Total synthesis of (±)-poitediol and (±)-4-epipoitediol

DOI: 10.1021/ja00325a032

Source and publish data:

Journal of the American Chemical Society p. 3869 - 3870 (1984)

Update date:2022-08-03

Topics:

Authors:

Gadwood Gadwood

Lett Lett

Wissinger

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

Article abstract of DOI:10.1021/ja00325a032

Full text of DOI:10.1021/ja00325a032

Products guided by the article

Product name:2-methoxy-4-methyl-2-cyclohexen-1-ol

Cas No:104070-35-1

R&D Labs maybe for 104070-35-1

Hangzhou Taiyan Trading Co., Ltd(expird)

Contact:+86-13777583958

Address:NO.63, Xingyi Street, Xihu District, Hangzhou, Zhejiang, China
Brichem ( Haikou ) Co. Ltd.

Contact:86-898-65311214

Address:Room 102, BLDG. 68 Jiangnan City, No. 66 Heping Road,Haikou, Hainan, China
Shanghai Korey Pharm Co.,Ltd.(expird)

Contact:021-61840961 021-61840962

Address:No.157,Zhuguang Rd, Qingpu, Shanghai, China
WUHU HUAHAI BIOLOGY ENGINEERING CO LTD

Contact:+86-553-3836920

Address:7/F NO.82 LAODONG ROAD WUHU CHINA
WEIFANG DERUN CHEMICAL CO.,LTD

Contact:86-536-8956886

Address:weifang

Relevant to this article

VALENZISOMERISIERUNGEN DER 7,8-BIS(PHOSPHANO)CYCLOOCTA-1,3,5-TRIENE

Doi:10.1016/S0040-4039(00)95016-0
(1985)
A chiral rhodium carboxamidate catalyst for enantioselective C-H amination

Doi:10.1021/ja8031955
(2008)
4-<2--2-oxoethyl>-8-(phenylmethoxy)-2-naphthalenecarboxylic Acid: A High Affinity, Competitive, Orally Active Leukotriene B₄ Receptor Antagonist

Doi:10.1021/jm00100a034
(1992)
Catalytic Asymmetric Total Synthesis of Macrocyclic Marine Natural Product (–)-Haliclonin A^?

Doi:10.1002/cjoc.202000291
(2020)
Preparation of a chiral synthon for an HBV inhibitor: Enzymatic asymmetric hydrolysis of (1α,2β,3α)-2-(benzyloxymethyl)cyclopent-4-ene-1, 3-diol diacetate and enzymatic asymmetric acetylation of (1α,2β, 3α)-2-(benzyloxymethyl)cyclopent-4-ene-1,3-diol

Doi:10.1016/j.tetasy.2005.08.061
(2006)
Construction of azacycles by intramolecular amination of organoboronates and organobis(boronates)

Doi:10.1021/acs.orglett.1c00856
(2021)

Article Doi