SYNTHESIS OF 3-ω-EPOXIDO FARNESYL INDOLES, INTERMEDIATES IN THE BIOGENESIS OF SESQUITERPENIC INDOLE ALKALOIDS

DOI: 10.1016/S0040-4039(00)98704-5

Source and publish data:

Tetrahedron Letters p. 3985 - 3988 (1985)

Update date:2022-08-03

Topics:

Authors:

Mirand, Catherine

Maindreville, Michele Doee de

Levy, Jean

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0040-4039(00)98704-5

Epoxides 1a,b, the probable bioprecursors of a serie of indoloterpene alkaloids, were synthesized from indole and farnesyl bromides through application of the Van Tamelen regiospecific epoxidation process to the derived N-acylindolines 14a,b.

Full text of DOI:10.1016/S0040-4039(00)98704-5

Products guided by the article

Product name:1-{3-[(2E,6E)-9-(3,3-Dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-2,3-dihydro-indol-1-yl}-2,2,2-trifluoro-ethanone

Cas No:102720-41-2

R&D Labs maybe for 102720-41-2

XZL BIO-TECHNOLOGY CO., LTD.

Contact:0086 533 2282832

Address:Zibo，Shandong
Jiangsu Cale New Material Co.ltd

Contact:+86-515-88334667/88203550

Address:Zhongshan 3rd Road, Coastal Chemical Industry Park, Yancheng, Jiangsu, China
Jiangxi Global Natural Spice Co., Ltd.

website:https://www.jxhqxl.com/

Contact:+86-796-8106598

Address:No.89, Wenshan Road,South Industrial Park, Jishui County,Jiangxi Province
FUJIAN SHANSHUI CHEMICAL CORP.LTD.

Contact:+86-151-59920036

Address:Jinqiao Gareden, jo@fj-xinyi.com
Beijing Mashi Fine Chemical Co.,Ltd.

Contact:+86-10-61271592

Address:Room 506, Section B, Kaichi Mansion, Industrial Development

Relevant to this article

Doi:10.1021/ja01014a042
(1968)
A methodology for simultaneous fluorogenic derivatization and boronate affinity enrichment of 3-nitrotyrosine-containing peptides

Doi:10.1016/j.ab.2011.07.024
(2011)
Asymmetric synthesis of polyhydroxy α-amino acids with the sulfinimine-mediated asymmetric Strecker reaction: 2-amino 2-deoxy l-xylono-1,5-lactone (polyoxamic acid lactone)

Doi:10.1021/jo020302e
(2002)
Norhierridin B, a new hierridin B-based hydroquinone with improved antiproliferative activity

Doi:10.3390/molecules25071578
(2020)
Synthesis of obscuraminol A using an organocatalyzed enantioselective Henry reaction

Doi:10.1016/j.tet.2016.08.070
(2016)
High temperature ethylene polymerization catalyzed by titanium(iv) complexes with tetradentate aminophenolate ligands in cis-O, N, N chelating mode

Doi:10.1039/c4dt01122h
(2014)

Article Doi