Depsidone Synthesis. Part 17. The Photochemistry of Grisa-3',5'-diene-2',3-diones

DOI: 10.1039/P19810000870

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 870 - 873 (1981)

Update date:2022-08-05

Topics:

Authors:

Sala, Tony

Sargent, Melvyn V.

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

Article abstract of DOI:10.1039/P19810000870

The photoconversion of spiro-2',3(2H)-diones (grisa-3',5'-diene-2',3-diones) to dibenzofurans is described, and a mechanism for this reaction is proposed.

Full text of DOI:10.1039/P19810000870

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

View Article Online

Products guided by the article

Product name:7-benzyloxy-1,3,8-trichloro-2-methoxy-4,9-dimethyldibenzofuran

Cas No:69709-86-0

R&D Labs maybe for 69709-86-0

Chengda Pharmaceuticals Co., Ltd.

Contact:+86-573-84601188

Address:hengshan Road 5# in Jiashan, zhejiang
Hubei Xiangxi Chemical Industry Co.,Ltd

Contact:+86-710-3454830

Address:No.7, Daqing East Road, Xiangfan City, Hubei Province, China
Ningbo Huajia Chemicals

Contact:+86-574-87065746

Address:10th Floor, No.787 Baizhang East Road,
Hangzhou Mole's Science & Technology Co.,Ltd.(expird)

Contact:+86-571-56880228

Address:15F Guodu development Building, NO.182 Zhaohui Road
Jiaxing Trustworthy Import And Export Co.,Ltd

Contact:+86-573-82030555

Address:Room 1202, Unit B, Charming plaza,No.1558 East Zhongshan Road , Jiaxing City, Zhejiang Province, China.

Relevant to this article

Microwave-assisted efficient synthesis of benzo[4,5]imidazo[1,2-a] pyrimidine derivatives in water under catalyst-free conditions

Doi:10.1002/jhet.5570440625
(2007)
Doi:10.1021/ja01138a045
(1952)
Total Synthesis and Preliminary Biological Evaluation of cis-Solamin Isomers

Doi:10.1021/jo049909g
(2004)
Doi:10.1016/S0040-4039(00)70556-9
(1978)
2-Styryl-pyridines and 2-(3,4-Dihydro-naphthalen-2-yl)-pyridines as potent NR1/2B subtype selective NMDA receptor antagonists

Doi:10.2533/000942904777677579
(2004)
Doi:10.1021/ja01261a606
(1942)

Article Doi