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立体选择性合成2-(a-噻吩甲酰基)-3-取代苯基-4-乙氧羰基-5-甲基-反式-2,3-二氢呋喃
引用本文:姜海燕 曹卫国 张慧 孙汝淑 陈杰 邓红梅 邵敏 朱士正. 立体选择性合成2-(a-噻吩甲酰基)-3-取代苯基-4-乙氧羰基-5-甲基-反式-2,3-二氢呋喃[J]. 中国化学, 2008, 26(4): 736-740. DOI: 10.1002/cjoc.200890137
作者姓名:姜海燕 曹卫国 张慧 孙汝淑 陈杰 邓红梅 邵敏 朱士正
作者单位:上海大学化学系, 上海 200444, 中国 中国科学院上海有机化学研究所金属有机国家重点实验室, 上海 200032, 中国 上海大学分析测试中心上海 200444,中国 中国科学院上海有机化学研究所氟化学开放实验室, 上海 200032, 中国
摘    要:溴化(a-噻吩甲酰基)甲基三苯鉮1与3-取代苯甲叉基-2,4-戊二酮 2以碳酸钾为碱,在苯中55℃条件下反应,可以较好的收率、高立体选择性地生成反-2-(a-噻吩甲酰基)-3-取代苯基-4-乙氧羰基-5-甲基-2,3-二氢呋喃3。产物结构均经波谱予以确定。本文还提出了生成产物的可能机理。

关 键 词:立体选择性合成   胂叶立德   二氢呋呋喃衍生物
收稿时间:2007-06-05
修稿时间:2007-10-08

Stereoselective Synthesis of trans‐2‐Thien‐α‐oyl‐3‐ [(un)substituted phenyl]‐4‐acetyl‐5‐methyl‐2,3‐dihydrofurans
Hai‐Yan JIANG,Wei‐Guo CAO,Hui ZHANG,Ru‐Shu SUN,Jie CHEN,Hong‐Mei DENG,Min SHAO,Shi‐Zheng ZHU. Stereoselective Synthesis of trans‐2‐Thien‐α‐oyl‐3‐ [(un)substituted phenyl]‐4‐acetyl‐5‐methyl‐2,3‐dihydrofurans[J]. Chinese Journal of Chemistry, 2008, 26(4): 736-740. DOI: 10.1002/cjoc.200890137
Authors:Hai‐Yan JIANG  Wei‐Guo CAO  Hui ZHANG  Ru‐Shu SUN  Jie CHEN  Hong‐Mei DENG  Min SHAO  Shi‐Zheng ZHU
Affiliation:1. Department of Chemistry, Shanghai University, Shanghai 200444, China;2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China;3. Instrumental Analysis and Research Center, Shanghai University, Shanghai 200444, China
Abstract:Trans‐2‐thien‐α‐oyl‐3‐[(un)substituted phenyl]‐4‐acetyl‐5‐methyl‐2,3‐dihydrofurans 3 were prepared in good yields with high stereoselectivity by the reaction of thien‐α‐oylmethyltriphenylarsonium bromide 1 with 3‐[(un)substituted benzylidene]‐2,4‐pentadione 2 in benzene in the presence of potassium carbonate at 55 °C. The structure of compound 3 was confirmed by IR, MS, 1H NMR, 1H‐1H COSY, microanalysis and single crystal X‐ray diffraction analysis. The possible reaction mechanism for the formation of products was also proposed.
Keywords:stereoselective synthesis  arsonium ylide  dihydrofuran derivative
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