111540-02-4Relevant articles and documents
Acid-catalyzed chirality-transferring intramolecular Friedel-Crafts cyclization of α-hydroxy-α-alkenylsilanes
Sakaguchi, Kazuhiko,Kubota, Shunnichi,Akagi, Wataru,Ikeda, Naoko,Higashino, Masato,Ariyoshi, Shoma,Shinada, Tetsuro,Ohfune, Yasufumi,Nishimura, Takahiro
supporting information, p. 8635 - 8638 (2019/07/25)
Acid-catalyzed intramolecular Friedel-Crafts cyclization of optically active α-hydroxy-α-alkenylsilanes possessing a benzene ring (>99% ee) with TMSOTf as a Lewis acid gave enantio-enriched tetrahydronaphthalenes (up to 98% ee). The silyl group attached to the chiral carbon played a crucial role in the chirality transfer.
Dual role of allylsamarium bromide as a Grignard reagent and a single electron transfer reagent in the one-pot synthesis of terminal olefins
Li, Ying,Hu, Yuan-Yuan,Zhang, Song-Lin
supporting information, p. 10635 - 10637 (2013/11/06)
The utility of allylsamarium bromide, both as a nucleophilic reagent and a single-electron transfer reagent, in the reaction of carbonyl compounds with allylsamarium bromide in the presence of diethyl phosphate is reported in this communication. From a synthetic point of view, a simple one-pot method for the preparation of terminal olefins is developed.
The preparation of [pentane-5,5,5-3H3]-abnormal- cannabidiol
Byard, Stephen J.,Carr, Steven A.,DeFaria, Jose F.,Filer, Crist N.,Herbert, John M.,Forcadac, Tatiana Jaramillo
experimental part, p. 180 - 184 (2012/05/20)
A bromoalkane precursor was synthesized in six steps, and its copper catalysed coupling with methylmagnesium chloride to provide unlabelled abnormal-cannabidiol (1a) was optimized. The methodology was used for an analogous coupling using [3Hsu
Intramolecular anodic olefin coupling reactions and the use of electron-rich aryl rings
New, Dallas G.,Tesfai, Zerom,Moeller, Kevin D.
, p. 1578 - 1598 (2007/10/03)
The utility of intramolecular anodic olefin coupling reactions involving electron-rich aromatic rings for constructing fused, bicyclic ring skeletons has been examined. Reactions involving alkoxy-substituted phenyl rings were found to benefit strongly from a 3-methoxy substituent on the phenyl ring. Although overoxidation of the bicyclic product was observed in these reactions, this problem could be minimized with the use of controlled potential electrolysis conditions when a monomethoxy phenyl ring was used and avoided entirely with the use of a vinyl sulfide moiety as the initiator when a more electron-rich phenyl ring was used. Reactions involving 4-alkoxy-substituted phenyl rings as substrates did not lead to good yields of fused products. Furan rings were found to be excellent coupling partners for the reactions and afforded products having fused, bicyclic furan ring skeletons. Cyclizations involving furans were shown to be compatible with the formation of both six- and seven-membered rings, the generation of a quaternary carbon, and the use of a variety of electron-rich olefins as the other coupling partner. It appears that the furan can serve as either the initiating group or the terminating group for the cyclizations. Finally, the reactions were shown to be compatible with the use of a pyrrole ring as one of the participants.
A simple and efficient synthesis of 5'-(2H3)olivetol
Girard, Michel,Moir, David B.,Apsimon, John W.
, p. 189 - 190 (2007/10/02)
The title compound 1 was prepared in 13percent overall yield starting from the commercially available and inexpensive 3,5-dimethoxybenzoic acid (4).The n-pentyl side chain was elaborated from cross-coupling reactions between halides.
