A Novel Thermal Rearrangement of Allylic Nitro Derivatives into Allylic Alcohols

DOI: 10.1039/c39890001006

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1006 - 1008 (1989)

Update date:2022-08-03

Topics:

Authors:

Boivin, Jean

Kaim, Laurent El

Kervagoret, Jocelyne

Zard, Samir Z.

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

Article abstract of DOI:10.1039/c39890001006

Heating secondary and tertiary allylic nitro compounds gives the corresponding rearranged allylic alcohols in moderate to good yield.

Full text of DOI:10.1039/c39890001006

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:anti-2-ethylidene cyclohexanol

Cas No:1219025-32-7

R&D Labs maybe for 1219025-32-7

Ningbo Huajia Chemicals

Contact:+86-574-87065746

Address:10th Floor, No.787 Baizhang East Road,
Anyang Double Circle Auxiliary CO.,LTD

Contact:0086-134 6082 4403

Address:dongfeng road, anyang city, henan province,china
zonk drug r&d limited

Contact:+86-20-32051076

Address:1105,Building A, International Business Incubator,Science City
Santow Laboratory Limited

Contact:+86-371-55981030

Address:Room 1571, Macalline Soho, No.1, Shangdu Road, Zhengzhou, Henan
Jiangsu Mingchem Corporation

website:http://www.mingchem.com/en/index

Contact:0519-85170101-802

Address:Fifth Floor,B of Beihua Buliding,520 Road of Science and Education City,Changwu middle road NO.801,Wujin District,Changzhou,Jiangsu province

Relevant to this article

Thioether-promoted direct olefination of polyfluoroarenes catalyzed by palladium

Doi:10.1021/ol402492s
(2013)
2,3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity

Doi:10.1016/j.bmc.2010.01.009
(2010)
Determination of critical micelle concentration by hyper-Rayleigh scattering

Doi:10.1021/ja029070r
(2003)
An efficient entry to 1,2-benzisoxazoles via 1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne

Doi:10.1039/b927235f
(2010)
Synthesis of a proposed biosynthetic intermediate of a marine cyclic ether brevisamide for study on biosynthesis of marine ladder-frame polyethers

Doi:10.1016/j.tetlet.2010.01.013
(2010)
Practical Gram-Scale Synthesis of Iboxamycin, a Potent Antibiotic Candidate

Doi:10.1021/jacs.1c03529
(2021)

Article Doi