摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[(2R)-2-Cyclohexyl-2-(3H-inden-1-yl)ethyl]diphenylphosphine | 497869-48-4

中文名称
——
中文别名
——
英文名称
[(2R)-2-Cyclohexyl-2-(3H-inden-1-yl)ethyl]diphenylphosphine
英文别名
[(2R)-2-cyclohexyl-2-(3H-inden-1-yl)ethyl]-diphenylphosphane
[(2R)-2-Cyclohexyl-2-(3H-inden-1-yl)ethyl]diphenylphosphine化学式
CAS
497869-48-4
化学式
C29H31P
mdl
——
分子量
410.539
InChiKey
WCPLVVFKLVLVLT-GDLZYMKVSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    7.9
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    di(rhodium)tetracarbonyl dichloride 、 [(2R)-2-Cyclohexyl-2-(3H-inden-1-yl)ethyl]diphenylphosphine 在 n-BuLi 作用下, 以 四氢呋喃正己烷 为溶剂, 以36%的产率得到(η5:η1-indenyl-CH(Cy)CH2PPh2)Rh(CO)
    参考文献:
    名称:
    Induction of Planar Chirality in Formation of (η51-1-(1-Cyclohexyl-2-(diphenylphosphino)ethyl)indenyl)carbonylrhodium and (η51-1-(2-Phenyl-2- (diphenylphosphino)ethyl)indenyl)carbonylrhodium
    摘要:
    The enantiopure bidentate indenyl-phosphine ligands (1S)-[2-(3H-inden-1-yl)-1-phenylethyl] diphenylphosphine (9) and [(2R)-2-cyclohexyl-2-(3H-inden-1-yl)ethyl]diphenylphosphine (18) were synthesized in 20% yield and three steps from (R)-styrene oxide and in 61% yield and four steps from vinylcyclohexane, respectively. In both cases ring opening of a spirocyclopropane-1,1'-indene with potassium diphenylphosphide was a key step. Addition of the lithium salts of 9 and 18 to [Rh(mu -Cl)(CO)(2)](2) gave (eta (5):eta (1)-indenyl-CH2CH(Ph)PPh2)RhCO and (eta (5):eta (1)-indenyl-CH(Cy)CH2PPh2)RhCO as 75:25 and 78:22 mixtures of diastereoisomers, from which the major complexes were readily obtained by crystallization. The chiral centers in the linking chain beta and alpha to the indenyl ring had thus induced good planar chirality of the complexed indenyl moiety. Both complexes were characterized by X-ray crystallography.
    DOI:
    10.1021/om010367s
点击查看最新优质反应信息

文献信息

  • Erythropoietin production accelerator
    申请人:Imagawa Shigehiko
    公开号:US20060040986A1
    公开(公告)日:2006-02-23
    The present invention relates to a preventive or therapeutic agent for pathological conditions caused by reduced production of erythropoietin, or for anemia, or for chronic anemia, renal anemia, aplastic anemia, or pure red cell aplasia, the agent comprising, as an active ingredient, a cyclic amine compound represented by the following formula (1): wherein, R 1 , R 2 and R 3 each independently represent a hydrogen atom, a halogen atom, or hydroxy, alkyl, halogen-substituted alkyl, alkoxy, alkylthio, carboxyl, alkoxycarbonyl or alkanoyl group; W 1 and W 2 each independently represent N or CH; X represents O, NR 4 , CONR 4 or NR 4 CO; R 4 each represents a hydrogen atom, or an alkyl, alkenyl, alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, or substituted or unsubstituted heteroaralkyl group; and l, m and n each represents a number of 0 or 1, or a salt thereof or a solvate thereof.
    本发明涉及一种预防或治疗由于红细胞生成素减少引起的病理状态,或用于贫血,慢性贫血,肾性贫血,再生障碍性贫血或纯红细胞再生障碍的药物,该药物包含以下式(1)所表示的环状胺化合物作为活性成分:其中,R1,R2和R3各自独立地表示氢原子,卤素原子,羟基,烷基,卤代烷基,烷氧基,烷基,羧基,烷氧羰基或烷酰基;W1和W2各自独立地表示N或CH;X表示O,NR4,CONR4或NR4CO;R4表示氢原子,或烷基,烯基,炔基,取代或未取代芳基,取代或未取代杂芳基,取代或未取代芳基甲基,或取代或未取代杂芳基甲基基团;l,m和n各自表示0或1的数字,或其盐或溶剂化物。
  • ERYTHROPOIETIN PRODUCTION ACCELERATOR
    申请人:Kowa Co., Ltd.
    公开号:EP1568691A1
    公开(公告)日:2005-08-31
    The present invention relates to a preventive or therapeutic agent for pathological conditions caused by reduced production of erythropoietin, or for anemia, or for chronic anemia, renal anemia, aplastic anemia, or pure red cell aplasia, the agent comprising, as an active ingredient, a cyclic amine compound represented by the following formula (1): wherein,    R1, R2 and R3 each independently represent a hydrogen atom, a halogen atom, or hydroxy, alkyl, halogen-substituted alkyl, alkoxy, alkylthio, carboxyl, alkoxycarbonyl or alkanoyl group;    W1 and W2 each independently represent N or CH;    X represents O, NR4, CONR4 or NR4CO;    R4 each represents a hydrogen atom, or an alkyl, alkenyl, alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted aralkyl, or substituted or unsubstituted heteroaralkyl group; and    l, m and n each represents a number of 0 or 1, or a salt thereof or a solvate thereof.
    本发明涉及一种预防或治疗剂,用于治疗因促红细胞生成素生成减少而引起的病理状况,或用于治疗贫血,或用于治疗慢性贫血、肾性贫血、再生障碍性贫血或单纯红细胞增生症,该剂作为一种活性成分,包括由下式(1)代表的环胺类化合物: 其中 R1、R2 和 R3 各自独立地代表氢原子、卤素原子或羟基、烷基、卤素取代的烷基、烷氧基、烷基、羧基、烷氧羰基或烷酰基; W1 和 W2 各自独立地代表 N 或 CH; X 代表 O、NR4、CONR4 或 NR4CO; R4 各自代表氢原子或烷基、烯基、炔基、取代或未取代的芳基、取代或未取代的杂芳基、取代或未取代的芳烷基或取代或未取代的杂烷基;以及 l、m 和 n 各代表 0 或 1,或其盐或其溶液。
  • CHIRAL ORGANOMETALLIC COMPOUNDS FOR USE IN ASYMMETRIC SYNTHESIS
    申请人:Avecia Limited
    公开号:EP1417030A1
    公开(公告)日:2004-05-12
  • US7019158B1
    申请人:——
    公开号:US7019158B1
    公开(公告)日:2006-03-28
  • [EN] CHIRAL ORGANOMETALLIC COMPOUNDS FOR USE IN ASYMMETRIC SYNTHESIS<br/>[FR] COMPOSES ORGANOMETALLIQUES CHIRAUX S'UTILISANT DANS UNE SYNTHESE ASYMETRIQUE
    申请人:AVECIA LTD
    公开号:WO2003013724A1
    公开(公告)日:2003-02-20
    Chiral organometallic compounds are provided which comprise certain non-symmetrically substituted cyclopentadiene complexed to a transition metal. The cyclopentadiene has a second coordinating group which also complexes the transition metal and is attached to the cyclopentadiene by means of a chiral connecting chain. Preferred transition metals include rhodium, ruthenium, iridium, cobalt, iron, manganese, chromium, tungsten, molybdenum, nickel, palladium, or platinum. These chiral organometallic compounds find use in asymmetric synthesis to produce chiral compounds.
查看更多

同类化合物

(2′′-甲基氨基-1,1′′-联苯-2-基)甲烷磺酰基铝(II)二聚体 马来酸二甲茚定 螺[茚-1,4’-哌啶]盐酸盐 螺[茚-1,4-哌啶] 螺[1H-茚-1,4-哌啶]-3-羧酸盐酸盐 螺[1H-茚-1,4-哌啶]-1,3-二羧酸,1,1-二甲基乙酯 螺[1,3-二氧戊环-2,1'-茚] 萘,3-溴-2-氯-1,2-二氢-1,1-二甲基- 茚洛秦 茚旦醇 茚并[2,1-a]茚 茚屈林 茚-2,3-二羧酸 苯酚,2-(1H-茚-3-基)- 苯茚达明酒石酸盐 苯茚胺 苯基亚甲基双(三环己基磷)二氯化钌 膦,1H-茚-1-基二苯基- 硬树脂 硫化舒林酸 硫化舒林酸 盐酸茚诺洛尔 盐酸茚洛秦 盐酸苯二胺 甲茚 甲基3-氨基-1H-茚-2-羧酸酯 甲基3-氨基-1-氰基-1-苯基-1H-茚-2-羧酸酯 甲基1-氧代-2-苯基-1H-茚-3-基碳酸酯 氰基酰胺,(2,3-二氯-1,4-萘二亚基)二-,(E,E)- 氨甲酸,[(1S)-1-甲基-2-(硝基氧代)乙基]-,1,1-二甲基乙基酯(9CI) 异苯茚达明 尿苷,2'-脱氧-5-(2-羟基乙基)-,3',5'-二(4-甲基苯酸酯)(9CI) 外消旋-N-去甲基二甲茚定 四氢荧蒽 四-1H-茚-1-ylstannane 吡喃达明盐酸盐 吡喃达明 叔-丁基6-甲基螺[茚并-1,4-哌啶]-1-甲酸基酯 叔-丁基6-氯螺[茚并-1,4-哌啶]-1-甲酸基酯 全氟(3-甲基茚) 亚乙基二(4,5,6,7-四氢-1-茚基)二甲基锆(IV) 二茚并[1,2-b:2,1-e]吡啶-10,12-二酮,5,11-二氢-5-甲基- 二苯并[A,E]环辛烯,5,11-双(苯磺酰基) 二甲茚定 二甲基亚甲硅烷基)双(2-甲基-4-苯基茚基)二氯化锆 二甲基[二(2-甲基-1H-茚-1-基)]硅烷 二甲基-(2-吗啉-4-基-茚-1-亚基甲基)-胺 二环己基[2-(2,4,6-三甲基苯基)-1H-茚-3-基]膦 二乙基-[2-(3-异丙基-1-苯基-茚-1-基)-乙基]-胺