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(1S,2R)-1-butyryloxymethyl-2-formylcyclopropane | 566928-18-5

中文名称
——
中文别名
——
英文名称
(1S,2R)-1-butyryloxymethyl-2-formylcyclopropane
英文别名
[(1S,2R)-2-formylcyclopropyl]methyl butanoate
(1S,2R)-1-butyryloxymethyl-2-formylcyclopropane化学式
CAS
566928-18-5
化学式
C9H14O3
mdl
——
分子量
170.208
InChiKey
BNQJVVOQNFBEPP-JGVFFNPUSA-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):
    0.8
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

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

反应信息

点击查看最新优质反应信息

文献信息

  • The synthesis of (11R,12S)-lactobacillic acid and its enantiomer
    作者:Geoffrey D. Coxon、Juma R. Al-Dulayymi、Mark S. Baird、Stefan Knobl、Evan Roberts、David E. Minnikin
    DOI:10.1016/s0957-4166(03)00165-4
    日期:2003.5
    (11R,12S)-Lactobacillic acid has been prepared from 2,3-O-isopropylidene-D-glyceraldehyde, in a sequence involving asymmetric cyclopropanation, and from cis-cyclopropane-1,2-dimethanol, using enzymatic desymmetrisation. The key step in the former route was the stereochemically controlled cyclopropanation of (1Z,4'S)-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-1-octene via a Simmons-Smith type reaction, using diethylzinc and chloroiodomethane. This product was converted into the key intermediate (1R,2S)-1-formyl-2-hexylcyclopropane, which was also obtained by a known sequence from the (1R,2S)-monobutyrate ester of cis-cyclopropane-1,2-dimethanol. This pivotal aldehyde was converted into (11R,12S)-lactobacillic acid. Using analogous chemistry, the (11S,12R)-enantiomer of lactobacillic acid was prepared from 2,3-O-isopropylidene-D-glyceraldehyde or from the (1S,R)-monobutyrate ester of cis-cyclopropane-1,2-dimethanol. (C) 2003 Elsevier Science Ltd. All rights reserved.
    (LS,12S)-乳酸杆菌酸已从2,3-O异丙烯基-D-甘油醛中制备,其中涉及非对映异构物环丙烷化,以及从顺式环丙烷-1,2-二甲醇中使用酶催化去对称化。前一条路线的关键步骤是通过对(1Z,4S')-(2',2'-二甲基-1',3'-二氧杂环戊烷-4'-基)-1-辛烯进行Simmons-Smith型反应进行立体化学控制的环丙烷化,使用了二乙基锌和碘氯甲烷。该产品被转化为关键中间体(1R,2S)-1-甲酰基-2-己基环丙烷,该中间体也可通过已知路线从顺式环丙烷-1,2-二甲醇的(1R,2S)-单丁酸酯获得。这种关键的醛被转化为(11R,12S)-乳酸杆菌酸。通过类似化学,乳酸杆菌酸的(11S,12R)-对映异构体从2,3-O异丙烯基-D-甘油醛或顺式环丙烷-1,2-二甲醇的(1S,R)-单丁酸酯中制备。 (C) 2003 Elsevier Science Ltd. 保留所有权利。
  • The synthesis of single enantiomers of a meromycolic acid
    作者:Juma'a R Al Dulayymi、Mark S Baird、Evan Roberts
    DOI:10.1016/s0040-4039(00)01147-3
    日期:2000.9
    3-Oxa-2,4-dioxobicyclo[3.1.0]hexane provides a flexible starting material for the preparation of single enantiomers of a meromycolic acid, a long chain fatty acid containing two remote cis-cyclopropanes.
    3-Oxa-2,4-二氧代双环[3.1.0]己烷提供了一种灵活的原料,用于制备单山co酸(一种含有两个远端顺式环丙烷的长链脂肪酸)的对映体。
  • The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis
    作者:Juma'a R. Al Dulayymi、Mark S. Baird、Evan Roberts
    DOI:10.1016/j.tet.2005.09.056
    日期:2005.12
    We report a synthesis of a single enantionner of a mycolic acid from Mycobacterium tuberculosis containing a di-cis-cyclopropane. The method can be simply varied to modify the chain lengths or the absolute stereochemistry of either cyclopropane. (c) 2005 Elsevier Ltd. All fights reserved.
  • The first syntheses of single enantiomers of the major methoxymycolic acid of Mycobacterium tuberculosis
    作者:Juma'a R. Al Dulayymi、Mark S. Baird、Evan Roberts、Madrey Deysel、Jan Verschoor
    DOI:10.1016/j.tet.2007.01.007
    日期:2007.3
    The synthesis of three stereoisomers of a major homologue of the methoxymycolic acids present in Mycobacterium tuberculosis is described. (c) 2007 Elsevier Ltd. All rights reserved.
  • The absolute stereochemistry of cascarillic acid
    作者:Ieuan O. Roberts、Mark S. Baird、Ying Liu
    DOI:10.1016/j.tetlet.2004.09.141
    日期:2004.11
    ((1S,2R)-2-Hexylcycloprop-1-yl)acetic acid has been synthesised from cis-1,2-dihydroxymethylcyclopropane and shown to be identical to cascarillic acid obtained from cascarilla essential oil. (C) 2004 Elsevier Ltd. All rights reserved.
    ((1S,2R)-2-己基环丙-1-基)乙酸已从顺式-1,2-二羟甲基环丙烷成功合成,并已被证实与从檫木属精油中获得的卡莎林酸相同。(C)2004 Elsevier Ltd. 版权所有。
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