Scholarly article on 3,4-di-tert-butyl-[1,3,4]oxadiazolidine 300702-60-7 from Journal of the American Chemical Society p. 7108 - 7113

DOI: 10.1021/ja00775a040

Source and publish data:

Journal of the American Chemical Society p. 7108 - 7113 (1972)

Update date:2022-08-05

Topics:

Authors:

Nelsen,S.F.

Hintz,P.J.

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

Article abstract of DOI:10.1021/ja00775a040

Full text of DOI:10.1021/ja00775a040

Products guided by the article

Product name:3,4-di-tert-butyl-[1,3,4]oxadiazolidine

Cas No:300702-60-7

R&D Labs maybe for 300702-60-7

Yingkou Sanzheng New Technology Chemical Industry Co., Ltd.

Contact:+86-417-2927806

Address:yingkou
Beijing Mashi Fine Chemical Co.,Ltd.

Contact:+86-10-61271592

Address:Room 506, Section B, Kaichi Mansion, Industrial Development
Ningbo Bichem Pharmaceutical Co.,Ltd

Contact:18957868060 057487816388

Address:ningbo
TIC Gums, Inc.

Contact:410-273-7300; 800-221-3953

Address:4609 Richlynn Dr., PO Box 369, Belcamp, MD, 21017-0369, USA
Shanghai Balmxy Pharmaceutical Co., Ltd

Contact:0086-21-24206007

Address:Room 402, 15#, No. 909 wangyue Road, shanghai, P. R. China

Relevant to this article

THE SYNTHESIS OF 3-FLUOROASPARATIC ACID

Doi:10.1016/S0022-1139(00)83058-4
(1988)
Glucose-based spiro-isoxazolines: A new family of potent glycogen phosphorylase inhibitors

Doi:10.1016/j.bmc.2009.08.060
(2009)
Design and synthesis of potent and orally active GPR4 antagonists with modulatory effects on nociception, inflammation, and angiogenesis

Doi:10.1016/j.bmc.2017.06.050
(2017)
[Fesipmim]Cl as highly efficient and reusable catalyst for solventless synthesis of dihydropyridine derivatives through Hantzsch reaction

Doi:10.1007/s12039-020-01770-9
(2020)
5-(1,2,3-Triazol-l-yl)tetrazole derivatives of an azidotetrazole via click chemistry

Doi:10.1002/chem.200901029
(2009)
Ruthenium-catalyzed direct C3 alkylation of indoles with α,β-unsaturated ketones

Doi:10.1039/c4ob02124j
(2015)

Article Doi

DOI: 10.1021/ja00775a040