REGIOSPECIFIC ADDITIONS OF SOME SIMPLE DIENES TO HALOQUINONES

DOI: 10.1016/S0040-4039(00)81953-X

Source and publish data:

Tetrahedron Letters p. 2453 - 2456 (1983)

Update date:2022-08-17

Topics:

Authors:

Boisvert, Louise

Brassard, Paul

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

Article abstract of DOI:10.1016/S0040-4039(00)81953-X

Some simple dienes have been shown to react regiospecifically with haloquinones; the adducts can be oxidized without loss of the oxygenated function or aromatized to a variety of natural products and useful intermediates.

Full text of DOI:10.1016/S0040-4039(00)81953-X

Products guided by the article

Product name:2-Chloro-1,4-naphthoquinone

Cas No:1010-60-2

R&D Labs maybe for 1010-60-2

Foreschem Co., Ltd

Contact:+86-533-3112891

Address:zibo
Zhejiang Genebest Pharmaceutical Co.,Ltd.

Contact:0086-571-63532866

Address:No.1 Jinboshi Rd Lishan Town Fuyang City Zhejiang Province China
Zhejiang Allied Chemical Co.,Ltd

Contact:18967038207

Address:Area A-30, High-tech Industrial Park, Quzhou, Zhejiang, China.
Hangzhou jls Flame Retardants Chemical Co.,Ltd

Contact:+86-571-87250387/87250386

Address:MOGANSHAN RODA 1418# SHANGCHENG INDUSTRIAL PARK
Jinhua Haoyuan Chemical CO., LTD(expird)

Contact:86-579-82465583

Address:Jinhua,Zhejiang

Relevant to this article

Substituted halogenated arylsulfonamides: A new class of σ receptor binding tumor imaging agents

Doi:10.1021/jm9800447
(1998)
Synthesis and stability studies of Ga-67 labeled phosphonium salts

Doi:10.1002/jlcr.3448
(2017)
Application of pentacoordinated spirophosphorane as a new organocatalyst for the Michael addition reaction

Doi:10.1080/10426507.2021.1946062
(2021)
Aryl Fluorides from the Reaction of Boron Trifluoride with Aryl-lead(IV) Triacetates, which may be generated in situ from Aryltrimethylsilanes, Triarylboroxines, and Arenes

Doi:10.1039/C39900001065
(1990)
Catalytic reduction of NO by CO over rhodium catalysts. 3. The role of surface isocyanate species

Doi:10.1006/jcat.2000.2892
(2000)
Doi:10.1016/S0040-4020(01)82717-4
(1969)

Article Doi