• 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

对映体纯的1-芳基丙-2-烯-1-醇及其叔丁基碳酸酯的合成。

Synthesis of enantiopure 1-arylprop-2-en-1-ols and their tert-butyl carbonates.

作者信息

Stambaský Jan, Malkov Andrei V, Kocovský Pavel

机构信息

Department of Chemistry, WestChem, University of Glasgow, Glasgow G12 8QQ, Scotland, UK.

出版信息

J Org Chem. 2008 Nov 21;73(22):9148-50. doi: 10.1021/jo801874r. Epub 2008 Oct 8.

DOI:10.1021/jo801874r
PMID:18839990
Abstract

Enantiomerically pure 1-arylpropenols 8 have been prepared by resolution of the corresponding racemates, using the lipase formulation Novozyme 435. Deprotonation of the latter alcohols with n-BuLi, followed by derivatization with (t-BuO)2CO, afforded the corresponding carbonates 5. Optimization of the process is presented.

摘要

通过使用脂肪酶制剂诺维信435拆分相应的外消旋体,制备了对映体纯的1-芳基丙烯醇8。用正丁基锂使后一种醇去质子化,然后用二叔丁基碳酸酯进行衍生化,得到了相应的碳酸酯5。本文介绍了该工艺的优化。

相似文献

1
Synthesis of enantiopure 1-arylprop-2-en-1-ols and their tert-butyl carbonates.对映体纯的1-芳基丙-2-烯-1-醇及其叔丁基碳酸酯的合成。
J Org Chem. 2008 Nov 21;73(22):9148-50. doi: 10.1021/jo801874r. Epub 2008 Oct 8.
2
An efficient CuCN-catalyzed synthesis of optically active 2,3-allenols from optically active 1-substituted 4-chloro-2-butyn-1-ols.一种由光学活性的1-取代-4-氯-2-丁炔-1-醇通过氰化亚铜催化高效合成光学活性2,3-丙二烯醇的方法。
J Org Chem. 2009 Jul 17;74(14):5104-6. doi: 10.1021/jo900710e.
3
Synthesis of enantiomerically pure cyclohex-2-en-1-ols: development of novel multicomponent reactions.对映体纯环己-2-烯-1-醇的合成:新型多组分反应的开发
Chemistry. 2005 Jul 4;11(14):4210-8. doi: 10.1002/chem.200401258.
4
Influence of HMPA on the stereochemical outcome of the addition of a racemic allenylzinc onto enantiopure N-tert-butanesulfinimines: stereoselective access to enantiopure cis-ethynylaziridines.
Chemistry. 2005 Sep 5;11(18):5269-78. doi: 10.1002/chem.200500268.
5
Utilization of N-X bonds in the synthesis of N-heterocycles.N-X键在氮杂环合成中的应用。
Acc Chem Res. 2009 Aug 18;42(8):1172-82. doi: 10.1021/ar900059r.
6
Synthesis of enantiopure tert-butanesulfinamide from tert-butanesulfinyloxazolidinone.
J Org Chem. 2004 Nov 26;69(24):8533-6. doi: 10.1021/jo048576k.
7
Chemoenzymatic synthesis of rivastigmine based on lipase-catalyzed processes.基于脂肪酶催化过程的卡巴拉汀化学酶法合成。
J Org Chem. 2009 Aug 7;74(15):5304-10. doi: 10.1021/jo900784g.
8
Arthrobacter sp. lipase immobilization for preparation of enantiopure masked beta-amino alcohols.用于制备对映体纯的掩蔽β-氨基醇的节杆菌属脂肪酶固定化
Bioorg Med Chem. 2009 Jan 1;17(1):29-34. doi: 10.1016/j.bmc.2008.11.023. Epub 2008 Nov 18.
9
A flexible route to chiral 2-endo-substituted 9-oxabispidines and their application in the enantioselective oxidation of secondary alcohols.
J Org Chem. 2009 Feb 6;74(3):1407-10. doi: 10.1021/jo802409x.
10
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.新型N-亚磺酰基-N'-叔丁基-N,N'-二酰肼的合成及其杀虫活性。3. N-(烷基二硫代)、N-(氨基硫代)和N,N-二硫代衍生物
J Agric Food Chem. 2008 Nov 26;56(22):10799-804. doi: 10.1021/jf802389r.

引用本文的文献

1
Iterative synthesis of stereodefined polyacetals and their domino-Coates-Claisen rearrangement.立体定向聚缩醛的迭代合成及其多米诺-科茨-克莱森重排反应。
Chem Sci. 2025 Jan 24;16(9):3946-3952. doi: 10.1039/d4sc08790a. eCollection 2025 Feb 26.
2
Enhanced catalytic activity and thermal stability of lipase bound to oxide nanosheets.与氧化物纳米片结合的脂肪酶的催化活性和热稳定性增强。
RSC Adv. 2018 Jun 4;8(36):20347-20352. doi: 10.1039/c8ra03558j. eCollection 2018 May 30.
3
Recent strategies and tactics for the enantioselective total syntheses of cyclolignan natural products.
近期手性全合成环木脂素天然产物的策略和战术。
Nat Prod Rep. 2022 Mar 23;39(3):670-702. doi: 10.1039/d1np00057h.
4
Homologated amino acids with three vicinal fluorines positioned along the backbone: development of a stereoselective synthesis.沿主链带有三个相邻氟原子的同源氨基酸:立体选择性合成方法的开发
Beilstein J Org Chem. 2017 Nov 1;13:2316-2325. doi: 10.3762/bjoc.13.228. eCollection 2017.
5
Concise Total Synthesis of Lundurines A-C Enabled by Gold Catalysis and a Homodienyl Retro-Ene/Ene Isomerization.金催化及同二烯基逆烯反应/烯反应异构化实现伦杜林A-C的简洁全合成
J Am Chem Soc. 2016 Mar 23;138(11):3671-4. doi: 10.1021/jacs.6b01428. Epub 2016 Mar 15.