专利号:US-5219845-A 优先权日:1991-04-25 标题:Phosphonates as anti-inflammation agents 发明人:SALARI HASSAN; BITTMAN ROBERT 权利人:UNIV BRITISH COLUMBIA 摘要:The invention pertains to the synthesis and use as therapeutic agents of a group of substances with a glycerol backbone or aliphatic chain structure linked to a phosphorus atom and a polar head group. Depending on the polar head group, the substance has anti-cancer, anti-inflammatory, anti-allergy or anti-cardiovascular disease properties. Compounds of the formula: wherein n is 0 to 14 and R1 is an alkyl group of C12-C20, R2 is a methyl group, and wherein R3 is an inositol analog head group, a (CH2)mN+(CH3)3 group with m=2 to 10, a serine head group, or an ethanolamine head group, or of the formula wherein R1 and R2 are as described above, n=0 or 1, and R3 is (CH2)mN+(CH3)3 (m=2-10) are claimed. This invention also pertains to the synthesis and use as therapeutic agents of a group of substances that have no glycerol backbone but have an aliphatic chain structure linked directly to a phosphorus atom of the general formula R-P(O)(O-)OR' wherein R is a long-chain alkyl group such as hexadecyl or octadecyl and R' is a head group such as choline, glycerol, inositol, ethanolamine, or serine.
专利号:US-5369097-A 优先权日:1991-04-25 标题 :Phosphonates as anti-cancer agents 发明人:SALARI HASSAN; BITTMAN ROBERT 权利人:UNIV BRITISH COLUMBIA 摘要:This invention pertains to the synthesis and use as therapeutic agents of a group of substances with a glycerol backbone or aliphatic chain structure linked to a phosphorus atom and a polar head group. Depending on the polar head group, the substance has anti-cancer, anti-inflammatory, anti-allergy or anti-cardiovascular disease properties. Compounds of the formula: wherein n is 0 to 14 and R1 is an alkyl group of C12-C20, R2 is a methyl group, and wherein R3 is an inositol analog head group, a (CH2)mN+(CH3)3 group with m=2 to 10, a serine head group, or an ethanolamine head group, or of the formula wherein R1 and R2 are as described above, n=0 or 1, and R3 is (CH2)mN+(CH3)3(m=2-10 ) are claimed. This invention also pertains to the synthesis and use as therapeutic agents of a group of substances that have no glycerol backbone but have an aliphatic chain structure linked directly to a phosphorus atom of the general formula R-P(O)(O-)OR' wherein R is a long-chain alkyl group such as hexadecyl or octadecyl and R' is a head group such as choline, glycerol, inositol, ethanolamine, or serine.
参考标题:Total Synthesis Of (−)-21-Isopentenylpaxilline 作者:Amos B. Smith,Haifeng Cui |发布日期:2003.2.1 摘要:[structure: See Text] The Total Synthesis Of (-)-21-Isopentenylpaxilline (1) Has Been Achieved. Key Elements Of The Synthesis Include The Stereocontrolled Construction Of The Advanced Eastern Hemisphere (-)-5, A Highly Efficient Union Of The Eastern And Western Fragments (-)-5 And 4, Respectively, Exploiting Our 2-Substituted Indole Synthesis, And A New Protocol For The Construction Of Ring C.
合成参考文献
摘要:Huang, J.; Ma, D., Science of Synthesis: Special Topics, (2022) 1, 22.