专利号:US-5446158-A 优先权日:1989-01-11 标题:Process for synthesis of FK-506 and tricarbonyl intermediates 发明人:JONES TODD K; MILLS SANDER G; ASKIN DAVID; REAMER ROBERT A; DESMOND RICHARD; TSCHAEN DAVID M; VOLANTE RALPH P; SHINKAI ICHIRO 权利人:MERCK & CO INC 摘要:A process is described for the total synthesis of the macrolide immunosuppressant, FK-506, and important tricarbonyl process intermediates thereof. The tricarbonyl intermediates can be produced by the mild oxidation of 2,3-dihydroxy carboxylate compounds containing olefin moieties.
专利号:US-4594432-A 优先权日:1983-01-28 标题 :Process for the synthesis of 1α,23(S),25-trihydroxycholecalciferol and 1α,23(R),25-trihydroxycholecalciferol 发明人:BAGGIOLINI ENRICO G; USKOKOVIC MILAN R; WOVKULICH PETER M 权利人:HOFFMANN LA ROCHE 摘要:The invention is directed to a process and intermediates for the preparation of 1α,23(S),25-trihydroxycholecalciferol and 1α,23(R),25-trihydroxycholecalciferol. The end-products, 1α,23(S),25-trihydroxycholecalciferol and 1α,23(R),25-trihydroxycholecalciferol, are useful for the treatment of disease states which are characterized by insufficient amounts of 1,25 dihydroxycholecalciferol.
专利号:US-4595776-A 优先权日:1983-03-21 标 题:Synthesis of 1α,25-dihydroxyergocalciferol 发明人:BAGGIOLINI ENRICO G; BATCHO ANDREW D; BORIS ALFRED; USKOKOVIC MILAN R 权利人:HOFFMANN LA ROCHE 摘要:The invention is directed to a process and intermediates for the preparation of 1 alpha ,25-dihydroxyergocalciferol as well as substantially pure and crystalline 1 alpha ,25-dihydroxyergocolciferol. The end-product 1 alpha ,25-dihydroxyergocalciferol is useful in the treatment of disease states which are characterized by insufficient amounts of 1 alpha , 25-dihydroxycholecalciferol.
专利号:US-11827660-B2 优先权日:2019-02-01 标题 :Synthesis strategy for gap protecting group 发明人:SEIFERT COLE 权利人:SEDERMA SA 摘要:The present invention relates to a novel synthesis method to form particular molecules. These molecules have multiple uses, most notably in the field of protecting groups used throughout organic and synthetic chemistry. The disclosed method is safer, more cost- and time-effective, and more amenable to large scale production than those currently known in the art. The protecting groups synthesized are useful in GAP peptide synthesis.
专利号:WO-2010074764-A1 优先权日:2008-12-23 标题 :Synthesis of oligomeric neolignans and their use 发明人:SNYDER SCOTT A; KONTES FERENC 权利人:UNIV COLUMBIA; SNYDER SCOTT A; KONTES FERENC 摘要:Compounds having the structure formule (I) and their uses are described herein.
专利号:KR-0160937-B1 优先权日:1991-05-28 标 题:New Synthesis of 19-Nor Vitamin D Compounds
参考标题:Diphenylphosphinoyl-Mediated Synthesis Of Ketones 作者:David J. Fox,Daniel Sejer Pedersen,Stuart Warren 摘要:α-Diphenylphosphinoyl Ketones Are Selectively And Sequentially Alkylated At The α-Position. Double Lithiation And Selective Alkylation Occurs At The Less Stabilised γ-Position. Dephosphinoylation Of The Alkylation Products Gives Ketones. Mono-Alkylation Is Selective, Highly Crystalline Intermediates Are Formed And A One-Pot Strategy Is Possible. The Method Is Ideally Suited For The Preparation Of Acid-Sensitive Ketones.
合成参考文献
摘要:Schobert, R.; Hölzel, C.; Barnickel, B., Science of Synthesis, (2010) 47, 50. 摘要:Schobert, R.; Hölzel, C.; Barnickel, B., Science of Synthesis, (2010) 47, 46. 摘要:Demchuk, O. M.; Stankevič, M.; Pietrusiewicz, K. M., Science of Synthesis Knowledge Updates, (2015) 1, 321.