• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

α-杂原子酮在与β-反式硝基烯烃的不对称迈克尔反应中的开发与应用

Development and Application of α-Heteroatom Ketones in Asymmetric Michael Reaction with β-trans-Nitroalkenes.

作者信息

Yang Dongxu, Li Dan, Wang Linqing, Zhao Depeng, Wang Rui

机构信息

†Key Laboratory of Preclinical Study for New Drugs of Gansu Province, Lanzhou University, Lanzhou 730000, People's Republic of China.

§Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China.

出版信息

J Org Chem. 2015 May 1;80(9):4336-48. doi: 10.1021/acs.joc.5b00013. Epub 2015 Apr 22.

DOI:10.1021/acs.joc.5b00013
PMID:25853329
Abstract

The successful design and application of a new type of N-phenyl-imidazole-modified α-heteroatom ketones in asymmetric anti-selective Michael reactions with β-trans-nitroalkenes is reported. High yields and enantioselectivities could be obtained, and the corresponding conjugate adducts could be further transformed into related chiral esters and cyclopropane derivatives with excellent enantioselectivities.

摘要

报道了一种新型N-苯基咪唑修饰的α-杂原子酮在与β-反式硝基烯烃的不对称反选择性迈克尔反应中的成功设计与应用。可以获得高产率和对映选择性,并且相应的共轭加合物可以进一步转化为具有优异对映选择性的相关手性酯和环丙烷衍生物。

相似文献

1
Development and Application of α-Heteroatom Ketones in Asymmetric Michael Reaction with β-trans-Nitroalkenes.α-杂原子酮在与β-反式硝基烯烃的不对称迈克尔反应中的开发与应用
J Org Chem. 2015 May 1;80(9):4336-48. doi: 10.1021/acs.joc.5b00013. Epub 2015 Apr 22.
2
Asymmetric anti-selective Michael reaction of imidazole-modified ketones with trans-β-nitroalkenes.咪唑修饰的酮与反式-β-硝基烯烃的不对称反选择性迈克尔反应。
Chemistry. 2015 Jan 19;21(4):1458-62. doi: 10.1002/chem.201405847. Epub 2014 Nov 28.
3
Asymmetric Michael addition of ketones to nitroolefins: pyrrolidinyl-oxazole-carboxamides as new efficient organocatalysts.酮对硝基烯烃的不对称迈克尔加成反应:吡咯烷基-恶唑-羧酰胺作为新型高效有机催化剂
Org Biomol Chem. 2014 Oct 28;12(40):8008-18. doi: 10.1039/c4ob01223b.
4
Densely Substituted L-Proline Esters as Catalysts for Asymmetric Michael Additions of Ketones to Nitroalkenes.密集取代的L-脯氨酸酯作为酮与硝基烯烃不对称迈克尔加成反应的催化剂。
J Org Chem. 2015 Jun 5;80(11):5588-99. doi: 10.1021/acs.joc.5b00495. Epub 2015 May 27.
5
Pyrrolidinyl-camphor derivatives as a new class of organocatalyst for direct asymmetric Michael addition of aldehydes and ketones to beta-nitroalkenes.吡咯烷基莰醇衍生物作为一类新型有机催化剂,用于醛酮与β-硝基烯烃的直接不对称迈克尔加成反应。
Chemistry. 2010 Jun 18;16(23):7030-8. doi: 10.1002/chem.201000483.
6
Asymmetric Michael/cyclization tandem reaction of 4-hydroxycoumarin with β-nitroalkenes catalyzed by chiral bifunctional thioureas.手性双功能硫脲催化 4-羟基香豆素与β-硝基烯烃的不对称 Michael/环化串联反应。
Org Biomol Chem. 2013 Feb 28;11(8):1286-9. doi: 10.1039/c2ob27121d.
7
Asymmetric Michael addition of α-fluoro-α-nitro esters to nitroolefins: towards synthesis of α-fluoro-α-substituted amino acids.不对称迈克尔加成法 α-氟-α-硝基酯到硝基亚油酸:合成 α-氟-α-取代氨基酸。
Org Biomol Chem. 2015 Feb 28;13(8):2350-9. doi: 10.1039/c4ob02486a.
8
Chiral amine-thioureas bearing multiple hydrogen bonding donors: highly efficient organocatalysts for asymmetric Michael addition of acetylacetone to nitroolefins.带有多个氢键供体的手性胺-硫脲:乙酰丙酮对硝基烯烃不对称迈克尔加成反应的高效有机催化剂。
Chem Commun (Camb). 2008 Mar 28(12):1431-3. doi: 10.1039/b718949d. Epub 2008 Jan 23.
9
Enantioselective conjugate addition of ketones to nitroalkenes catalyzed by pyrrolidine-sulfamides.手性吡咯烷磺酰胺催化的酮对硝基烯烃的对映选择性共轭加成。
Chirality. 2012 Mar;24(3):232-8. doi: 10.1002/chir.21987. Epub 2012 Jan 25.
10
Diastereo- and enantioselective conjugate addition of alpha-ketoesters to nitroalkenes catalyzed by a chiral Ni(OAc)(2) complex under mild conditions.手性 Ni(OAc)2 配合物催化条件下α-酮酯对硝基烯烃的非对映和对映选择性共轭加成反应。
J Am Chem Soc. 2010 Mar 31;132(12):4036-7. doi: 10.1021/ja909457b.

引用本文的文献

1
Nitrocyclopropanes as Valuable Building Blocks in Organic Synthesis and Biology: Exploring the Origin of the Nitro Group.作为有机合成和生物学中重要基石的硝基环丙烷:探索硝基的起源
Chemistry. 2025 Apr 4;31(20):e202404791. doi: 10.1002/chem.202404791. Epub 2025 Feb 10.
2
Crystal structure of N-[(1S,2S)-2-amino-cyclo-hex-yl]-2,4,6-tri-methyl-benzene-sulfonamide.N-[(1S,2S)-2-氨基-环己基]-2,4,6-三甲基-苯磺酰胺的晶体结构
Acta Crystallogr E Crystallogr Commun. 2015 Nov 21;71(Pt 12):1521-4. doi: 10.1107/S205698901502191X. eCollection 2015 Dec 1.