(Z)-7-Nitro-3-Heptene as Central Intermediate for the Synthesis of Jasmone, Methyl Jasmonate, and γ Jasmolactone
- 1 February 1989
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 19 (3-4) , 575-583
- https://doi.org/10.1080/00397918908050702
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Amberlyst-A21 as a New and Efficient Surface Catalyst for the Conjugate Addition of Nitroalkanes to Methyl Acrylate: An Improved Synthesis of Methyl 4-Nitro- and 4-Oxo-alkanoatesSynthesis, 1987
- Conjugate Addition of Nitro-Derivatives to α,β-Unsaturated Carbonyl Compounds on Basic AluminaSynthesis, 1986
- A Facile Displacement of Tertiary Nitro Group by Hydrogen with Sodium HydrogentellurideBulletin of the Chemical Society of Japan, 1985
- Denitrohydrogenation of aliphatic nitro compounds and a new use of aliphatic nitro compounds as radical precursorsTetrahedron, 1985
- Synthesis of 2-Nitroalkanols on Alumina Surfaces without Solvent: A Simple, Mild and Convenient MethodSynthesis, 1983
- Denitration of α-Nitroketones by Treatment of their Tosylhydrazones with Lithium Aluminium Hydride; New Applications of the Henry ReactionSynthesis, 1983
- Reductive displacement of the nitro group into hydrogen in primary α-nitroketonesTetrahedron Letters, 1982
- Synthesis of Three Jasmin Constituents via a Central IntermediateHelvetica Chimica Acta, 1978
- N,N-diethylaminoacetonitrile a generally useful latent acyl carbanionTetrahedron Letters, 1978
- Synthesis of Jasmonoids, a ReviewSynthetic Communications, 1974