157360-23-1Relevant articles and documents
A new strategy for the synthesis of 4,6-di-tert-butyl-2,2-dipentyl-2,3- dihydro-5-benzofuranol (BO-653), a potent antiatherogenic antioxidant
Murakata, Masatoshi,Kimura, Masahiro
scheme or table, p. 4950 - 4952 (2011/01/04)
An efficient alternative route to 4,6-di-tert-butyl-2,2-dipentyl-2,3- dihydro-5-benzofuranol (BO-653), a potent antiatherogenic antioxidant, has been developed by the application of the base-promoted dienone- phenol rearrangement reaction. A decisive effect of MgBr2 in the reaction of Grignard reagents is also described.
Process for preparation of a benzofuran derivative
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Page/Page column 15, (2010/01/31)
An industrially useful process for producing benzofuran derivatives of formula (1) by formylating a compound of formula (2) (where A1 is a protective group), followed by reaction with a compound of formula (4) (where X1 is a halogen atom), then performing a cyclizing reaction and subsequently performing a reaction for hydroxyl group deprotection.
Prophylactic/therapeutic agents for atherosclerosis
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, (2008/06/13)
PCT No. PCT/JP98/01861 Sec. 371 Date Nov. 8, 1999 Sec. 102(e) Date Nov. 8, 1999 PCT Filed Apr. 23, 1998 PCT Pub. No. WO98/50025 PCT Pub. Date Nov. 12, 1998Herein disclosed are prophylactic/therapeutic agents for atherosclerosis containing a compound of general formula (1): wherein R1 represents a hydrogen atom or an acyl group, R2 represents a lower alkyl group, R3 represents a hydrogen atom or a lower alkyl group, and R4, R5 and R6 represent a hydrogen atom, an alkyl group, an alkenyl group, an alkynyl group or an aryl group, or R2 and R4 together with the oxygen atom may form a furan or dihydrofuran ring, or R5 and R6 may combine to form a cycloalkyl group or a heterosubstituted cycloalkyl group in which one or more methylene groups of the cycloalkyl group are replaced by oxygen, sulfur or alkyl-substituted nitrogen atoms, a possible optically active isomer or a pharmaceutically acceptable salt thereof, as an active ingredient.