Formal synthesis of brefeldin A from (+)-limonen-10-ol

DOI: 10.1248/cpb.33.4021

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 4021 - 4025 (1985)

Update date:2022-08-04

Topics:

Authors:

Ueno Ueno

Suemune Suemune

Saeki Saeki

Sakai Sakai

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

Article abstract of DOI:10.1248/cpb.33.4021

Full text of DOI:10.1248/cpb.33.4021

NII-Electronic Library Service

Products guided by the article

Product name:(1S,3S,4R)-1-benzyloxy-3-methoxycarbonyl-4-(3-oxobutyl)-cyclopentane

Cas No:101909-78-8

R&D Labs maybe for 101909-78-8

Chemtrade International ( China )

Contact:+86-532-86893005

Address:Rm 2-501, Huaxia Zonghe Building, No. 410 JInggangshan Road, Huangdao
Zhejiang Sucon Silicone Co.,Ltd

Contact:+86-575-88046692

Address:Qisheng Rd., Paojiang Industrial Zone, Shaoxing, Zhejiang, China.
Jiangsu Zenji Pharmaceuticals LTD

Contact:+86-025-83172562; +1-224-888-1133(USA)

Address:No.5 Xinmofan Road
Kono Chem Co.,Ltd

website:http://www.konochem.com

Contact:86-29-86107037

Address:No.170 West Avenue,Xi’an 710082,China
JADECHEM NINGBO CO.,LTD.

Contact:+86-574-89075960

Address:#100 Xiang Yun Road, New High tech area, Ningbo, China

Relevant to this article

Tandem Rh(I)-catalyzed [(5+2)+1] cycloaddition/aldol reaction for the construction of linear triquinane skeleton: Total syntheses of (±)-hirsutene and (±)-1-desoxyhypnophilin

Doi:10.1021/ja7100449
(2008)
Selective, high affinity A_2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines

Doi:10.1016/j.bmcl.2008.01.008
(2008)
A convenient one-pot synthesis of: N -substituted amidoximes and their application toward 1,2,4-oxadiazol-5-ones

Doi:10.1039/c8ra08207c
(2018)
Doi:10.1021/jo01360a011
(1957)
Facile microwave assisted decarbonylation of 4-formyl group in 5-alkyl amino substituted pyrazoles

Doi:10.1016/j.tetlet.2008.02.020
(2008)
Synthesis of pyrido[2,3-e]pyrrolo[1,2-a]pyrazine derivatives via tandem iminium cyclization and smiles rearrangement

Doi:10.1021/jo702754r
(2008)

Article Doi