Scholarly article on ethyl 5-amino-1-benzyl-1H-1,2,3-triazole-4-carboximidoate 20271-30-1 from Journal of the American Chemical Society p. 5832,5835

DOI: 10.1021/ja01603a033

Source and publish data:

Journal of the American Chemical Society p. 5832,5835 (1956)

Update date:2022-08-03

Topics:

Authors:

Hoover Hoover

Day Day

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

Article abstract of DOI:10.1021/ja01603a033

Full text of DOI:10.1021/ja01603a033

Products guided by the article

Product name:ethyl 5-amino-1-benzyl-1H-1,2,3-triazole-4-carboximidoate

Cas No:20271-30-1

R&D Labs maybe for 20271-30-1

JiangXi Keyuan Biopharma Co., LTD.

Contact:+86-563-6833666

Address:Guangde Fine Chemical Zone, Anhui Province, China
SICHUAN ZHONGBANG NEW MATERIAL CO., LTD

website:http://www.zhongbangst.com

Contact:86-830-2585019

Address:sichuan,china
Weihao Chemtech (ChangZhou) Co., Ltd.(expird)

Contact:051989185693

Address:NO 217 huangshan Rd ,Changzhou
MiHecb Bio-Tech Co., Ltd.

Contact:+86-0592 5353131

Address:No.56 Guani Road Software Park 2,Siming District
Luna Chemicals Co.,Ltd.

Contact:+86-570-4336358

Address:No.87 Building,Tianqian,Sidu Town

Relevant to this article

Macrocyclic bisindolylmaleimides: Synthesis by inter- and intramolecular alkylation

Doi:10.1021/jo971980h
(1998)
Asymmetric Total Synthesis of Hetidine-Type C₂₀-Diterpenoid Alkaloids: (+)-Talassimidine and (+)-Talassamine

Doi:10.1021/jacs.1c01865
(2021)
Nickle Catalysis Enables Access to Thiazolidines from Thioureas via Oxidative Double Isocyanide Insertion Reactions

Doi:10.1021/acs.orglett.8b03098
(2018)
Addition of allylstannanes to glycal epoxides. A diastereoselective approach to β-C-glycosidation

Doi:10.1016/S0040-4039(98)00138-5
(1998)
Eicosanoid biosynthesis: Differential inhibition of cytochrome P450 epoxygenase and ω-hydroxylase

Doi:10.1016/S0960-894X(97)10144-5
(1997)
Asymmetric addition of Davies's chiral lithium amide to prochiral vinyl phosphine oxides

Doi:10.1016/S0040-4039(97)10860-7
(1998)

Article Doi

DOI: 10.1021/ja01603a033