Synthesis of some 1,2-Dihalogenonorbornanes

DOI: 10.1002/hlca.19820650710

Source and publish data:

Helvetica Chimica Acta p. 2029 - 2041 (1982)

Update date:2022-09-26

Topics:

Authors:

Krebs, Ernst-Peter

Keese, Reinhart

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

Article abstract of DOI:10.1002/hlca.19820650710

The synthesis of 1,2exo-dibromo-norbornane as well as the preparation of the configurational isomers of 2-bromo-1-iodo- and 2-chloro-1-iodo-norbornane are described.

Full text of DOI:10.1002/hlca.19820650710

Products guided by the article

Product name:Bicyclo[2.2.1]heptane-1-carbonyl chloride, 2-chloro-, endo- (9CI)

Cas No:85173-68-8

R&D Labs maybe for 85173-68-8

QINGDAO DEVELOP chemistry Co.,Limited

Contact:+86-532-85807910

Address:98#Nanjing Road, Qingdao, China 266071
Heliosense Biotechnologies, Inc.

website:https://www.heliosense.com/

Contact:+86-592-5667290

Address:Xiamen Torch Hi-tech Zone Venture Weiye Building S506
Jiangsu Jiuri Chemical Co.,Ltd.

Contact:+86-519-82118868

Address:Tianwang Town, Jurong City, Jiangsu Province, China
Shandong Yuanli Science and Technology Co., Ltd.

Contact:86-0536-6777557

Address:Zhuliu Industiral Park,Changle County
FREEBARQUE DEVELOPMENT GROUP LIMITED

Contact:+86(0)10-5109 5335 or 5109 5345

Address:Room602,Block1-B,LINGDI OFFICE,NO.13 BEIYUAN ROAD

Relevant to this article

6-(2-Furanyl)-9H-purin-2-amine derivatives as A_2A adenosine antagonists

Doi:10.1016/j.bmcl.2005.02.031
(2005)
DIHYDROSILAANTHRACENYLIDENE AND DIHYDROANTHRACENYLIDENE

Doi:10.1016/S0040-4039(00)88356-2
(1982)
Symmetrical Monothiopyrophosphate

Doi:10.1021/ja00348a054
(1983)
A Regio- and Stereodivergent Synthesis of Homoallylic Amines by a One-Pot Cooperative-Catalysis-Based Allylic Alkylation/Hofmann Rearrangement Strategy

Doi:10.1002/anie.201905426
(2019)
One-pot synthesis of functionalized nitrones from nitro compounds

Doi:10.1055/s-2001-16042
(2001)
Palladium-catalyzed one-step synthesis of symmetrical diaryl sulfones from aryl halides and a sulfur dioxide surrogate

Doi:10.1246/cl.190300
(2019)

Article Doi