A Simple Preparation of 1,2-Dihydropentalene from Cyclooctatetraene

DOI: 10.1055/s-1987-28009

Source and publish data:

Synthesis p. 573 - 574 (1987)

Update date:2022-08-23

Topics:

Authors:

Meier, Herbert

Pauli, Alfred

Kochhan, Peter

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

Article abstract of DOI:10.1055/s-1987-28009

Flash thermolysis of cyclooctatetraene leads to a mixture of four isomeric dihydropentalenes 1,3,4 and 5.Catalytic hydrogen transfer on basic alumina or silica gel furnishes pure 1,2-dihydropentalene (1).

Full text of DOI:10.1055/s-1987-28009

Products guided by the article

Product name:1,2-dihydropentalene

Cas No:30294-54-3

R&D Labs maybe for 30294-54-3

shanghai jiuling chemical co.,ltd.

Contact:+86-21-50387295

Address:Zaozhuang Road, Pudong, Shanghai City. China
Chengdu Shengnuo Biological Technology Co., Ltd.

Contact:86-028-85275045

Address:Sichuan Province Chengdu hi tech Zone Tianfu Avenue North of 1480
Nanjing Fayekong Chemcial Co.,Ltd(expird)

Contact:86-25-58813444

Address:Rm 1503, Unit 1, Building 5, Zijinnanyuan, Nanjing, Jiangsu, China
shanghai tuomiao chemicial co.,ltd.

website:https://www.tuomiaochem.com/

Contact:021 - 59853336

Address:shanghai
Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi

Relevant to this article

Catalytic Leuckart-Wallach-type reductive amination of ketones

Doi:10.1021/jo0203701
(2002)
Artificial molecular clamp: A novel device for synthetic polymerases

Doi:10.1002/anie.201102834
(2011)
Copper-mediated Chan-Evans-Lam N-arylation of 5-methylene-4-aryl-1,5-dihydro-2H-pyrrol-2-one derivatives

Doi:10.1016/j.tetlet.2018.01.039
(2018)
Doi:10.1021/ja01367a043
(1930)
Doi:10.1359/jbmr.2001.16.2.221
(1871)
Asymmetric Cross-coupling of Organozinc Reagents with Alkenyl Bromides Catalyzed by a Chiral Ferrocenylphosphine-Palladium Complex

Doi:10.1246/bcsj.56.363
(1983)

Article Doi