📜豆甾醇置于氧气,环己酮,Aluminum Isopropoxide,臭氧体系中,用 二氯甲烷,甲苯 作为反应溶剂,化学反应 1.13H,反应生成 二去甲胆烯醛 参考文献:Structure And Synthesis Of A Progesterone Homologue From The Skin Of The Dorid Nudibranchaldisa Smaragdina 标题:Structure And Synthesis Of A Progesterone Homologue From The Skin Of The Dorid Nudibranchaldisa Smaragdina 摘要: DOI:10.1002/1099-0690(200205)2002:9<1500::Aid-Ejoc1500>3.0.Co;2-D
专利号:US-11479577-B2 优先权日:2016-05-18 标题:Intermediates for the synthesis of bile acid derivatives, in particular of obeticholic acid 发明人:WEYMOUTH-WILSON ALEXANDER; KOMSTA ZOFIA; WALLIS LAURA; EVANS TIMOTHY; DAVIES IEUAN; OTTER CARL; BATCHELOR RHYS 权利人:NZP UK LTD 摘要:The present invention relates to compounds which are intermediates in the synthesis of bile acid derivatives with pharmacological activity. The invention relates to compounds of general formula (I):wherein:, R1, R2, R3, R4, R5, R6 and Y are as defined herein.The compounds are intermediates in the synthesis of synthetic bile acids which are useful in the treatment of conditions such as liver disease. In addition, the invention relates to a method of synthesizing these intermediates and a method of preparing obeticholic acid and obeticholic acid analogues from the compounds of the invention.
专利号:US-10766921-B2 优先权日:2016-05-18 标 题 :Process and intermediates for the 6,7-alpha-epoxidation of steroid 4,6-dienes 发明人:WEYMOUTH-WILSON ALEXANDER; KOMSTA ZOFIA; WALLIS LAURA; EVANS TIMOTHY 权利人:NZP UK LTD 摘要:The invention relates to a process for preparing a compound of general formula (Ia): wherein R2, Y, R4 and R5 are as defined herein, wherein the epoxidation is conducted using an oxidant and methyltrioxorhenium as a catalyst (MeReO3). The invention also relates to certain compounds per se. The compounds are intermediates in the synthesis of synthetic bile acids.
专利号:US-6133280-A 优先权日:1997-02-05 标题 :Androgen synthesis inhibitors 发明人:BRODIE ANGELA; LING YANGZHI 权利人:UNIV MARYLAND 摘要:This invention relates to novel inhibitors of androgen synthesis that are useful in the treatment of prostate cancer and benign prostatic hypertrophy. The present invention also provides methods of synthesizing these novel compounds, pharmaceutical compositions containing these novel compounds, and methods of treating prostate cancer and benign prostatic hypertrophy using the androgen synthesis inhibitors of the present invention.
专利号:US-2019284227-A1 优先权日:2016-05-18 标题:Intermediates for the Synthesis of Bile Acid Derivatives, in Particular of Obeticholic Acid
专利号:WO-2017199033-A1 优先权日:2016-05-18 标题:Intermediates for the synthesis of bile acid derivatives, in particular of obeticholic acid
专利号:US-10968250-B2 优先权日:2016-05-18 标 题:Intermediates for the synthesis of bile acid derivatives, in particular of obeticholic acid