|本期目录/Table of Contents|

[1]周巍,黄翔,巨修练*.3,5二甲基4叔丁基2,6,7双环硫化磷酸酯的合成[J].武汉工程大学学报,2010,(05):28-30.[doi:10.3969/j.issn.16742869.2010.05.008]
 Zhou Wei,Huang Xiang,Ju Xiu Lian*.Synthesis of 3,5dimethyl4tbutylbicyclophosphorothionate[J].Journal of Wuhan Institute of Technology,2010,(05):28-30.[doi:10.3969/j.issn.16742869.2010.05.008]
点击复制

3,5二甲基4叔丁基2,6,7双环硫化磷酸酯的合成(/HTML)
分享到:

《武汉工程大学学报》[ISSN:1674-2869/CN:42-1779/TQ]

卷:
期数:
2010年05期
页码:
28-30
栏目:
化学与化学工程
出版日期:
2010-05-31

文章信息/Info

Title:
Synthesis of 3,5dimethyl4tbutylbicyclophosphorothionate
文章编号:
16742869(2010)05002803
作者:
周巍 黄翔巨修练*
武汉工程大学化工与制药学院,湖北省新型反应器与绿色化学工艺重点实验室, 湖北 武汉 430074
Author(s):
Zhou Wei Huang Xiang Ju XiuLian*
Hubei Key Laboratory of Novel Chemical Reactor and Green Chemical Technology, School of Chemical Engineering
and Pharmacy, Wuhan Institute of Technology, Wuhan 430074,China
关键词:
GABA受体双环硫化磷酸酯合成杀虫剂
Keywords:
GABA receptorbicyclophosphorothionatesynthesisinsecticide
分类号:
O626.23
DOI:
10.3969/j.issn.16742869.2010.05.008
文献标志码:
A
摘要:
以乙酰丙酮为起始原料,经烷基化,羟甲基化,还原,最后与PSCl3环合,成功合成了1硫代1磷杂3,5二甲基4叔丁基2,6,7三氧杂双环[2,2,2]辛烷.目标化合物及部分中间体的结构均通过1H NMR、MS进行了结构确证.
Abstract:
Bicyclophosphorothionates are GABA receptor antagonists which show the selectivity between insects and mammals. 1 sulfo1 phosphor3, 5dimethyl4tbutyl2,6,7trioxabicyclo [2,2,2]octane was synthesized from acetylacetone via alkylation, hydroxymethylation, reduction and cyclization with PSCl3. The target compound is confirmed by 1H NMR,MS spectra.

参考文献/References:

[1]Okada Y,NitschHassler C,Kim J S,et a1.Role of γaminobutyricacid(GABA)in the Extrapyramidal Motor System l Regional Distribution of GABA in Rabbit,Rat,Guinea Pig,and Baboon CNS [J].Exp Brain Res,1971,13:514518.
[2]巨修练.GABAA受体及其非竞争性拮抗剂的研究进展望[J].世界农药,2007,29(1):2833.
[3]Squires R F, Casida J E, Rechardson M etal,Rechardson Meta1.[35S]tbutylbicyclophosphorothionate Binds with High Affinity to Brain Specific Sites Coupled to γAminobutyric AcidA and Ion Recognition Sites [J].Mol Pharmaco1,1983,23:326336.
[4] Ju X L,Ozoe Y.Bicyclophosphorothionate Antagonists Exhibiting Selectivity for Housefly GABA Receptors [J]. Pestic Sci,1999,55:971982.
[5]Kuriyama T,Ju X L,Ozoe Y,et a1.Nematocidal Quassinoids andBicyclophosphorothianates:A Possible Common Mode of Action on the GABA receptor [J].Pestic Biochem Physio1,2005,81:176187.
[6]Ozoe Y,Akamatsa M,Higata T,et a1.Picrodendrin and Related Terpenoid Antagonists Reveal Structural Differences between lonotropic GABA Receptors of Mammals and Insects.Bioorg Med Chem,1998(6):481492.
[7]吴有斌,周巍,巨修炼.4烃基3氰基双环笼状磷酸酯类化合物的合成及生物活性研究[J].有机化学,2008,28(7):12731277.
[8]Jens C,Thomas K,Thomas W, et al.Cerium  Catalyzed αHydroxylation Reactions of αCyclopropyl βDicarbonyl Compounds with Molecular Oxygen [J]. Eur.J Org Chem,2006:26012608.
[9]Yoshihisa O,Morifusa E. Synthesis and Some Spectral Characteristics of Bicyclic Phosphate,GABA Antagonists[J].Agric Biol Chem,1982,46(2):411418.
[10]王恩思,张广良,金磊.新型抗病毒药物法昔洛韦的合成[J].吉林大学自然科学学报,2000,1(1):9598.
[11]Soai K,Oyamada H,Okawa A.Sodium Borohydridetbutyl AlcoholMethanol as An Efficent System for the Selective Reduction of Esters [J]. Synth Commun,1982,12(6):463467.
[12]刑其毅,裴伟伟,徐瑞秋,等.基础有机化学:下册[M].3版.北京:高等教育出版社:654659.

相似文献/References:

[1]黄翔,黄强,周巍,等.1-(4′-乙炔基苯基)-4-正丙基-2,6,7-三氧杂双环[2.2.2]辛烷的合成[J].武汉工程大学学报,2011,(05):15.[doi:10.3969/j.issn.16742869.2011.05.005]
 HUANG Xiang,HUANG Qiang,ZHOU Wei,et al.Synthesis of 1-(4′-ethynylphenyl)-4-n-propyl-2,6,7-trioxabicyclo[2.2.2]octane[J].Journal of Wuhan Institute of Technology,2011,(05):15.[doi:10.3969/j.issn.16742869.2011.05.005]
[2]陈佳丽,等.亚氨基哒嗪类衍生物对人与昆虫GABA受体的选择性研究[J].武汉工程大学学报,2019,(01):12.[doi:10. 3969/j. issn. 1674?2869. 2019. 01. 002]
 CHEN Jiali,ZHAI Na,CHEN Da,et al.Selectivity of Iminopyridazine Derivatives for GABA Receptors in Human Being and Insects[J].Journal of Wuhan Institute of Technology,2019,(05):12.[doi:10. 3969/j. issn. 1674?2869. 2019. 01. 002]

备注/Memo

备注/Memo:
收稿日期:20100320基金项目:国家自然科学基金(No.20572084)作者简介:周巍(1984),男,湖北武汉人,硕士研究生.研究方向:药物合成.指导老师:巨修练,教授,博士.研究方向:新农药研发,生物活性测试,计算机药物辅助设计.
更新日期/Last Update: