A short synthesis of (R)-(+)-frontalin and Latia luciferin using new organosilicon reagents
- 1 January 1978
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 7,p. 297-298
- https://doi.org/10.1039/c39780000297
Abstract
3R-(–)-Linalool and β-dihydroionone have been converted into 3R-(+)-frontalin (3) and Latia luciferin (4), respectively, using α,β-epoxysilanes as the key intermediates.This publication has 2 references indexed in Scilit:
- Synthesis of one enantiomer, the other enantiomer, and a mixture of both enantiomers of frontalin from a derivative of methyl-α-D-glucopyranosideJournal of the Chemical Society, Chemical Communications, 1976
- The structure of Latia luciferinBiochemistry, 1968