(S)-binapine

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (S)-binapine
• 英文别名: binapine；(12R,13S)-13-tert-butyl-12-[(12R,13S)-13-tert-butyl-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-12-yl]-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaene
• 化学式: C₅₂H₄₈P₂
• 分子量: 734.901
• InChiKey: YXMFQIWDFKIXGQ-MEJQTXDZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  12.1
• 重原子数：
  54
• 可旋转键数：
  3
• 环数：
  10.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

文献信息

• METHODS FOR ENANTIOSELECTIVE ALLYLIC ALKYLATION OF ESTERS, LACTONES, AND LACTAMS WITH UNACTIVATED ALLYLIC ALCOHOLS
  申请人：Stoltz Brian M.

  公开号：US20190135754A1

  公开（公告）日：2019-05-09

  The present disclosure provides methods for enantioselective synthesis of cyclic and acyclic α-quaternary carboxylic acid derivatives via nickel-catalyzed allylic alkylation.

  本公开提供了一种通过镍催化的烯丙基烷基化方法，用于对环状和非环状α-季铵羧酸衍生物进行对映选择性合成。
• COBALT PHOSPHINE ALKYL COMPLEXES FOR THE ASYMMETRIC HYDROGENATION OF ALKENES
  申请人：The Trustees of Princeton University

  公开号：US20130281747A1

  公开（公告）日：2013-10-24

  Disclosed herein are manganese, iron, nickel, or cobalt compounds having a bidentate ligand and the use of these compounds for the hydrogenation of alkenes, particularly the asymmetric hydrogenation of prochiral olefins.

  本文披露了具有双齿配体的锰、铁、镍或钴化合物，以及这些化合物在烯烃的加氢反应中的应用，特别是对前手性烯烃的不对称加氢。
• [EN] PROCESS FOR PREPARING AN UNSATURATED CARBOXYLIC ACID SALT USING AN ARYLOXIDE<br/>[FR] PROCÉDÉ DE PRÉPARATION D'UN SEL D'ACIDE CARBOXYLIQUE INSATURÉ À L'AIDE D'UN OXYDE D'ARYLE
  申请人：BASF SE

  公开号：WO2015173277A1

  公开（公告）日：2015-11-19

  Catalytic process for preparing an α,β-ethylenically unsaturated carboxylic acid salt, wherein an alkene and carbon dioxide are reacted in the presence of a carboxylation catalyst and in the presence of a specific aryloxide to obtain the α,β-ethylenically unsaturated carboxylic acid salt, the carboxylation catalyst being a transition metal complex. The process allows for efficient preparation of α,β-ethylenically unsaturated carboxylic acid derivatives from CO2 and an alkene.

  该催化过程用于制备α，β-乙烯基不饱和羧酸盐，其中在羧化催化剂和特定芳基氧化物的存在下，烯烃和二氧化碳反应，从而获得α，β-乙烯基不饱和羧酸盐，羧化催化剂是过渡金属配合物。该过程允许从CO2和烯烃高效制备α，β-乙烯基不饱和羧酸衍生物。
• [EN] PROCESS FOR PREPARING AN UNSATURATED CARBOXYLIC ACID SALT<br/>[FR] PROCÉDÉ DE PRÉPARATION D'UN SEL D'ACIDE CARBOXYLIQUE INSATURÉ
  申请人：BASF SE

  公开号：WO2015173276A1

  公开（公告）日：2015-11-19

  Catalytic process for preparing an α,β-ethylenically unsaturated carboxylic acid salt, comprising reacting an alkene and carbon dioxide in the presence of a carboxylation catalyst and releasing the α,β-ethylenically unsaturated carboxylic acid salt with a base, the carboxylation catalyst being a transition metal complex, which comprises a structurally constrained bidentate P,X ligand, wherein X is selected from the group consisting of P, N, O, and carbene, the P and X atom are separated by 2 to 4 bridging atoms, and wherein the bridging atoms are part of at least one 5- to 7-membered cyclic substructure. A further catalytic processes for preparing α,β-ethylenically unsaturated carboxylic acid derivatives from CO2 and an alkene is provided.

  制备α，β-乙烯基不饱和羧酸盐的催化过程，包括在羧化催化剂的存在下，将烯烃和二氧化碳反应，并用碱释放α，β-乙烯基不饱和羧酸盐，其中羧化催化剂是过渡金属配合物，包括结构上限制的双齿P，X配体，其中X选自P，N，O和卡宾的群体，P和X原子之间由2到4个桥接原子分隔开来，且桥接原子是至少一个5到7成员环亚结构的一部分。还提供了另一种从CO2和烯烃制备α，β-乙烯基不饱和羧酸衍生物的催化过程。
• Enantioselective synthesis of 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo[4,5,1-JK][1]-benzazepin-2[1H]-one and zilpaterol
  申请人：Almena-Perea Juan Jose

  公开号：US20100173892A1

  公开（公告）日：2010-07-08

  This invention relates to a process for the hydrogenation of a ketooxime to selectively form an aminoalcohol stereoisomer, and, in particular, to a process for the hydrogenation of 4,5-dihydro-imidazo[4,5,1-jk][1]benzazepin-2,6,7[1H]-trione-6-oxime or a salt thereof to selectively form a stereoisomer of 6-amino-7-hydroxy-4,5,6, 7-tetrahydro-imidazo[4,5,1-jk][1]-benzazepin-2[1H]-one or a salt thereof. This invention also relates to the use of the 6-amino-7-hydroxy-4,5,6,7-tetrahydro-imidazo[4,5,1-jk][1]-benzazepin-2[1H]-one hydrogenation product or a salt thereof to selectively make a stereoisomer of zilpaterol or a salt thereof, as well as the use of such a zilpaterol stereoisomer or salt in methods of treatment and medicaments for animals.

  本发明涉及一种氢化酮肟的方法，以选择性地形成氨基醇立体异构体，特别是涉及一种对4,5-二氢咪唑[4,5,1-jk][1]苯并氮杂环-2,6,7[1H]-三酮-6-肟或其盐进行氢化的方法，以选择性地形成6-氨基-7-羟基-4,5,6,7-四氢咪唑[4,5,1-jk][1]-苯并氮杂环-2[1H]-酮或其盐的立体异构体。本发明还涉及使用6-氨基-7-羟基-4,5,6,7-四氢咪唑[4,5,1-jk][1]-苯并氮杂环-2[1H]-酮氢化产物或其盐选择性地制备一种齐帕特罗尔的立体异构体或其盐，以及使用这种齐帕特罗尔立体异构体或其盐在动物治疗和药物中的方法。