Le dimethyl acetal du diazoacetaldehyde: une nouvelle voie d'acces aux cyclopropanes aldehydes et aux formyl pyrazoles.
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (23) , 2239-2242
- https://doi.org/10.1016/0040-4039(80)80013-x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Total stereospecific synthesis of -chrysanthemic methyl ester : the cyclopropenic way.Tetrahedron Letters, 1980
- Alkaloids from nitronesAccounts of Chemical Research, 1979
- Electrophilic cyclopropanes in organic synthesisAccounts of Chemical Research, 1979
- Use of intramolecular [3 + 2] cycloaddition reactions in the synthesis of natural products. A stereospecific synthesis of (.+-.)-biotin from cyclohepteneJournal of the American Chemical Society, 1978
- Cycloadditions of diazoesters to α,β-unsaturated aldehydesTetrahedron, 1978
- Synthesis of α-diazoaldehydesCollection of Czechoslovak Chemical Communications, 1970
- Reaktionen der β‐Alkoxyalkyl‐carbeneEuropean Journal of Inorganic Chemistry, 1967