - Article

AN - SCOPUS:33744469407

VL - 67

SP - 589

EP - 595

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

IS - 2

ER -