Highly enantioselective cyclization using cationic Rh(I) with chiral ligand
- 13 October 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (42) , 6331-6334
- https://doi.org/10.1016/s0040-4039(00)60966-8
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Asymmetric cyclization reactions. Cyclization of substituted 4-pentenals into cyclopentanone derivatives by rhodium(I) with chiral ligandsTetrahedron, 1991
- RhI-catalysed formation of two conformational diastereoisomers due to a cis-cyclohexane-1,2-diol moiety. X-Ray molecular structure of two stereoisomers of 4′-isopropenyl-7,9-dioxabicyclo[4.3.0]nonane-8-spirocyclohexan-3′-yl p-bromobenzoateJournal of the Chemical Society, Perkin Transactions 1, 1991
- Enantioselective conjugate addition of rationally designed chiral cuprate reagents to 2-cycloalkenonesJournal of the American Chemical Society, 1986
- Asymmetric synthesis using enantiomerically pure 2-(p-anisylsulfinyl)-2-cycloalkenonesTetrahedron, 1984
- 2, 2'-bis(diphenylphosphino)-1, 1'-binaphthyl(binap)Tetrahedron, 1984
- Synthesis of 11-Methyl- and 11,11-Dimethylprostaglandins via the Wittig Reaction of α-DienolBulletin of the Chemical Society of Japan, 1978