Reactions of N1-Hydroxyformamidines with Heterocumulenes

DOI: 10.1002/ardp.19813141206

Source and publish data:

Archiv der Pharmazie p. 1006 - 1014 (1981)

Update date:2022-08-04

Topics:

Authors:

Zinner, Gerwalt

Schecker, Heinz-Guenther

Heuer, Wilhelm

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

Article abstract of DOI:10.1002/ardp.19813141206

N¹-Hydroxyformamidines and isocyanates react to yield N¹-(carbamoyloxy)formamidines and/or 3-amino-1,2,4-oxazolidin-5-ones.Frequently the formation of ureas is observed.It can be explained by an oxidoreductive rearrangement to 1,3,5-trisubstituted biurets which undergo abstraction of isocyanate.Reactions with carbodiimides lead to 3-amino-5-imino-1,2,4-oxadiazolidines, ureas and carbodiimides not identical with the educts.

Full text of DOI:10.1002/ardp.19813141206

Products guided by the article

Product name:1-tert-Butyl-3,5-di(4-tolyl)biuret

Cas No:80820-85-5

R&D Labs maybe for 80820-85-5

SuZhou Bichal Biological Technology CO.,LTD

Contact:+86-512-68051130

Address:NO.32 huoju road HI-TECH Industrial development zone SuZhou China
Shanghai Yingrui Biopharma Co., Ltd

Contact:021-3358 8661*8003

Address:shanghai
Shenzhen Feiming Science and Technology Co,. Ltd

Contact:+86-755-85232577

Address:#B2309, Fenglin International Center ,Jixiang Road, Longcheng street, LongGang District, Shenzhen city, Guangdong province, China.
Guangzhou Chemical Reagent Factory

Contact:+86-20-8435 9820 or 8435 7345

Address:Southern Guangzhou, Guangdong, China
Yangling Ciyuan biotech Co., Ltd.

Contact:86-15802970736

Address:2-1804, International Park Mansion, No.2, South Fengdeng Road, Lianhu District

Relevant to this article

Cyclization of Conjugated Azines. Synthesis and Thermal Rearrangements of 1,8-Diaryl-4,5-diaza-3-methyl- and 3-phenyl-1,3,5,7-octatetraenes (α,β-Unsaturated Azines) to 1-(1-Methyl-3-phenyl- and -1,3-diphenyl-1-propenyl)-5-arylpyrazoles

Doi:10.1021/jo00348a008
(1982)
SENSITIZED PHOTOLYSIS OF BENZOYL AZIDE. A NITRENE SINGLET-TRIPLET EQUILIBRIUM

Doi:10.1246/cl.1982.9
(1982)
Protective group-free syntheses of (±)-frontalin, (±)-endo-brevicomin, (±)-exo-brevicomin, and (±)-3,4- dehydro-exo-brevicomin: Racemic pheromones with a 6,8-dioxabicyclo[3.2.1]octane ring

Doi:10.1271/bbb.110071
(2011)
Adriamycin Analogues. Preparation of 9,10-Anhydrodaunorubicin, 9,10-Anhydroadriamycin, and Some Related Compounds

Doi:10.1021/jm00346a027
(1982)
Synthesis and Ring -Opening Reactions of Functionalized Spiro-Δ³-1,2,3-thiadiazoline 1-Oxides and 1,1-Dioxides. A New Approach to Unsymmetrically Disubstituted α-Chloro Azines

Doi:10.1021/jo00141a012
(1982)
Synthesis and vasodilator effects of rutaecarpine analogues which might be involved transient receptor potential vanilloid subfamily, member 1 (TRPV1)

Doi:10.1016/j.bmc.2009.02.015
(2009)

Article Doi