Cycloheptadiene ring synthesis by tandem intermolecular enyne metathesis.Org Lett. 2003 Sep 18; 5(19):3463-6.OL
Abstract
[reaction: see text] The tandem intermolecular enyne metathesis between 1-alkynes and cyclopentene is reported, providing 2-substituted 1,3-cycloheptadienes. The success of the intermolecular reaction hinges on an appropriate balance between cycloalkene ring strain and reactivity of the alkyne.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Language
eng
PubMed ID
12967300
Citation
Kulkarni, Amol A., and Steven T. Diver. "Cycloheptadiene Ring Synthesis By Tandem Intermolecular Enyne Metathesis." Organic Letters, vol. 5, no. 19, 2003, pp. 3463-6.
Kulkarni AA, Diver ST. Cycloheptadiene ring synthesis by tandem intermolecular enyne metathesis. Org Lett. 2003;5(19):3463-6.
Kulkarni, A. A., & Diver, S. T. (2003). Cycloheptadiene ring synthesis by tandem intermolecular enyne metathesis. Organic Letters, 5(19), 3463-6.
Kulkarni AA, Diver ST. Cycloheptadiene Ring Synthesis By Tandem Intermolecular Enyne Metathesis. Org Lett. 2003 Sep 18;5(19):3463-6. PubMed PMID: 12967300.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Cycloheptadiene ring synthesis by tandem intermolecular enyne metathesis.
AU - Kulkarni,Amol A,
AU - Diver,Steven T,
PY - 2003/9/12/pubmed
PY - 2004/2/10/medline
PY - 2003/9/12/entrez
SP - 3463
EP - 6
JF - Organic letters
JO - Org Lett
VL - 5
IS - 19
N2 - [reaction: see text] The tandem intermolecular enyne metathesis between 1-alkynes and cyclopentene is reported, providing 2-substituted 1,3-cycloheptadienes. The success of the intermolecular reaction hinges on an appropriate balance between cycloalkene ring strain and reactivity of the alkyne.
SN - 1523-7060
UR - https://www.unboundmedicine.com/medline/citation/12967300/Cycloheptadiene_ring_synthesis_by_tandem_intermolecular_enyne_metathesis_
DB - PRIME
DP - Unbound Medicine
ER -