Control elements in the asymmetric tandem alkylation of α-alkylidene-γ-butyrolactone derivatives
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (25) , 3027-3030
- https://doi.org/10.1016/s0040-4039(00)98609-x
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Enantiospecific total synthesis of (-)-megaphone by a highly controlled consecutive 1,4- and 1,3-asymmetric inductionTetrahedron Letters, 1985
- A paradigm for diastereoselectivity in electrophilic attack on trigonal carbon adjacent to a chiral centre: the methylation and protonation of some open–chain enolatesJournal of the Chemical Society, Chemical Communications, 1985
- Diastereoselectivity in the alkylation of enolates having an adjacent silkyl groupJournal of the Chemical Society, Chemical Communications, 1984
- The opposite diastereoselectivity in the alkylation and protonation of enolatesJournal of the Chemical Society, Chemical Communications, 1984
- Staggered models for asymmetric induction: attack trajectories and conformations of allylic bonds from ab initio transition structures of addition reactionsJournal of the American Chemical Society, 1982
- Origin of .pi.-facial stereoselectivity in additions to .pi.-bonds: generality of the anti-periplanar effectJournal of the American Chemical Society, 1981
- Principle of orbital distortionThe Journal of Organic Chemistry, 1981
- Über die Stereoselektivität der α‐Alkylierung von (1R, 2S) (+)‐cis‐2‐hydroxy‐cyclohexancarbonsäureäthylesterHelvetica Chimica Acta, 1980
- Stereocontrol in the synthesis of acyclic systems: applications to natural product synthesisTetrahedron, 1980
- Allylic strain in six-membered ringsChemical Reviews, 1968