ABSOLUTE CONFIGURATIONS OF (+)-METHYL TODOMATUATE AND ITS NEW ANALOGUES, PSEUDOTSUGONAL AND AR-PSEUDOTSUGONAL, ISOLATED FROM DOUGLAS-FIR WOOD
- 5 May 1973
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 2 (5) , 491-494
- https://doi.org/10.1246/cl.1973.491
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Juvenile Hormone Mimics in Conifers. I. Isolation of (−)-cis-4-[1′(R)-5′-Dimethyl-3′-oxohexyl]-cyclohexane-1-carboxylic Acid from Douglas-fir WoodCanadian Journal of Chemistry, 1972
- Syntheses of Natural(+)-Juvabione, Its Enantiomer(-)-Juvabione, and Their Diastereoisomers (+)- and (-)-EpijuvabioneJournal of the American Chemical Society, 1970
- The Structure and Stereochemistry of Four New Sesquiterpenes Isolated from the Wood Oil of “Kaya” (Torreya nucifera)Bulletin of the Chemical Society of Japan, 1965
- Terpenoids—LXIXTetrahedron, 1965
- Terpenoids—LXTetrahedron, 1964
- 4-(p-Tolyl)-1-pentanol in Douglas Fir Pulping Products1The Journal of Organic Chemistry, 1963