dimethyl(3-phenylprop-2-yn-1-yl)sulfonium bromide | 23451-58-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: dimethyl(3-phenylprop-2-yn-1-yl)sulfonium bromide
• 英文别名: (3-phenylprop-2-yn-1-yl)dimethylsulfonium bromide；dimethyl(3-phenylprop-2-ynyl)sulfonium bromide；Dimethyl-(3-phenylpropin-(2)-yl)-sulfoniumbromid
• CAS: 23451-58-3
• 化学式: Br*C₁₁H₁₃S
• 分子量: 257.194
• InChiKey: BOWRPOPAWLWONG-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  -1.08
• 重原子数：
  13.0
• 可旋转键数：
  1.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  0.0
• 氢给体数：
  0.0
• 氢受体数：
  0.0

反应信息

• 作为反应物：
  描述：

  dimethyl(3-phenylprop-2-yn-1-yl)sulfonium bromide 在 sodium hydride 作用下， 生成 (2-Phenyl-Δ^2,3-butadienyl)-methylsulfid
  参考文献：
  名称：

  Terada,A.; Kishida,Y., Chemical and pharmaceutical bulletin, 1969, vol. 17, p. 966 - 973

  摘要：

  DOI：
• 作为产物：
  描述：

  二甲基硫 、 1-bromo-3-phenylprop-2-yne 以 丙酮 为溶剂， 生成 dimethyl(3-phenylprop-2-yn-1-yl)sulfonium bromide
  参考文献：
  名称：

  通过金催化的乙炔基氮丙啶的环异构化，轻松，区域选择性地合成2,5-二取代的吡咯

  摘要：

  乙炔基氮丙啶的金催化的环异构化反应以高收率提供了2,5-二取代的吡咯。质子物种的存在加快了反应速度并提高了吡咯产物的产率。

  DOI：

  10.1016/j.tetlet.2009.05.091

文献信息

• Regioselective N-Addition/Substitution Reaction of α-Alkylidene Pyrazolinones with Propargyl Sulfonium Salts to Construct Allylthio-Containing Pyrazolones
  作者：Shou-Jie Shen、Xiao-Li Du、Xiao-Li Xu、Ming-Gang Zhao、Jin-Yan Liang

  DOI：10.1021/acs.joc.9b02029

  日期：2019.10.4

  The regioselective N-addition/substitution reaction between α-alkylidene pyrazolinones and propargyl sulfonium salts has been developed to construct functionalized allylthio-containing pyrazolones with moderate to excellent yields. α-Alkylidene pyrazolinones act as N-nucleophilic agents which are distinguished from reported C-nucleophilic reactions. Excellent regioselectivity, readily available starting

  已经开发了α-亚烷基吡唑啉酮类与炔丙基salts盐之间的区域选择性N-加成/取代反应，以中等至优异的产率构建官能化的含烯丙基硫基的吡唑啉酮。α-亚烷基吡唑啉酮类作为N-亲核试剂，与已报道的C-亲核反应不同。出色的区域选择性，易于获得的起始原料，广泛的底物范围，克级合成以及简单的操作，说明了这种新反应途径的合成优势。
• The reaction of prop-2-ynylsulfonium salts and sulfonyl-protected β-amino ketones to epoxide-fused 2-methylenepyrrolidines and S-containing pyrroles
  作者：Tingting Jia、Gongruixue Zeng、Chong Zhang、Linghui Zeng、Wenya Zheng、Siyao Li、Keyi Wu、Jiaan Shao、Jiankang Zhang、Huajian Zhu

  DOI：10.1039/d0cc07745c

  日期：——

  A novel divergent domino annulation reaction of prop-2-ynylsulfonium salts with sulfonyl-protected β-amino ketones has been developed, affording various epoxide-fused 2-methylenepyrrolidines and S-containing pyrroles in moderate to excellent yields. Prop-2-ynylsulfonium salts act as C2 synthons in the reactions providing a promising epoxide-fused skeleton in a single operation with readily accessible

  已经开发了丙-2-炔基salts盐与磺酰基保护的β-氨基酮的新型发散性多米诺环化反应，以中等到极好的收率提供了各种环氧化物稠合的2-亚甲基吡咯烷和含S的吡咯。丙-2-炔基salts盐在反应中充当C 2合成子，可通过易于操作的起始原料在单次操作中提供有希望的环氧融合骨架。
• Isotopic labelling studies for a gold-catalysed skeletal rearrangement of alkynyl aziridines
  作者：Paul W Davies、Nicolas Martin、Neil Spencer

  DOI：10.3762/bjoc.7.96

  日期：——

  Isotopic labelling studies were performed to probe a proposed 1,2-aryl shift in the gold-catalysed cycloisomerisation of alkynyl aziridines into 2,4-disubstituted pyrroles. Two isotopomers of the expected skeletal rearrangement product were identified using (13)C-labelling and led to a revised mechanism featuring two distinct skeletal rearrangements. The mechanistic proposal has been rationalised against

  进行同位素标记研究以探测在金催化的炔基氮丙啶环异构化成 2,4-二取代吡咯中所提出的 1,2-芳基位移。使用 (13) C 标记确定了预期骨骼重排产物的两种同位素，并导致了具有两种不同骨骼重排的修订机制。针对一系列 (13) C 和氘标记底物的反应，该机制建议已被合理化。
• Divergent Domino Reactions of Prop-2-ynylsulfonium Salts: Access to Sulfur-Containing Benzo-Fused Dioxabicyclo[3.3.1]nonanes and Dihydrofuro[2,3-<i>c</i>]chromenes
  作者：Yiming Zhou、Yu Chen、You Huang

  DOI：10.1021/acs.orglett.0c02025

  日期：2020.8.7

  domino annulation reactions between 2-hydroxy-2-methylchromene derivatives and prop-2-ynylsulfonium salts have been developed. Specifically, a sequential [4 + 2] and [4 + 2] annulation reaction occurred in 1,2-dichloroethane affording sulfur-containing benzo-fused dioxabicyclo[3.3.1]nonanes. In contrast, by changing the solvent to toluene, the reaction course switched to a [4 + 2] and [4 + 1] annulation

  已经开发了2-羟基-2-甲基苯甲基衍生物和丙-2-炔基ulf盐之间的溶剂控制的发散性多米诺环化反应。具体地，在[1，2-二氯乙烷]中发生顺序的[4 + 2]和[4 + 2]环化反应，得到含硫的苯并稠合的二氧杂双环[3.3.1]壬烷。相反，通过将溶剂改变为甲苯，反应过程切换为[4 + 2]和[4 +1]环化反应，得到二氢呋喃[2,3- c ]二甲基苯。值得注意的是，丙-2-炔基salt盐首次以其γ-碳原子参与转化。
• A Formal [3+2] Annulation of <i>β</i> ‐Oxoamides and 3‐Alkyl‐ or 3‐Aryl‐Substituted Prop‐2‐Ynyl Sulfonium Salts: Substrate‐Controlled Chemoselective Synthesis of Substituted <i>γ</i> ‐Lactams and Furans
  作者：Bicheng Deng、Chitturi Bhujanga Rao、Rui Zhang、Jiacheng Li、Yongjiu Liang、Yanning Zhao、Ming Gao、Dewen Dong

  DOI：10.1002/adsc.201900693

  日期：2019.10.8

  A substrate‐controlled synthesis of substituted γ‐lactams and furans has been developed via a formal [3+2] annulation of β‐oxoamides and 3‐alkyl/arylprop‐2‐ynyl sulfonium salts in the presence of cesium carbonate in a chemoselective manner. This novel protocol features easily available starting materials, mild reaction conditions, simple execution, and good to excellent yields of products.

  取代的甲基片控制的合成γ β-内酰胺类和呋喃已经开发通过正式[3 + 2]环β在碳酸铯的存在下和-oxoamides 3-烷基/ arylprop -2-炔基锍盐在化学选择性的方式。这种新颖的方案具有容易获得的起始原料，温和的反应条件，简单的实施以及良好至极好的产品收率的特点。