SYNTHESIS OF CAMPHOR-DERIVED CHIRAL CYCLOPENTADIENES VIA THE NAZAROV CYCLIZATION - PREPARATION OF CHIRAL BIS(CYCLOPENTADIENYL)ZIRCONIUM ANDBIS(CYCLOPENTADIENYL)TITANIUM DICHLORIDES

Citation
Rl. Halterman et A. Tretyakov, SYNTHESIS OF CAMPHOR-DERIVED CHIRAL CYCLOPENTADIENES VIA THE NAZAROV CYCLIZATION - PREPARATION OF CHIRAL BIS(CYCLOPENTADIENYL)ZIRCONIUM ANDBIS(CYCLOPENTADIENYL)TITANIUM DICHLORIDES, Tetrahedron, 51(15), 1995, pp. 4371-4382
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404020
Volume
51
Issue
15
Year of publication
1995
Pages
4371 - 4382
Database
ISI
SICI code
0040-4020(1995)51:15<4371:SOCCCV>2.0.ZU;2-0
Abstract
Nazarov cationic pi-cyclizations were employed in the synthesis of thr ee substituted camphor-derived cyclopentadienyl ligands bearing a 3-me thyl, 3-t-butyl or 3-phenyl substituent on the 0,10-trimethyltricyclo[ 5,2,1,0(2,6)]deca-2,5-diene framework. These ligands were converted to diastereomeric mixtures of bis(cyclopentadienyl)zirconium and -titani um dichlorides. In each case a C-2-symmetrical isomer was the major is omer in the crude reaction product mixture and in all but one case a p ure C-2-symmetrical diastereomer could be obtained by recrystallizatio n.