A New Route to the Enantioselective Synthesis of Cycloheptenols. Temperature Effects in the Asymmetric Reductive Ring Opening of [3.2.1] Oxabicycloalkenes
- 1 November 1997
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (45) , 11090-11091
- https://doi.org/10.1021/ja971770m
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- General Strategy toward the Tetrahydronaphthalene Skeleton. An Expedient Total Synthesis of SertralineThe Journal of Organic Chemistry, 1997
- Using ring-opening reactions of oxabicyclic compounds as a strategy in organic synthesisPublished by Springer Nature ,1997
- Nonlinear Temperature Behavior of Product Ratios in Selection ProcessesAngewandte Chemie International Edition in English, 1996
- Asymmetric synthesis of the lactone moiety of mevinic acidTetrahedron Letters, 1995
- Nickel-Catalyzed Hydroalumination of Oxabicyclic Alkenes. Ligand Effects on the Regio- and EnantioselectivityJournal of the American Chemical Society, 1995
- Asymmetric grignard addition to aldéhydes. An example of inverse temperature dependence of enantiomeric excess.Tetrahedron: Asymmetry, 1994
- Temperature Effects in Asymmetric Dihydroxylation: Evidence for a Stepwise MechanismAngewandte Chemie International Edition in English, 1993
- The Isoinversion Principle—a General Model of Chemical SelectivityAngewandte Chemie International Edition in English, 1991
- Use of alkaloids and aminoalcohols in catalytic asymmetric induction:Temperature effect on the addition of diethylzinc to benzaldehydeTetrahedron Letters, 1987
- Reduction asymetrique de cetones par des alcoxyaluminohydrures chiraux prepares a partir de l'ephedrine et divers alcools ou phenols achirauxTetrahedron, 1976