v-Triazolines. Part XIX. Thiocino[4,5-d]-1,2,3-triazole and thiocino[4,5-d]isoxazole derivatives

DOI: 10.1002/jhet.5570210438

Source and publish data:

Journal of Heterocyclic Chemistry p. 1121 - 1123 (1984)

Update date:2022-08-04

Topics:

Authors:

Almirante

Forti Forti

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

Article abstract of DOI:10.1002/jhet.5570210438

Full text of DOI:10.1002/jhet.5570210438

Products guided by the article

Product name:1-(4-Nitrophenyl)-9a-pyrrolidino-1,3a,4,5,7,8,9,9a-octahydrothiocino<4,5-d>-1,2,3-triazole

Cas No:93582-87-7

R&D Labs maybe for 93582-87-7

Acros Pharmatech Limited

website:http://www.acrospharmatech.com

Contact:+1-3234804688

Address:Flat/RM 1502,Easey Commercial building 253-261 Hennessy Road,Wanchai，HongKong
Hangzhou Sartort Biopharma Co., Ltd

website:http://www.sartort.com

Contact:86-571-87039693

Address:No. 57, Tech Park Road, Hangzhou, Zhejiang, China
Wuhan HengHeDa Pharm Co., Ltd

Contact:86-27-84888681

Address:Wuhan economic & technology development zone
Zhejiang Newfine Industry Co.,Ltd.

Contact:+86-573-82262042

Address:No.225,Dongqing Road, garoms@163.com
Chongqing Shuangfeng Chemical Co.,Ltd

Contact:+86-23-49850156

Address:No.663,xuanhua Rd,yongchuan,chongqing,China

Relevant to this article

Addition of organometallic reagents to nitriles promoted by titanium(IV) isopropoxide as a procedure of synthesis of primary tert-alkylamines

Doi:10.1134/S1070428007100016
(2007)
A simple synthesis of furo[3′,4′:5,6]pyrido[2,3-d]pyrimidine derivatives through multicomponent reactions in water

Doi:10.1002/ejoc.200600913
(2007)
A New Synthesis of α-Methylene Lactones

Doi:10.1039/c39840000132
(1984)
BROMINATION OF 8R-4-PHENYL-2,3-DIHYDRO-1H-1,5-BENZODIAZEPINONES-2

Doi:10.1007/BF00513586
(1984)
Preparation of the 5/5-spiroketal of the ritterazines

Doi:10.1021/jo0626461
(2007)
Scandium and gadolinium complexes with aryldiimine NCN pincer ligands: Synthesis, characterization, and catalysis on isoprene and 1,5-hexadiene polymerization

Doi:10.1016/j.poly.2018.02.010
(2018)

Article Doi