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(S)-2-diphenylphosphino-1,1'-binaphthyl | 156456-77-8

中文名称
——
中文别名
——
英文名称
(S)-2-diphenylphosphino-1,1'-binaphthyl
英文别名
2-diphenylphosphino-1,1'-binaphthyl;1,1′-binaphthalen-2-yl(diphenyl)phosphine;H-MOP;rac-2-diphenylphosphino-1,1'-binaphthyl;2-(di-tert-butylphosphino)-1,1'-binapthyl;diphenylphosphino-1,1'-binaphthalene;diphenylphosphino-1,1'-binaphthyl;rac-H-MOP;BINAP;(1-naphthalen-1-ylnaphthalen-2-yl)-diphenylphosphane
(S)-2-diphenylphosphino-1,1'-binaphthyl化学式
CAS
156456-77-8
化学式
C32H23P
mdl
——
分子量
438.508
InChiKey
OVPWEQROJNJHAG-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

计算性质

  • 辛醇/水分配系数(LogP):
    8.7
  • 重原子数:
    33
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

SDS

SDS:d046e39bfa7e49d70586dc793ba8adf5
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (S)-2-diphenylphosphino-1,1'-binaphthyl双氧水 、 palladium diacetate 作用下, 以 甲醇三氟乙酸 为溶剂, 反应 1.0h, 生成 2'-(diphenylphosphoryl)-1,1'-binaphthyl-2-yl acetate
    参考文献:
    名称:
    Palladium-catalyzed R2(O)P directed C(sp2)–H acetoxylation
    摘要:
    描述了一种新颖高效的钯催化的C-H乙酰化方法。该方法使用R2(O)P作为导向基团,合成各种取代的2'-磷酸酯联苯-2-OAc化合物。
    DOI:
    10.1039/c4cc01238k
  • 作为产物:
    描述:
    2-溴-1-碘萘 在 bis-triphenylphosphine-palladium(II) chloride 、 正丁基锂potassium carbonate 作用下, 以 乙二醇二甲醚乙醚正己烷 为溶剂, 反应 8.0h, 生成 (S)-2-diphenylphosphino-1,1'-binaphthyl
    参考文献:
    名称:
    Palladium-catalyzed R2(O)P directed C(sp2)–H acetoxylation
    摘要:
    描述了一种新颖高效的钯催化的C-H乙酰化方法。该方法使用R2(O)P作为导向基团,合成各种取代的2'-磷酸酯联苯-2-OAc化合物。
    DOI:
    10.1039/c4cc01238k
  • 作为试剂:
    描述:
    1-丙烯基苯 在 bis(η3-allyl-μ-chloropalladium(II)) 、 三氯硅烷(S)-2-diphenylphosphino-1,1'-binaphthyl 作用下, 以 甲苯 为溶剂, 生成 (R)-1-phenyl-1-(trichlorosilyl)propane 、 (S)-1-phenyl-1-(trichlorosilyl)propane
    参考文献:
    名称:
    Asymmetric Hydrosilylation of Styrenes Catalyzed by Palladium−MOP Complexes:  Ligand Modification and Mechanistic Studies
    摘要:
    In the palladium-catalyzed asymmetric hydrosilylation of styrene (3a) with trichlorosilane, several chiral monophosphine ligands, (R)-2-diarylphosphino-1,1'-binaphthyls(2a-g), were examined for their enantioselectivity. The highest enantioselectivity was observed in the reaction with (R)-2-bis [3,5-bis(trifluoromethyl)phenyl] phosphino-l,1'-binaphthyl (2g), which gave (S)-1-phenylethanol (5a) of 98% ee after oxidation of the hydrosilylation product, 1-phenyl-1-(trichlorosilyl)ethane (4a). The palladium complex of 2g also efficiently catalyzed the asymmetric hydrosilylation of substituted styrenes on the phenyl ring or at the beta position to give the corresponding chiral benzylic alcohols of over 96% ee. Deuterium-labeling studies on the hydrosilylation of regiospecifically deuterated styrene revealed that P-hydrogen elimination from l-phenylethyl(silyl)palladium intermediate is very fast compared with reductive elimination giving hydrosilylation product when ligand 2g is used. The reaction of o-allylstyrene (9) with trichlorosilane catalyzed by (R)-2g/Pd gave (1S,2R)-1-methyl-2-(trichlorosilylmethyl)indan (10) (91% ee) and (S)-1-(2-(propenyl)phenyl)-1-trichlorosilylethanes (11a and 11b) (95% ee). On the basis of their opposite configurations at the benzylic position, a rationale for the high enantioselectivity of ligand 2g is proposed.
    DOI:
    10.1021/jo001614p
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文献信息

  • [EN] ANTHELMINTIC AGENTS AND THEIR USE<br/>[FR] AGENTS ANTHELMINTIQUES ET LEUR UTILISATION
    申请人:INTERVET INT BV
    公开号:WO2010115688A1
    公开(公告)日:2010-10-14
    This invention is directed to compounds and salts that are generally useful as anthelmintic agents or as intermediates in processes for making anthelmintic agents. This invention also is directed to processes for making the compounds and salts, pharmaceutical compositions and kits comprising the compounds and salts, uses of the compounds and salts to make medicaments, and treatments comprising the administration of the compounds and salts to animals in need of the treatments.
    这项发明涉及一般用作驱虫剂或作为制备驱虫剂的中间体的化合物和盐。这项发明还涉及制备这些化合物和盐的方法,包括这些化合物和盐的药物组合物和试剂盒,使用这些化合物和盐制备药物,以及将这些化合物和盐用于需要治疗的动物的治疗方法。
  • [EN] ANTICANCER BENZOPYRAZINES VIA THE INHIBITION OF FGFR KINASES<br/>[FR] BENZOPYRAZINES ANTICANCÉREUSES PAR LE BIAIS DE L'INHIBITION DE FGFR KINASES
    申请人:ASTEX THERAPEUTICS LTD
    公开号:WO2013061081A1
    公开(公告)日:2013-05-02
    The invention relates to new quinoxaline derivative compounds, to pharmaceutical compositions comprising said compounds, to processes for the preparation of said compounds and to the use of said compounds in the treatment of diseases, e.g. cancer.
    这项发明涉及新的喹啉衍生物化合物,包括含有该化合物的药物组合物,用于制备该化合物的方法以及该化合物在治疗疾病(例如癌症)中的用途。
  • Therapeutic heterocyclic compounds
    申请人:——
    公开号:US20030013708A1
    公开(公告)日:2003-01-16
    Provided herein is a compound having the formula (I): 1 Wherein said compounds are useful for the treatment of psychiatric disorders including but not limited to depression, generalized anxiety, eating disorders, dementia, panic disorder, and sleep disorders. The compounds may also be useful in the treatment of gastrointestinal disorders, cardiovascular regulation, motor disorders, endocrine disorders, vasospasm and sexual dysfunction. The compounds are 5HT 1B and 5HT 1D antagonists.
    本文提供的化合物具有以下式(I): 其中所述化合物可用于治疗精神障碍,包括但不限于抑郁症、广泛性焦虑、进食障碍、痴呆症、恐慌障碍和睡眠障碍。这些化合物还可能用于治疗胃肠道障碍、心血管调节、运动障碍、内分泌障碍、血管痉挛和性功能障碍。这些化合物是5HT 1B和5HT 1D拮抗剂。
  • Therapeutic chromone compounds
    申请人:——
    公开号:US20040087575A1
    公开(公告)日:2004-05-06
    Provided herein is a compound of the formula (I) wherein said compound is useful for the treatment of psychiatric disorders including but not limited to depression, generalized anxiety, eating, disorders, dementia, panic disorder, and sleep disorders. The compounds may also be useful in the treatment of gastrointestinal disorders, cardiovascular regulation, motor disorders, endocrine disorders, vasospasm and sexual dysfunction. The compounds are 5HT 1B antagonists. Also provided herein are processes for making compounds of Formula (I) and intermediate compounds.
    本文提供的是一种化合物,其化学式为(I),其中该化合物可用于治疗包括但不限于抑郁症、广泛性焦虑、进食障碍、痴呆症、恐慌障碍和睡眠障碍在内的精神疾病。这些化合物也可能对治疗胃肠道疾病、心血管调节、运动障碍、内分泌失调、血管痉挛和性功能障碍有用。这些化合物是5HT 1B 拮抗剂。本文还提供了制备化合物(I)和中间体化合物的方法。
  • Therapeutic chroman compounds
    申请人:——
    公开号:US20040110745A1
    公开(公告)日:2004-06-10
    Provided herein is a compound represented by the Formula (I) wherein said compounds are useful for the treatment of migraine. Also provided are processes for the preparation of compounds of Formula (I) and intermediates.
    本文提供的是一种化合物,其化学式表示为(I),其中这些化合物对治疗偏头痛有用。还提供了制备化合物(I)和中间体的方法。
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