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<(4-Chlorophenyl)sulfinyl>acetic acid | 69529-90-4

中文名称
——
中文别名
——
英文名称
<(4-Chlorophenyl)sulfinyl>acetic acid
英文别名
(R)-4-chlorophenylsulfinylacetic acid;2-[(R)-(4-chlorophenyl)sulfinyl]acetic acid
<(4-Chlorophenyl)sulfinyl>acetic acid化学式
CAS
69529-90-4
化学式
C8H7ClO3S
mdl
——
分子量
218.661
InChiKey
BGQBJZGWNGYNEP-CYBMUJFWSA-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):
    1.4
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    73.6
  • 氢给体数:
    1
  • 氢受体数:
    4

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

  • 作为反应物:
    描述:
    <(4-Chlorophenyl)sulfinyl>acetic acid三氯溴甲烷 作用下, 以 二氯甲烷 为溶剂, 反应 0.58h, 生成 (S)-1-((bromomethyl)sulfinyl)-4-chlorobenzene
    参考文献:
    名称:
    α-亚磺酰酯的酶促分离和脱羧官能团化
    摘要:
    α-亚爷酯的酶促分离得到具有高对映体纯度的回收酯和 α-亚爷酸。脱羧官能团化提供了两种对映体形式的多种光学活性亚砜。
    DOI:
    10.1002/chem.202302996
  • 作为产物:
    描述:
    methyl 4-chlorophenylsulfinylacetate 作用下, 以 甲苯 为溶剂, 反应 25.0h, 生成 <(4-Chlorophenyl)sulfinyl>acetic acid 、 (S)-(-)-<(4-Chlorophenyl)sulfinyl>acetic acid
    参考文献:
    名称:
    Biocatalytic resolutions of sulfinylalkanoates: a facile route to optically active sulfoxides
    摘要:
    Two methods are presented for kinetic resolutions of compounds containing ester and sulfoxide functionalities (sulfinylalkanoates). In the first a crude lipase preparation from Pseudomonas sp. (K10) mediates enantioselective hydrolysis of these esters in an aqueous environment. The second method uses the same lipase preparation to promote enantioselective transesterifications with alcohols in hexane. Both procedures are suitable for preparation of sulfinylalkanoates where the ester and sulfoxide groups are separated by one or two methylene units (sulfinylacetates and sulfinylpropanoates) but compounds with three methylene "spacer groups" (sulfinylbutanoates) are not substrates for the lipase under either set of conditions.
    DOI:
    10.1021/jo00030a044
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文献信息

  • A facile route to homochiral sulfoxides
    作者:Kevin Burgess、Ian Henderson
    DOI:10.1016/s0040-4039(01)80467-6
    日期:1989.1
    Biocatalytic resolutions of methyl sulfinylacetates fford sulfoxides (R)-(1) - (6) in very high optical yields; the products have been used in a systematic study of the “SPAC” reaction, an asymmetric synthesis of γ-hydroxy-α,β-unsaturated esters.
    以非常高的光学收率得到亚甲基乙酸乙酸甲酯和亚砜(R)-(1)-(6)的生物催化拆分;该产品已用于系统研究“ SPAC”反应,即不对称合成γ-羟基-α,β-不饱和酯。
  • Stereochemically matched sulfinylacetates for double diastereoselection in the spac reaction
    作者:Kevin Burgess、Ian Henderson
    DOI:10.1016/s0040-4020(01)82313-9
    日期:1991.8
    which the sulfoxide asymmetry is matched with the inducing effect of the auxiliary give good diastereoselection in SPAC reactions affording γ-hydroxy-α,β-unsaturatod alcohols of high optical purity. Asymmetry at the sulfoxide has a greater effect than the auxiliaries on the stereochemical outcome of these reactions.
    从单手性醇制备具有确定的立体化学的4-氯苯基亚磺酰基乙酸酯:化合物(2)来自(+)-薄荷醇;(-)-8-苯基薄荷醇中的3和4;(+)-反式-2-苯基环己醇的5和6 ; (7)和(9)来自(-)-10-二环己基氨磺酰基-D-异冰片醇。亚砜不对称性与助剂的诱导作用相匹配的试剂在SPAC反应中具有良好的非对映选择性,从而提供了具有高光学纯度的γ-羟基-α,β-不饱和醇。亚砜的不对称性比助剂对这些反应的立体化学结果的影响更大。
  • Biocatalytic resolutions of sulfinylalkanoates: a facile route to optically active sulfoxides
    作者:Kevin Burgess、Ian Henderson、Kwok Kan Ho
    DOI:10.1021/jo00030a044
    日期:1992.2
    Two methods are presented for kinetic resolutions of compounds containing ester and sulfoxide functionalities (sulfinylalkanoates). In the first a crude lipase preparation from Pseudomonas sp. (K10) mediates enantioselective hydrolysis of these esters in an aqueous environment. The second method uses the same lipase preparation to promote enantioselective transesterifications with alcohols in hexane. Both procedures are suitable for preparation of sulfinylalkanoates where the ester and sulfoxide groups are separated by one or two methylene units (sulfinylacetates and sulfinylpropanoates) but compounds with three methylene "spacer groups" (sulfinylbutanoates) are not substrates for the lipase under either set of conditions.
  • Enzymatic Resolution and Decarboxylative Functionalization of α‐Sulfinyl Esters
    作者:Suraksha Gahalawat、Yesu Addepalli、Stephen P. Fink、Lakshmi Kasturi、Sanford D. Markowitz、Joseph M. Ready
    DOI:10.1002/chem.202302996
    日期:2024.2
    Enzymatic resolution of α-sulfinyl esters gives recovered ester and α-sulfinyl acid in high enantiomeric purity. Decarboxylative functionalization provides access to a wide range of optically active sulfoxides in both enantiomeric forms.
    α-亚爷酯的酶促分离得到具有高对映体纯度的回收酯和 α-亚爷酸。脱羧官能团化提供了两种对映体形式的多种光学活性亚砜。
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