Alternation of stereocontrol mode in the cyclization of 2-(3′-4′-dimethyl-6′-trimethylsilyl-4′-hexenyl)-2-cyclohexenones by the auxiliary controlling substituents at 1′- and 2′-positions of the side chain
- 1 October 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (44) , 8247-8250
- https://doi.org/10.1016/0040-4039(94)88294-0
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Clerodane diterpenoidsNatural Product Reports, 1992
- Synthetic applications of gilman reagents derived from 2-bromo-2-cycloalken-1-one Ethylene KetalsTetrahedron Letters, 1991
- Folding strain control for remote stereocontrol: diastereoselectivity in the ring closure reactions of 2-(6′-trimethylsilylhex-4′-enyl)cyclohex-2-enones with alkyl groups at various positions in the side chainJournal of the Chemical Society, Chemical Communications, 1989
- One-pot stereospecific construction of cis-clerodane skeleton by means of doubly stereocontrolled cyclization: Total synthesis of linaridialTetrahedron Letters, 1987
- Remarkable stereocontrol observed in the ring formation by intramolecular hosomi-sakurai reactionTetrahedron Letters, 1984