Baker's yeast reduction of prochiral γ-nitroketones. II.1 straightforward enantioselective synthesis of 2,7-dimethyl-1,6-dioxaspiro[4.4]nonanes
- 1 December 1995
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (12) , 2971-2976
- https://doi.org/10.1016/0957-4166(95)00394-0
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Baker's yeast reduction of prochiral γ-nitroketones: Enantioselective synthesis of (S)-4-nitroalcoholsTetrahedron, 1995
- A simple, efficient, two‐step synthesis of symmetric 2,7‐dialkyl‐1,6‐dioxaspiro[4.4]nonanesJournal of Heterocyclic Chemistry, 1994
- Enantioselective synthesis of indolizine derivatives by rearrangement-cyclization of isoxazoline-5-spirocyclopropanesTetrahedron, 1993
- Asymmetric synthesis of a pheromone for Andrena haemorrhoa F from a chiral nitro alcohol obtained by the yeast reduction of a nitro ketoneTetrahedron, 1990
- Synthesis of Spiroacetal Pheromones via Metalated HydrazonesSynthesis, 1990
- Chemistry of fruit flies: composition of the male rectal gland secretions of some species of South-East Asian Dacinae. Re-examination of Dacus cucurbitae(melon fly)Journal of the Chemical Society, Perkin Transactions 1, 1990
- Multicomponent Mandibular Gland Secretions in Three Species of Andrena Bees (Hym., Apoidea)Zeitschrift für Naturforschung C, 1982
- Pheromone Bouquet of the Mandibular Glands in Andrena haemorrhoa F. (Hym., Apoidea)Zeitschrift für Naturforschung C, 1981
- Spiroketals in the mandibular glands ofAndrena beesThe Science of Nature, 1980
- Specification of the stereospecificity of some oxido-reductases by diamond lattice sectionsPure and Applied Chemistry, 1964