Synthesis of enantiomerically pure (10,11)-(+)-juvenile hormones I and II
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 44 (2) , 343-354
- https://doi.org/10.1016/s0040-4020(01)85826-9
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Alkylation of enolates from .beta.-dicarbonyl compounds with sulfonium salt electrophilesThe Journal of Organic Chemistry, 1983
- THE STEREOSELECTIVE SYNTHESIS OF C18-JUVENILE HORMONE ANALOGUEChemistry Letters, 1975
- THE STEREOSPECIFIC PREPARATION OF METHYL FARNESOATE AND SYNTHETIC PRECURSORS OF C18- AND C17 JUVENILE HORMONESChemistry Letters, 1974
- THE HIGHLY STEREOSELECTIVE SYNTHESIS OF ETHYL GERANATEChemistry Letters, 1974
- Conversion of Farnesol into Methyl dl-12-Homo-10-trans-juvenate. the 10-trans-Isomer of dl-C17-Cecropia Juvenile HormoneAgricultural and Biological Chemistry, 1972
- A Synthesis of dl-C17-Cecropia Juvenile HormoneAgricultural and Biological Chemistry, 1972
- Synthesis of C-18 Cecropia juvenile hormone to obtain optically active forms of known absolute configurationJournal of the American Chemical Society, 1971
- Absolute configuration of the C18 juvenile hormone: application of a new circular dichroism method using tris(dipivaloylmethanato)praseodymiumJournal of the Chemical Society D: Chemical Communications, 1971
- The optical activity of the Cecropia juvenile hormonesBiochemical and Biophysical Research Communications, 1970
- Juvenile hormone of Hyalophora cecropiaAccounts of Chemical Research, 1970