A NOVEL METHOD OF CYCLIZATION BY MEANS OF ALKENE METATHESIS - A SYNTHETIC STRATEGY OF CARBOCYCLIC-COMPOUNDS AND HETEROCYCLIC-COMPOUNDS

Authors
Citation
J. Tsuji, A NOVEL METHOD OF CYCLIZATION BY MEANS OF ALKENE METATHESIS - A SYNTHETIC STRATEGY OF CARBOCYCLIC-COMPOUNDS AND HETEROCYCLIC-COMPOUNDS, Yuki Gosei Kagaku Kyokaishi, 55(12), 1997, pp. 1101-1113
Citations number
78
Journal title
ISSN journal
00379980
Volume
55
Issue
12
Year of publication
1997
Pages
1101 - 1113
Database
ISI
SICI code
0037-9980(1997)55:12<1101:ANMOCB>2.0.ZU;2-4
Abstract
Historical background of alkene metathesis is briefly reviewed. The in troduction of the Schrock Mo carbene complex and the Grubbs Ru-carbene complexes has initiated rapid development of synthetic utility of alk ene metathesis. Many functional groups are tolerated without protectio n in the Mo and Ru catalysed metathesis. Among several synthetic appli cations of the alkene metathesis, the ring closing metathesis offers a n extremely useful method for cyclization to give carbo- and hetero-cy clic compounds from medium to large sizes. A number of naturally occur ring macrocyclic compounds have been synthesized in shorter steps by t he ring closing metathesis using the Ru complex as key reaction. The a lkene metathesis has brought in a dramatic change in synthetic designs of complex cyclic compounds.