TOTAL SYNTHESIS OF (+/-)-ATRACTYLON AND (+/-)-LINDESTRENE

DOI: 10.1016/S0040-4039(01)84607-4

Source and publish data:

Tetrahedron Letters p. 6393 - 6396 (1985)

Update date:2022-08-06

Topics:: Authors:

Honan, Matthew C.

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

Article abstract of DOI:10.1016/S0040-4039(01)84607-4

The total synthesis of the eudesmane furanosesquiterpenes (+/-)-atractylon (1) and (+/-)-lindestrene (2) is described.Both 1 and 2 were synthesized via the methyl xanthate intermediate (10).

Full text of DOI:10.1016/S0040-4039(01)84607-4

Products guided by the article

Product name:(+/-)-lindestrene

Cas No:16836-53-6

R&D Labs maybe for 16836-53-6

Chengdu King-tiger Pharm-chem. Tech. Co., Ltd

Contact:028-85317716

Address:Tianfu Life Science Park, No. 88 South Keyuan Road, Gaoxin District, Chengdu City, Sichuan Province, PRC.
Ningbo Huajia Chemicals

Contact:+86-574-87065746

Address:10th Floor, No.787 Baizhang East Road,
Xi'an yuanfar international trade company

website:https://www.yuanfarchemical.com

Contact:86-029-88745613 ext 828

Address:Floor19th ,B Building, Oak Block,No.36 South Fenghui Road, Dev. Zone of High-Tech Ind.,Xi’an, China
shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China
Jinan Jiaquan Chemical Co.,Ltd

Contact:+86-531-62318366

Address:Room 502 of Yidonghuayuan No.601 Huaxin Road Licheng District Jinan China

Relevant to this article

Synthesis of endolides A and B: Naturally occurring N-methylated cyclic tetrapeptides

Doi:10.1039/c9md00050j
(2019)
Synthesis of tris(cyclohexylisocyanide)bis(triphenylphosphine)cobalt(II) perchlorate. An example of unusual stabilization of the cobalt(II) oxidation state

Doi:10.1080/00945719708003157
(1997)
Gadolinium complex of tris[(3-hydroxy-1-methyl-2-oxo-1,2-didehydropyridine-4-carboxamido)eth yl]-amine: A new class of gadolinium magnetic resonance relaxation agents

Doi:10.1021/ja00132a025
(1995)
N-Heterocyclic Carbene/Cobalt Cooperative Catalysis for the Chemo- and Regioselective C?N Bond Formation between Aldehyde and Amines/Amides

Doi:10.1002/cctc.202000156
(2020)
Acyliminothiadiazoline derivatives: New, highly potent, and orally active angiotensin II receptor antagonists

Doi:10.1016/S0960-894X(96)00250-8
(1996)
Synthesis, toxicological, pharmacological, and bronchodilating activity in vitro of some xanthineacetic acid derivatives

Doi:10.1002/ardp.19953280709
(1995)

Article Doi

TOTAL SYNTHESIS OF (+/-)-ATRACTYLON AND (+/-)-LINDESTRENE

DOI: 10.1016/S0040-4039(01)84607-4

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(01)84607-4

Full text of DOI:10.1016/S0040-4039(01)84607-4

Products guided by the article

R&D Labs maybe for 16836-53-6

Relevant to this article

Hot Product