synthesis and antimicrobial activity of some new quinoxaline derivatives一些新的喹喔啉衍生物的合成及抗菌活性.pdfVIP

synthesis and antimicrobial activity of some new quinoxaline derivatives一些新的喹喔啉衍生物的合成及抗菌活性.pdf

  1. 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
  2. 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载
  3. 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
  4. 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
  5. 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们
  6. 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
  7. 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
synthesis and antimicrobial activity of some new quinoxaline derivatives一些新的喹喔啉衍生物的合成及抗菌活性

Pharmaceuticals 2010, 3, 2416-2425; doi:10.3390/ph3082416 OPEN ACCESS pharmaceuticals ISSN 1424-8247 /journal/pharmaceuticals Article Synthesis and Antimicrobial Activity of Some New Quinoxaline Derivatives Dharmchand Prasad Singh 1,*, Sanjay Kumar Deivedi 1, Syed Riaz Hashim 1 2 and Ram Gopal Singhal 1 Department of Pharmaceutical Chemistry, College of Pharmacy, Institute of Foreign Trade and Management, Moradabad - 244001, India; E-Mails: sanjaydeivedi@yahoo.co.in (S.K.D.); sriaz_hashim@ (S.R.H.) 2 School of Pharmaceutical Sciences, Shobhit University, Meerut, India; E-Mail: drrgsinghal@ (R.G.S.) * Author to whom correspondence should be addressed; E-Mail: dcp_singh@; Tel.: +91-983-708-5047; Fax: +91-591-236-0818. Received: 25 May 2010; in revised form: 13 July 2010 / Accepted: 16 July 2010 / Published: 30 July 2010 Abstract: 2-Chloro-3-methylquinoxaline was selected as a nucleus around which various molecular transformations were performed to obtain new compounds expected to possess optimized antimicrobial activity. As very little work regarding attachment of ether linkages replacing chlorine at C-2 has been reported, it was thought worthwhile to synthesize various quinoxaline derivatives by replacing the C2 chlorine with an ether linkage attached to a benzene ring possessing an aldehyde or a free amino group which can be further reacted with aromatic amines and aromatic aldehydes, respectively, to yield new Schiff bases conta

您可能关注的文档

文档评论(0)

118zhuanqian + 关注
实名认证
文档贡献者

该用户很懒,什么也没介绍

1亿VIP精品文档

相关文档