Approaches to analogs of anhydrogliotoxin.

DOI: 10.1021/ja00787a045

Source and publish data:

Journal of the American Chemical Society p. 1989 - 1996 (1973)

Update date:2022-08-03

Topics:

Authors:

Ottenheym

Spande Spande

Witkop Witkop

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

Article abstract of DOI:10.1021/ja00787a045

Full text of DOI:10.1021/ja00787a045

Products guided by the article

Product name:(2R,9aR)-9,9-Dimethyl-2-methylamino-3-oxo-2,3-dihydro-9H-thiazolo[3,2-a]indole-9a-carboxylic acid ethyl ester

Cas No:41168-20-1

R&D Labs maybe for 41168-20-1

He Bei Shun Er Chemical Co., LTD.

Contact:86-0311-86996932/86860168

Address:No 18,North street
SINFACHEM LIMITED

Contact:86-25-84683399

Address:605, Phoenix Herui Plaza, No.389, South Taiping Road, Nanjing, China 210002
Shanghai Mio Chemical Co., Ltd

Contact:0086 21- 64401188-622

Address:16 Floor NO.2 Jiefang Building, No. 4855 Dushi Road, 201100 Shanghai, P.R.China
Suzhou HeChuang Chemical Co.,Ltd.

Contact:+86-512-88800520

Address:No.9 Guanchao Rd,Changshu Advanced Materials Industy Park
SAGECHEM LIMITED

website:http://www.sagechem.com

Contact:+86-571-86818502

Address:Room C1301, New Youth Plaza, 8 Jia Shan Road, Hangzhou, China

Relevant to this article

Oxidovanadium(IV/V) complexes as new redox mediators in dye-sensitized solar cells: A combined experimental and theoretical study

Doi:10.1021/acs.inorgchem.5b00159
(2015)
Concise synthesis of a steroid C/D-ring system using a bicyclo[3.2.1]octane chiral building block: A new route to 25-hydroxy-Grundmann's ketone

Doi:10.1055/s-2002-19353
(2002)
Synthesis of pyrazolidine, 1-pyrazoline, 2-pyrazoline derivatives by selenium-induced cyclization of homoallylhydrazines

Doi:10.1016/S0040-4020(01)01064-X
(2001)
Doi:10.1055/s-1973-22155
(1973)
Specific Phase-Transfer Catalyzed N-Monoalkylation of 2-Aminobenzophenones

Doi:10.1055/s-1981-29477
(1981)
Studies on polypeptides, III. The synthesis of five C-peptide sequences of porcine proinsulin for immunological studies.

Doi:10.1515/bchm2.1973.354.1.141
(1973)

Article Doi