Acid Chloride Of (2S)-α-Ethyl N-Trifluoroacetylaspartate置于吡啶,盐酸体系中,用 乙醚,水,甲苯 用作溶剂,化学反应 9.0H,反应生成L-丝氨酸乙酯盐酸盐 参考文献:Field,Steven J.; Young,Douglas W.,Journal Of The Chemical Society. Perkin Transactions I,1982,P. 591-594 标题:Field,Steven J.; Young,Douglas W.,Journal Of The Chemical Society. Perkin Transactions I,1982,P. 591-594
专利号:US-8461289-B2 优先权日:2006-10-17 标 题:Bioresorbable polymers synthesized from monomer analogs of natural metabolites 发明人:KOHN JOACHIM B; BOLIKAL DURGADAS 权利人:KOHN JOACHIM B; BOLIKAL DURGADAS; UNIV RUTGERS 摘要:New bioresorbable polymers are synthesized from monomer analogs of natural metabolites In particular, polymers are polymerized from analogs of amino acids that contribute advantageous synthesis, processing and material properties to the polymers prepared therefrom, including particularly advantageous degradation profiles.
专利号:US-2772281-A 优先权日:1954-12-23 标题 :Synthesis of 4-amino-3-isoxazolidone and its derivatives 发明人:HOLLY FREDERICK W; STAMMER CHARLES H 权利人:MERCK & CO INC
专利号:US-9744173-B2 优先权日:2014-04-10 标题 :2-amino 6-methyl-4,4a,5,6-tetrahydropyrano[3,4-d][1,3]thiazin-8a(8H)-yl-1,3-thiazol-4-yl amides 发明人:BRODNEY MICHAEL AARON; BECK ELIZABETH MARY; BUTLER CHRISTOPHER RYAN; ZHANG LEI; O'NEILL BRIAN THOMAS; BARREIRO GABRIELA; LACHAPELLE ERIK ALPHIE; ROGERS BRUCE NELSEN 权利人:PFIZER 摘要:The present invention is directed to compounds, tautomers and pharmaceutically acceptable salts of the compounds which are disclosed, wherein the compounds have the structure of Formula I, n nand the variable R 1 is as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
专利号:JP-2001503782-A 优先权日:1996-11-22 标题 :Method and compound for inhibiting release of beta-amyloid peptide and / or its synthesis
专利号:CN-103288916-A 优先权日:2012-02-29 标题:Derivatives, synthesis methods and uses of tanshinone compounds
专利号:CN-1238779-A 优先权日:1996-11-22 标题:Methods and compounds for inhibiting the release of beta-amyloid peptide and/or its synthesis
参考标题:The Total Synthesis Of The Bioactive Natural Product Plantazolicin A And Its Biosynthetic Precursor Plantazolicin B 作者:Sabine Fenner,Zoe E. Wilson,Steven V. Ley |发布日期:2016.10.24 摘要:Herein, We Describe Our Full Investigations Into The Synthesis Of The Peptide‐derived Natural Product Plantazolicin A, A Compound That Demonstrates Promising Selective Activity Against The Causative Agent Of Anthrax Toxicity, And Its Biosynthetic Precursor Plantazolicin B. This Report Particularly Focuses On The Challenging Preparation Of The Arginine Containing Thiazole Fragment, Including The Development
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参考文献:10.1007/s00270-024-03747-4 摘要:Soga Y, Iida O, Seki S, Kawasaki D, Anzai H, Ando H, Nakama T, Shinozaki N, Kozuki A, Ishihara M, Urasawa K, Toi S, Tsujita H, Tobita K, Ogata K, Horie K, Hayakawa N, Mori S, Fujihara M, Ohki T, Yuba K, Mano T, Ando K, Nakamura M, , Ikari Y, Shinke T, Saito S, Shibata Y, Kishi K. Twenty-Four-Month Safety and Effectiveness of TCD-17187 Drug-Coated Balloon for Treatment of Atherosclerotic Lesions in Superficial Femoral and Proximal Popliteal Artery. Cardiovasc Intervent Radiol. 2024 May 30;47(6):730–40. doi: 10.1007/s00270-024-03747-4.