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

(R)-(+)-2,2'-二(二-3,5-二甲基苯基膦)-5,5',6,6',7,7',8,8'-八氢-1,1'-联萘 | 190003-81-7

中文名称
(R)-(+)-2,2'-二(二-3,5-二甲基苯基膦)-5,5',6,6',7,7',8,8'-八氢-1,1'-联萘
中文别名
(R)-(+)-2,2'-二(二-3,5-二甲基苯基膦)-5,5',6,6',7,7',8,8'-八氢-1,1'-联萘
英文名称
(S)-2,2'-bis[di(3,5-xylyl)phosphino]-5,5',6,6',7,7',8,8'-octahydro-1,1-binaphthyl
英文别名
(S)-xyl-H8-binap;[1-[2-Bis(3,5-dimethylphenyl)phosphanyl-5,6,7,8-tetrahydronaphthalen-1-yl]-5,6,7,8-tetrahydronaphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane
(R)-(+)-2,2'-二(二-3,5-二甲基苯基膦)-5,5',6,6',7,7',8,8'-八氢-1,1'-联萘化学式
CAS
190003-81-7
化学式
C52H56P2
mdl
——
分子量
742.964
InChiKey
MSFLWCTZCJTICH-UHFFFAOYSA-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

物化性质

  • 沸点:
    842.0±65.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    14.6
  • 重原子数:
    54
  • 可旋转键数:
    7
  • 环数:
    8.0
  • 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

文献信息

  • Axially Asymmetric Phosphorus Compound and Production Method Thereof
    申请人:Tanaka Ken
    公开号:US20090227805A1
    公开(公告)日:2009-09-10
    Problem to be Solved: To provide an axially asymmetric optically active biarylphosphorus compound that can easily produced without the step of optical resolution which was almost indispensable in conventional methods. Solution: A method for producing an axially asymmetric phosphorus compound represented by the general formula (1), comprising a cycloaddition reaction of a compound having a triple bond with the use of a catalyst containing rhodium metal and an optically active bisphosphine. (In the formula, J is an oxygen atom, a sulfur atom or BH 3 ; R 1 and R 2 independently are an alkyl, cycloalkyl, aryl, alkoxy and aryloxy group; a1 and a2 independently are 0 or 1; R 3 to R 10 independently are an alkyl, cycloalkyl, aryl, alkoxy and aryloxy group; two among R 3 to R 10 may form a ring; and * is axial asymmetry.)
    要解决的问题:提供一种轴向不对称的光学活性联苯化合物,可以在传统方法中几乎不可或缺的光学分辨步骤之外轻松生产。 解决方案:一种生产由通式(1)表示的轴向不对称化合物的方法,包括使用含有属和光学活性双膦的催化剂进行含有三键化合物的环加成反应。 (在公式中,J是氧原子、原子或BH3;R1和R2独立地是烷基、环烷基、芳基、烷氧基和芳氧基;a1和a2独立地为0或1;R3到R10独立地是烷基、环烷基、芳基、烷氧基和芳氧基;R3到R10中的两个可能形成环;*表示轴向不对称。)
  • PROCESS FOR PRODUCING OPTICALLY ACTIVE AMINE
    申请人:TAKASAGO INTERNATIONAL CORPORATION
    公开号:US20150210657A1
    公开(公告)日:2015-07-30
    A process for producing an optically active amine compound, characterized by asymmetrically hydrogenating a prochiral carbon-nitrogen double bond in the presence of a ruthenium complex represented by general formula (1) or (2) (wherein P represents an optically active diphosphine, X represents an anionic group, and Ar represents an optionally substituted arylene group).
    一种制备光学活性胺化合物的方法,其特征在于在存在由通用式(1)或(2)表示的配合物的情况下,对一个丙半胱基双键进行不对称氢化(其中P代表光学活性二膦,X代表阴离子基团,Ar代表可选择取代的芳基基团)。
  • Axially asymmetric ester compound and production method thereof
    申请人:Tanaka Ken
    公开号:US20090299076A1
    公开(公告)日:2009-12-03
    To provide an axially asymmetric optically active biaryl ester compound that can easily produced without the step of optical resolution which was almost indispensable in conventional methods. There is provided a method for producing an axially asymmetric ester compound, comprising a cycloaddition of a compound having a triple bond with the use of a catalyst containing rhodium metal and an optically active bisphosphine.
    提供一种具有轴向不对称光学活性的双芳基酯化合物,可在传统方法中几乎不可或缺的光学分辨步骤之外轻松生产。提供了一种生产轴向不对称酯化合物的方法,包括使用含有属和光学活性双膦催化剂对具有三键的化合物进行环加成。
  • IRIDIUM COMPLEXES
    申请人:Mashima Kazushi
    公开号:US20090036696A1
    公开(公告)日:2009-02-05
    The present invention has as its object to provide an iridium complex represented by the general formula: [(l r H L 1 L 2 ) 2 (μ-X 1 )(μ-X 2 )(μ-X 3 )]X 4 (1) (wherein L 1 and L 2 may be the same or different and each represent a monodendate neutral ligand, or each cooperate with the other to form a bidendate neutral ligand; X 1 , X 2 and X 3 may be the same or different, and each represent a halogen atom; and X 4 is a counter-anion). Also, the present invention provides a novel catalyst which can achieve excellent performance as a catalyst for asymmetric synthesis, especially asymmetric hydrogenation, in terms of chemical selectivity, enantioselectivity and catalytic activity, and the like.
    本发明的目的是提供一种配合物,其通式表示为:[(l r H L1L2)2(μ-X1)(μ-X2)(μ-X3)]X4(1)(其中L1和L2可以相同也可以不同,每个代表一种单齿中性配体,或者合作形成一种双齿中性配体;X1、X2和X3可以相同也可以不同,每个代表一种卤素原子;X4是一个反离子)。此外,本发明提供了一种新型催化剂,可以在化学选择性、对映选择性和催化活性等方面实现出色的性能,特别是作为不对称合成的催化剂,尤其是不对称氢化反应。
  • Process for producing optically active-3-quinuclidinols
    申请人:Takenaka Motonobu
    公开号:US20060047122A1
    公开(公告)日:2006-03-02
    An object of the present invention is to provide a process for producing optically active 3-quinuclidinol having high optical purity or the salt thereof at high yield. The invention relates to a process for producing optically active 3-quinuclidinol or the salt thereof by reacting 3-quinuclidinone or the salt thereof with hydrogen in the presence of a basic compound, a complex of a transition metal in Groups 8 to 10, an optically active bidentate ligand and an optically active diamine.
    本发明的目的是提供一种制备具有高光学纯度或其盐的光学活性3-喹诺醇的高产率工艺。该发明涉及一种通过在碱性化合物、8至10族过渡属的配合物、光学活性双齿配体和光学活性二胺的存在下,将3-喹诺酮或其盐与氢反应来制备光学活性3-喹诺醇或其盐的工艺。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫