• 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

Novel analgesics and molecular rearrangements in the morphine-thebaine group. VI. Base-catalyzed rearrangements in the 6,14-endo-ethenotetrahydrothebaine series.

作者信息

Bentley K W, Hardy D G, Crocker H P, Haddlesey D I, Mayor P A

出版信息

J Am Chem Soc. 1967 Jun 21;89(13):3312-21. doi: 10.1021/ja00989a035.

DOI:10.1021/ja00989a035
PMID:6042767
Abstract
摘要

相似文献

1
Novel analgesics and molecular rearrangements in the morphine-thebaine group. VI. Base-catalyzed rearrangements in the 6,14-endo-ethenotetrahydrothebaine series.
J Am Chem Soc. 1967 Jun 21;89(13):3312-21. doi: 10.1021/ja00989a035.
2
Novel analgesics and molecular rearrangements in the morphine-thebaine group. IV. Acid-catalyzed rearrangements of alcohols of the 6,14-endo-ethenotetrahydrothebaine series.吗啡-蒂巴因类中的新型镇痛药及分子重排。IV. 6,14-内-乙烯基四氢蒂巴因系列醇的酸催化重排
J Am Chem Soc. 1967 Jun 21;89(13):3293-303. doi: 10.1021/ja00989a033.
3
Novel analgesics and molecular rearrangements in the morphine--thebaine group. XII. Derivatives of 7-amino-6,14-endo-ethenotetrahydrothebaine.
J Chem Soc Perkin 1. 1969;17:2235-6.
4
Novel analgesics and molecular rearrangements in the morphine-thebaine group. II. Alcohols derived from 6,14-endo-etheno- and 6,14-endo-ethanotetrahydrothebaine.
J Am Chem Soc. 1967 Jun 21;89(13):3273-80. doi: 10.1021/ja00989a031.
5
Novel analgesics and molecular rearrangements in the morphine-thebaine group. V. Derivatives of 7,8-dihydrocyclohexeno[1',2':8,14]codeinone.
J Am Chem Soc. 1967 Jun 21;89(13):3303-11. doi: 10.1021/ja00989a034.
6
Novel analgesics and molecular rearrangements in the morphine-thebaine group. XXV. Substitution of the piperidine ring in derivatives of 6,14-endo-ethenotetrahydrothebaine.
J Chem Soc Perkin 1. 1972;6:875-8. doi: 10.1039/p19720000875.
7
Novel analgesics and molecular rearrangements in the morphine-thebaine group. 3. Alcohols of the 6,14-endo-ethenotetrahydrooripavine series and derived analogs of N-allylnormorphine and -norcodeine.
J Am Chem Soc. 1967 Jun 21;89(13):3281-92. doi: 10.1021/ja00989a032.
8
Novel analgesics and molecular rearrangements in the morphine-thebaine group. XIV. Substitution in the aromatic nucleus in derivatives of 6,14-endo-ethenotetrahydrothebaine.
J Chem Soc Perkin 1. 1969;17:2241-2. doi: 10.1039/j39690002241.
9
Novel analgetics and molecular rearrangements in the morphine-thebaine group. 29. Aryl and arylalkyl tertiary alcohols in the 6,14-endo-ethenotetrahydrothebaine series.吗啡-蒂巴因类中的新型镇痛药与分子重排。29. 6,14-内乙烯基四氢蒂巴因系列中的芳基和芳基烷基叔醇。
J Med Chem. 1973 Jan;16(1):84-5. doi: 10.1021/jm00259a024.
10
Novel analgesics and molecular rearrangements in the morphine-thebaine group. 8. 7-Alkyl-6,14-endo-ethenotetrahydro-thebaine and related compounds.
J Chem Soc Perkin 1. 1969;5:826-30.

引用本文的文献

1
Diels-Alder Adducts of Morphinan-6,8-Dienes and Their Transformations.吗啡喃-6,8-二烯的 Diels-Alder 加合物及其转化。
Molecules. 2022 Apr 30;27(9):2863. doi: 10.3390/molecules27092863.
2
Nitroso Diels-Alder (NDA) reaction as an efficient tool for the functionalization of diene-containing natural products.亚硝基狄尔斯-阿尔德(NDA)反应作为一种用于含二烯天然产物功能化的有效工具。
Org Biomol Chem. 2014 Oct 14;12(38):7445-68. doi: 10.1039/c4ob01033g.
3
Structural determinants of opioid and NOP receptor activity in derivatives of buprenorphine.
阿片类和 NOP 受体活性在丁丙诺啡衍生物中的结构决定因素。
J Med Chem. 2011 Oct 13;54(19):6531-7. doi: 10.1021/jm2003238. Epub 2011 Sep 7.
4
Microbiological transformation of 6,14-endo-ethenotetrahydrothebaine alkaloids.
Experientia. 1968 Feb 15;24(2):133-4. doi: 10.1007/BF02146941.
5
Analgesic and other actions of morphine antagonists.吗啡拮抗剂的镇痛及其他作用。
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1968;259(2):154-5. doi: 10.1007/BF00537748.