Study of the Conformation of Novel N-Nitrosothioureas by High-Field Nitrogen-15 and Carbon-13 Nuclear Magnetic Resonance Spectroscopy Employing Specifically Labeled Compounds

DOI: 10.1021/jo00152a020

Source and publish data:

Journal of Organic Chemistry p. 513 - 520 (1983)

Update date:2022-08-03

Topics:

Authors:

Lown, J. William

Chauhan, Shive M. S.

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

Article abstract of DOI:10.1021/jo00152a020

The synthesis of certain specifically ¹³C=S and N₁, N₃, and N=O ¹⁵N-labeled novel N-nitrosothioureas is described.A detailed study of their high-field ¹³C and ¹⁵N NMR parameters was perform

Full text of DOI:10.1021/jo00152a020

Products guided by the article

Product name:3-cyclohexyl-1-ethyl-1-(nitroso-¹⁵N)thiourea-3-¹⁵N

Cas No:84051-06-9

R&D Labs maybe for 84051-06-9

BIOS CHEMICALS

Contact:+33-5-34012600

Address:28 ZA des Pignès
Maithili Life Sciences

Contact:+91 9963263336

Address:Plot#146A, IDA Mallapur, Hyderabad - 500072
Nanjing Habo Medical Technology Co., Ltd.

Contact:025－85769882

Address:No.108. Ganjiabian east. Qixia District .Nanjing
Taiwan Surfactant Corp.

Contact:886 2 2541 0022

Address:8 Fl., No. 11, Sec. 1, Chung Shan North Rd., Taipei, Taiwan R.O.C.
A-Chem Technologies Co.,Ltd.

Contact:+86-512-69561895

Address:No.111, Building A4, 218 Xinghu Street, Suzhou Industrial Park, P. R. China

Relevant to this article

Doi:10.1016/S0020-1693(00)85027-6
(1982)
Hydrates and ammonium salts of 4-nitrobenzenesulfonic acid: Supramolecular organization and its relation to proton conductivity

Doi:10.1007/s11172-011-0187-7
(2011)
THIAZOLIDINES WITH ADAMANTYL SUBSTITUENTS

Doi:10.1007/BF00772175
(1982)
Cavernosine, a novel ichthyotoxic terpenoid lactone from the sponge Fasciospongia cavernosa

Doi:10.1002/bscb.19820910907
(1982)
ESR Investigation of Radical Cations Formed from Aromatics and Heteroaromatics Adsorbed on Mo-Al2O3 Surfaces

Doi:10.1021/j100446a019
(1980)
Synthesis and anticancer activity evaluation of 3-(4-oxo-2-thioxothiazolidin-5-yl)-1H-indole-carboxylic acids derivatives

Doi:10.1080/00397911.2020.1786124
(2020)

Article Doi