3917-39-3Relevant articles and documents
INCORPORATION OF α-IONYLIDENE ETHANOL AND α-IONYLIDENE ACETIC ACID INTO ABSCISIC ACID BY CERCOSPORA ROSICOLA
Neill, Steven J.,Horgan, Roger
, p. 2469 - 2472 (1983)
2H-Labelled α-ionylidene ethanol and α-ionylidene acetic acid are converted in high yield to 1'-deoxy-abscisic acid (1'-deoxy-ABA) and abscisic acid (ABA) by Cercospora rosicola.Incorporation of label was confirmed by mass spectrometry.The 2-trans isomers
Agents for use on skin and/or hair containing quadruply substituted cyclohexene compounds
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Page/Page column 12-13, (2010/11/28)
The invention relates to agents for use on skin or hair, particularly for increasing skin tanning and the synthesis of melanin in skin or hair. The invention contains, in particular, cosmetic or dermatological preparations containing quadruply substituted
Palladium-catalyzed coupling reaction of an enol nonaflate with (vinyl)tributylstannanes and acetylenes: A highly stereoselective synthesis of 8,18-13C2-labeled retinal
Wada, Akimori,Ieki, Yasuhiro,Nakamura, Saeko,Ito, Masayoshi
, p. 1581 - 1588 (2007/10/03)
Here we report that enol nonaflates exhibit higher reactivity than the corresponding enol triflates in palladium-catalyzed cross-coupling reactions with various (vinyl)tributylstannanes and acetylenes. We also highlight the reaction of a vinyl nonaflate,