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 | |
| Publication status | Published - 1 Feb 2006 |
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ASJC Scopus subject areas
- Organic Chemistry
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
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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 -