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(1R,2R)-N,N'-bis[(1-naphthyl)-methyl]-1,2-diaminocyclohexane

中文名称
——
中文别名
——
英文名称
(1R,2R)-N,N'-bis[(1-naphthyl)-methyl]-1,2-diaminocyclohexane
英文别名
(1R,2R)-N1,N2-bis(naphthalen-1-ylmethyl)cyclohexane-1,2-diamine;(R,R)-N,N’-bis(1-naphthylmethyl)cyclohexane-1,2-diamine;(R,R)-1,2-di(1-naphthyl-CH2NH)cyclohexane;(1R,2R)-1-N,2-N-bis(naphthalen-1-ylmethyl)cyclohexane-1,2-diamine
(1R,2R)-N,N'-bis[(1-naphthyl)-methyl]-1,2-diaminocyclohexane化学式
CAS
——
化学式
C28H30N2
mdl
——
分子量
394.56
InChiKey
MOFAWJAXQCZGDZ-VSGBNLITSA-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):
    6.2
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    24.1
  • 氢给体数:
    2
  • 氢受体数:
    2

上下游信息

  • 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:
    参考文献:
    名称:
    Group-Assisted Purification (GAP) for Protection of Amino Acids Using N-Phosphonyl Functional Groups
    摘要:
    Various phosphonyl halides have been synthesized and utilized as protection groups for amino acids. The protection synthesis was performed via GAP (Group-Assisted Purification) procedure under convenient conditions without the use of column chromatography and recrystallization. The synthesis can be carried out on applicational scales with excellent yields (82% - 98%). The phosphonyl protection of amino acids would provide a new greener tool for GAP peptide synthesis.
    DOI:
    10.3987/com-14-s(k)25
  • 作为产物:
    描述:
    (1R,2R)-bis-1-naphthyliminocyclohexane 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 以88%的产率得到(1R,2R)-N,N'-bis[(1-naphthyl)-methyl]-1,2-diaminocyclohexane
    参考文献:
    名称:
    N-杂环卡宾介导的苯酚对不对称烷基芳基烯酮的对映选择性加成
    摘要:
    手性N-杂环卡宾(NHC)介导将2-苯基苯酚对映选择性加成到不对称的烷基芳基烯酮中,从而提供具有良好对映体控制水平的ee-烷基-α-芳酸衍生物(最高ee达84%)。在NHC促进的酯化反应中使用2-苯基苯酚和二氢苯酚,使用衍生自焦谷氨酸的三唑鎓预催化剂观察到对映体立体化学结果,这与这些过程中起作用的独特机理相符。
    DOI:
    10.1002/adsc.200900538
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文献信息

  • Asymmetric allylation reactions of aromatic aldehydes with allyltrichlorosilane catalyzed by chiral bisformamide-type organocatalysts
    作者:Yuya Tanimura、Kaori Ishimaru
    DOI:10.1016/j.tetasy.2012.02.015
    日期:2012.3
    Asymmetric allylation reactions of aromatic aldehydes with allyltrichlorosilane were catalyzed by C2-symmetrical chiral bisformamides in the presence of potassium carbonate and potassium phosphate, to afford the corresponding homoallylic alcohols in excellent yields with up to 83% ee.
    在碳酸钾和磷酸钾存在下,C 2对称手性双甲酰胺催化芳族醛与烯丙基三氯硅烷的不对称烯丙基化反应,从而以极高的收率得到相应的均烯丙基醇,ee最高可达83%。
  • Highly selective R,S-coordination of non racemic (1R,2R)-(1,2-dialkyl)-1,2-diamine cyclohexane derivatives to palladium dichloride
    作者:Esfandiar Rafii、Benjamin Dassonneville、Andreas Heumann
    DOI:10.1039/b613961b
    日期:——
    In non-racemic (1R,2R)-(1,2-dialkyl)-1,2-diaminocyclohexane palladium dichloride complexes the C2 symmetry of the diamine ligand is broken, resulting in selective R,S-coordination.
    在非外消旋的(1R,2R)-(1,2-二烷基)-1,2-二氨基环己烷二氯化钯配合物中,二胺配体的C2对称性被破坏,导致选择性的R,S配位。
  • N-Heterocyclic Carbene-Mediated Enantioselective Addition of Phenols to Unsymmetrical Alkylarylketenes
    作者:Carmen Concellón、Nicolas Duguet、Andrew D. Smith
    DOI:10.1002/adsc.200900538
    日期:2009.11
    Chiral N-heterocyclic carbenes (NHCs) mediate the enantioselective addition of 2-phenylphenol to unsymmetrical alkylarylketenes, delivering α-alkyl-α-arylacetic acid derivatives with good levels of enantiocontrol (up to 84% ee). Enantiodivergent stereochemical outcomes are observed using 2-phenylphenol and benzhydrol in the NHC-promoted esterification reaction using a triazolium precatalyst derived
    手性N-杂环卡宾(NHC)介导将2-苯基苯酚对映选择性加成到不对称的烷基芳基烯酮中,从而提供具有良好对映体控制水平的ee-烷基-α-芳酸衍生物(最高ee达84%)。在NHC促进的酯化反应中使用2-苯基苯酚和二氢苯酚,使用衍生自焦谷氨酸的三唑鎓预催化剂观察到对映体立体化学结果,这与这些过程中起作用的独特机理相符。
  • Synthesis of N,N′-Dialkylated Cyclohexane-1,2-diamines and Their Application as Asymmetric Ligands and Organocatalysts for the Synthesis of Alcohols
    作者:Denis Chusov、Alexey Tsygankov、Man-Seog Chun、Alexandra Samoylova、Seongyeon Kwon、Yuliya Kreschenova、Suhyeon Kim、Euijin Shin、Jinho Oh、Tatyana Strelkova、Valerii Kolesov、Fedor Zubkov、Sergei Semenov、Ivan Fedyanin
    DOI:10.1055/s-0036-1588382
    日期:——
    A series of N,N′-dialkylated derivatives of (1R,2R)-cyclohexane-1,2-diamine were synthesized, and a new approach to the one-pot preparation of this type of amine was demonstrated. The prepared diamines were used as organocatalysts for the two-step synthesis of α-hydroxy γ-keto esters from arenes, chlorooxoacetates, and ketones; they were also used as chiral ligands for Meervein–Ponndorf–Verley reductions
    合成了一系列(1R,2R)-环己烷-1,2-二胺的N,N'-二烷基化衍生物,并展示了该类胺的一锅法制备新方法。制备的二胺用作有机催化剂,用于从芳烃、氯代乙酸酯和酮两步合成α-羟基γ-酮酯;它们也被用作 Meervein-Ponndorf-Verley 还原和亨利反应的手性配体。
  • HFIP‐Promoted Substitution in the Ferrocene Series: Smooth Approach towards Original Catalysts**
    作者:William Erb、Victor Carré、Thierry Roisnel
    DOI:10.1002/ejoc.202100824
    日期:2021.11.8
    Pseudo-benzylic substitution promoted by fluorinated solvent from various iodoferrocenes is described. These new reaction conditions allow the fast generation of libraries of derivatives for applications in catalysis for example, as demonstrated with the synthesis of original ligands used in cross-coupling reactions.
    描述了由来自各种碘二茂铁的氟化溶剂促进的伪苄基取代。这些新的反应条件允许快速生成用于催化应用的衍生物库,例如,如交叉偶联反应中使用的原始配体的合成所证明的那样。
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