Stereoselective Synthesis of trans-2-thien-alpha-oyl-3-[(un)substituted phenyl]-4-acetyl-5-methyl-2,3-dihydrofurans
文献类型：期刊论文
| 作者 | Jiang HY(姜海燕) ; Cao WG(曹卫国) ; Zhang H(张慧) ; Sun RS(孙汝淑) ; Chen J(陈杰) ; Deng HM(邓红梅) ; Shao M(邵敏) ; Zhu SZ(朱仕正) |
| 刊名 | Chin. J. Chem.
 |
| 出版日期 | 2008 |
| 卷号 | 26期号:4页码:736-740 |
| ISSN号 | 1001-604X |
| 其他题名 | Stereoselective Synthesis of trans-2-thien-alpha-oyl-3-[(un)substituted phenyl]-4-acetyl-5-methyl-2,3-dihydrofurans |
| 通讯作者 | 曹卫国 ; 朱仕正 |
| 英文摘要 | Trans-2-thien-alpha-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-alpha-oylmethyltriphenylarsonium bromide 1 with 3-[(un)substituted benzylidene]-2,4-pentadione 2 in benzene in the presence of potassium carbonate at 55 degrees C. The structure of compound 3 was confirmed by IR, MS, H-1 NMR, H-1-H-1 COSY, microanalysis and single crystal X-ray diffraction analysis. The possible reaction mechanism for the formation of products was also proposed. |
| 学科主题 | 有机化学 |
| 收录类别 | SCI |
| 原文出处 | http://dx.doi.org/10.1002/cjoc.200890137 |
| 语种 | 英语 |
| WOS记录号 | WOS:000255532800027 |
| 公开日期 | 2013-01-18 |
| 源URL | [http://202.127.28.38/handle/331003/14450]  |
| 专题 | 上海有机化学研究所_中科院有机氟化学重点实验室 |
| 推荐引用方式 GB/T 7714 | Jiang HY,Cao WG,Zhang H,et al. Stereoselective Synthesis of trans-2-thien-alpha-oyl-3-[(un)substituted phenyl]-4-acetyl-5-methyl-2,3-dihydrofurans[J]. Chin. J. Chem.,2008,26(4):736-740. |
| APA | 姜海燕.,曹卫国.,张慧.,孙汝淑.,陈杰.,...&朱仕正.(2008).Stereoselective Synthesis of trans-2-thien-alpha-oyl-3-[(un)substituted phenyl]-4-acetyl-5-methyl-2,3-dihydrofurans.Chin. J. Chem.,26(4),736-740. |
| MLA | 姜海燕,et al."Stereoselective Synthesis of trans-2-thien-alpha-oyl-3-[(un)substituted phenyl]-4-acetyl-5-methyl-2,3-dihydrofurans".Chin. J. Chem. 26.4(2008):736-740. |
入库方式： OAI收割
来源：上海有机化学研究所
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