Total synthesis of indole and dihydroindole alkaloids. VI. The total synthesis of some monomeric vinca alkaloids: dl-vincadine, dl-vincaminoreine, dl-vincaminorine, dl-vincadifformine, dl-minovine and dl-vincaminoridine. - Suppr | 超能文献

Total synthesis of indole and dihydroindole alkaloids. VI. The total synthesis of some monomeric vinca alkaloids: dl-vincadine, dl-vincaminoreine, dl-vincaminorine, dl-vincadifformine, dl-minovine and dl-vincaminoridine.

作者信息

Kutney J P, Chan K K, Failli A, Fromson J M, Gletsos C, Leutwiler A, Nelson V R, de Souza J P

出版信息

Helv Chim Acta. 1975 Sep 24;58(6):1648-71. doi: 10.1002/hlca.19750580620.

DOI:10.1002/hlca.19750580620

Abstract

摘要

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

相似文献

1

Total synthesis of indole and dihydroindole alkaloids. VI. The total synthesis of some monomeric vinca alkaloids: dl-vincadine, dl-vincaminoreine, dl-vincaminorine, dl-vincadifformine, dl-minovine and dl-vincaminoridine.

Helv Chim Acta. 1975 Sep 24;58(6):1648-71. doi: 10.1002/hlca.19750580620.

2

The total synthesis of some monomeric Vinca alkaloids: dl-vincadine, dl-vincaminoreine, dl-vincaminorine, dl-vincadifformine, dl-minovine, and dl-vincaminoridine.

J Am Chem Soc. 1968 Jul 3;90(14):3891-3. doi: 10.1021/ja01016a069.

3

Total synthesis of indole and dihydroindole alkaloids. VIII. Studies on the synthesis of bisindole alkaloids in the vinblastine-vincristine series. The chloroindolenine approach.吲哚和二氢吲哚生物碱的全合成。VIII. 长春碱 - 长春新碱系列中双吲哚生物碱合成的研究。氯代吲哚烯方法。

Helv Chim Acta. 1975 Sep 24;58(6):1690-719. doi: 10.1002/hlca.19750580622.

4

New compounds with cytotoxic and antitumor effects. Part 6: Monomeric indole alkaloids of vinca minor L. and their effect on P388 cells.具有细胞毒性和抗肿瘤作用的新型化合物。第6部分：小蔓长春花的单体吲哚生物碱及其对P388细胞的作用。

Pharmazie. 1986 Apr;41(4):270-2.

5

Total synthesis of indole and dihydroindole alkaloids. VII. The total synthesis of isovelbanamine, velbanamine, cleavamine, 18beta-carbomethoxycleavamine and catharanthine.吲哚和二氢吲哚生物碱的全合成。VII. 异长春胺、长春胺、裂胺、18β-甲氧基羰基裂胺和长春花碱的全合成。

Helv Chim Acta. 1975 Sep 24;58(6):1672-89. doi: 10.1002/hlca.19750580621.

6

[Alkaloids from Vinca minor L. Vincadine, minovine and vincorine].[小蔓长春花中的生物碱。长春定碱、米诺碱和长春罗新碱]

Experientia. 1962 Dec 15;18:564-5. doi: 10.1007/BF02172182.

7

General access to the vinca and tacaman alkaloids using a Rh(II)-catalyzed cyclization/cycloaddition cascade.使用铑（II）催化的环化/环加成串联反应实现长春花生物碱和塔卡曼生物碱的通用合成方法。

J Org Chem. 2008 Apr 4;73(7):2792-802. doi: 10.1021/jo8001003. Epub 2008 Mar 5.

8

Studies on the total synthesis of bisindole alkaloids in the vinblastine-vincristine series.

Lloydia. 1977 Jan-Feb;40(1):107-26. doi: 10.1002/chin.197711357.

9

Total synthesis of natural (+)- [corrected] and ent-(-)-4-desacetoxy-6,7-dihydrovindorosine [corrected] and natural and ent-minovine: oxadiazole tandem intramolecular Diels-Alder/1,3-dipolar cycloaddition reaction.天然（+）-[校正后]和对映体（-）-4-去乙酰氧基-6,7-二氢长春罗新碱[校正后]以及天然和对映体米诺碱的全合成：恶二唑串联分子内狄尔斯-阿尔德/1,3-偶极环加成反应

Org Lett. 2005 Feb 17;7(4):741-4. doi: 10.1021/ol050017s.

10

Total synthesis of indole and dihydroindole alkaloids. IV. The total synthesis of dl-dihydrocleavamine, dl-carbomethoxydihydrocleavamine, dl-coronaridine, dl-dihydrocatharanthine, and dl-ibogamine. A general entry into the iboga and vinca alkaloids.吲哚和二氢吲哚生物碱的全合成。IV. dl-二氢裂胺、dl-甲氧基羰基二氢裂胺、dl-冠狗牙花定、dl-二氢长春花碱和dl-伊波加明的全合成。伊波加生物碱和长春花生物碱的通用合成方法。

J Am Chem Soc. 1970 Mar 25;92(6):1712-26. doi: 10.1021/ja00709a051.

引用本文的文献

1

Total synthesis of (-)- and ent-(+)-vindoline and related alkaloids.（-）-和对映-（+）-长春多灵及相关生物碱的全合成。

J Am Chem Soc. 2006 Aug 16;128(32):10596-612. doi: 10.1021/ja061256t.

2

Total synthesis of natural (+)- [corrected] and ent-(-)-4-desacetoxy-6,7-dihydrovindorosine [corrected] and natural and ent-minovine: oxadiazole tandem intramolecular Diels-Alder/1,3-dipolar cycloaddition reaction.天然（+）-[校正后]和对映体（-）-4-去乙酰氧基-6,7-二氢长春罗新碱[校正后]以及天然和对映体米诺碱的全合成：恶二唑串联分子内狄尔斯-阿尔德/1,3-偶极环加成反应

Org Lett. 2005 Feb 17;7(4):741-4. doi: 10.1021/ol050017s.