63589-61-7 = 55739-58-7 + 97858-62-3 [标题:Reaction Conditions 标题:Comparative Hplc Enantioseparation Of Thirty-Six Aromatic Compounds On Four Columns Of The Lux Series: Impact Of Substituents,Shapes And Electronic Properties 作者:Peluso,Paola; Et Al 参考文献:Chirality 日期:2013 卷标:25(11) 页码:709-718]
专利号:US-4727146-A 优先权日:1980-07-03 标题 :Synthesis of chiral 1-benzyl-1,2,3,4-tetra-hydroisoquinolines by asymmetric reduction 发明人:RICE KENNER C 权利人:US HEALTH 摘要:In a short total synthesis of morphinan compounds, derivatives of 1-benzyl-1,2,3,4-tetrahydroisoquinoline are produced. Certain of these compounds, although highly aromatic and functionalized, can be optically resolved. The optically active enantiomers can serve as important intermediates for both natural and unnatural opioids. As a special function of this invention, certain of the derivatives, namely 4'-6' and 7'-9', may be hydrogenated to 1'-3' derivative by asymmetric reduction either of the catalytic or chemical type.
专利号:US-12378196-B2 优先权日:2018-12-11 标 题 :Synthesis of (S)-6-hydroxytryptophan and derivatives thereof 发明人:SIMON WERNER; WERNER-SIMON SUSANNE; MüLLER CHRISTOPH 权利人:HEIDELBERG PHARMA RES GMBH 摘要:The present invention relates to novel methods and compounds for synthesizing amanitin derivatives. The invention in particular relates to methods for synthesizing (S)-6-hydroxy-tryptophan derivatives which can be used as building blocks for synthesizing amanitin derivatives or amatoxin drug conjugates. The invention further relates to intermediate compounds of said synthesis pathways for use in amanitin derivative and amatoxin drug conjugate synthesis, and to the use of particular catalysts suited for mediating said synthesis pathways.
专利号:US-8729306-B2 优先权日:2010-02-05 标 题:Process for the preparation of nitrogen substituted aminotetralins derivatives 发明人:VASSELIN DAVID; CARLY NICOLAS; ATES CELAL 权利人:VASSELIN DAVID; CARLY NICOLAS; ATES CELAL; UCB PHARMA GMBH 摘要:The present invention provides an alternative synthesis of N-substituted aminotetralines which synthesis comprises catalytic asymmetric hydrogenation of compounds of general formula (A).
专利号:WO-2010048138-A1 优先权日:2008-10-21 标 题 :Synthesis of intermediates useful for the production of certain cgrp inhibitors and intermediates used in such synthesis 发明人:HADDAD NIZAR; KRISHNAMURTHY DHILEEPKUMAR; REEVES DIANA C; SENANAYAKE CHRIS H; TANG WENJUN; YEE NATHAN K 权利人:BOEHRINGER INGELHEIM INT; HADDAD NIZAR; KRISHNAMURTHY DHILEEPKUMAR; REEVES DIANA C; SENANAYAKE CHRIS H; TANG WENJUN; YEE NATHAN K 摘要:A method for making the compound of the formula (I), (IV), (VI), (VII) and (VIII), wherein R 1 is C -1-5 -alkyl, C(O)-O benzyl, C(O)-O- tert .butyl or benzyl; and R 2 is C 1 -C 6 alkyl.
专利号:US-2023220001-A1 优先权日:2020-06-09 标 题:Method for synthesis of thioether-containing peptides 发明人:GRUSS HENDRIK; LUTZ CHRISTIAN; SÜSSMUTH RODERICH; Yao guiyang; KNITTEL CAROLINE; KOSOL SIMONE; MAINZ ANDI 权利人:HEIDELBERG PHARMA RES GMBH 摘要:The present invention relates to a method of formation of a sulphur bridge between tryptophan and cysteine in solid phase peptide synthesis under iodine treatment. The invention also relates to the resulting compounds of the method and their respective use.
专利号:US-6380416-B2 优先权日:1997-06-13 标题:Asymmetric synthesis catalyzed by transition metal complexes with rigid chiral ligands 发明人:ZHANG XUMU 权利人:PENN STATE RES FOUND 摘要:This invention is to develop novel transition metal catalysts for the practical synthesis of important chiral molecules. The invention emphasizes asymmetric catalysis based on chiral bidentate phosphine ligands with cyclic ring structures which could be used to restrict conformational flexibility of the ligands and thus the efficiency of chiral transfer can be enhanced through the ligand rigidity.