125130-61-2Relevant articles and documents
Synthesis of chiral 3-substituted indanones via an enantioselective reductive-heck reaction
Minatti, Ana,Zheng, Xiaolai,Buchwald, Stephen L.
, p. 9253 - 9258 (2008/03/13)
(Chemical Equation Presented) An efficient intramolecular palladium-catalyzed, asymmetric reductive-Heck reaction has been developed, which allowed for the synthesis of either enantiomerically enriched 3-substituted indanones or α-exo-methylene indanones depending on the base used.
Synthesis of 2,3-dihydro-6,7-dimethoxy-2-(3,4-methylenedioxyphenyl)--benzopyran-4-one and its dehydro derivative
Parmar, V. S.,Gupta, Sandhya,Sharma, V. K.,Boll, P. M.
, p. 268 - 269 (2007/10/02)
2,3-Dihydro-6,7-dimethoxy-2-(3,4-methylenedioxyphenyl)--benzopyran-4-one (1), a constituent of Macaranga indica Wight and 6,7-dimethoxy-2-(3,4-methylenedioxyphenyl)--benzopyran-4-one (2) have been synthesized.The spectral characteristics of syntheti