2-amino-1,3,4-oxadiazoles. 32. Ring opening of 2-imino-3-alkyl-5-aryl-1,3,4-oxadiazolines with carbazinic acid ethyl ester and consecutive reactions

DOI: 10.1002/ardp.19703030313

Source and publish data:

Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft p. 263 - 267 (1970)

Update date:2022-08-02

Topics:

Authors:

Gehlen Gehlen

Demin Demin

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

Article abstract of DOI:10.1002/ardp.19703030313

Full text of DOI:10.1002/ardp.19703030313

Products guided by the article

Product name:5-(N'-benzoyl-N-methyl-hydrazino)-1,2-dihydro-[1,2,4]triazol-3-one

Cas No:27048-44-8

R&D Labs maybe for 27048-44-8

Huludao Tianqi Shengye Chemical Co.,Ltd.

Contact:0086 429 2075777

Address:Area B,Shipbuilding Industry Park,Beigang District,Huludao City,Liaoning prov.,China
Xiamen Kaijia Imp & Exp Co., Ltd.

Contact:86-592-5101177

Address:Room406 Luhui Building No. 65 Haitian Road Huli Xiamen,China.
Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China
Suzhou HeChuang Chemical Co.,Ltd.

Contact:+86-512-88800520

Address:No.9 Guanchao Rd,Changshu Advanced Materials Industy Park
ZHEJIANG SYNOSE TECH CO.,LTD.

website:https://www.synose.com/

Contact:86-579-82275537

Address:No.1958 Liyu Road , jinhua,zhejiang,China

Relevant to this article

Acylimine mediated N-N bond cleavage of pyrazolidinediones and subsequent conversion to dihydropyrimidinediones and malonamides

Doi:10.1016/S0040-4039(00)01865-7
(2001)
Doi:10.1021/jo00803a028
(1971)
A scaleable synthesis of fiduxosin

Doi:10.1021/op049889k
(2004)
A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro

Doi:10.1016/S0960-894X(00)00110-4
(2000)
3-(tributylstannyl)allyl alcohols: Useful building blocks for solid-phase synthesis of skipped dienes and trienes

Doi:10.1135/cccc20000434
(2000)
Doi:10.1021/ja00715a033
(1970)

Article Doi