Scholarly article on O--serinpropylamid p-toluolsulfonsaeure-salz 100233-12-3 from Journal of the American Chemical Society p. 4716 - 4720

DOI: 10.1021/ja01075a037

Source and publish data:

Journal of the American Chemical Society p. 4716 - 4720 (1964)

Update date:2022-08-03

Topics:

Authors:

Ginsburg,S.

Wilson,I.B.

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

Article abstract of DOI:10.1021/ja01075a037

Full text of DOI:10.1021/ja01075a037

Products guided by the article

Product name:O-<4-Nitro-benzoyl>-serinpropylamid p-toluolsulfonsaeure-salz

Cas No:100233-12-3

R&D Labs maybe for 100233-12-3

Tianfusheng Bio-tech Co., Ltd.

Contact:+86-0312-5907251

Address:hebei
QINGDAO DEVELOP chemistry Co.,Limited

Contact:+86-532-85807910

Address:98#Nanjing Road, Qingdao, China 266071
Chengdu Pukang Biotechnology Co., Ltd

Contact:+86-28-82550498

Address:No. 558 Rulin Road,Xinjin county,Chengdu city, China
Nanjing Habo Medical Technology Co., Ltd.

Contact:025－85769882

Address:No.108. Ganjiabian east. Qixia District .Nanjing
guide(suzhou) fine materials co. ltd

Contact:0512-80972173

Address:21st Building, No.369 Lushan Rd, New District Suzhou China 215129

Relevant to this article

Reusable Ce-V Loaded Alumina Catalyst for Multicomponent Synthesis of Substituted Pyridines in Green Media

Doi:10.1002/jhet.2430
(2016)
Synthesis of the first representatives of benzannelated dihydroselenochromenes [4]

Doi:10.1007/s10593-006-0253-5
(2006)
Total synthesis of polydiscamides B, C, and D via a convergent native chemical ligation-oxidation strategy

Doi:10.1021/ol502045u
(2014)
N -Isopropylsulfinylimines vs. N-tert -butylsulfinylimines in the stereoselective synthesis of sterically hindered amines: An improved synthesis of enantiopure (R)- And (S)-rimantadine and the trifluoromethylated analogues

Doi:10.1039/c9ob02241d
(2019)
New synthesis and thermal studies of palladacycloalkanes and their precursors

Doi:10.1016/j.jorganchem.2007.10.025
(2008)
Catalyst-free synthesis of quinoxalines

Doi:10.14233/ajchem.2015.18680
(2015)

Article Doi

DOI: 10.1021/ja01075a037