Results 121 to 130 of about 6,888 (163)
A new mesoporous Ce-Mn-LDH-based Co-MOF nano-composite for the green synthesis of tetrazoloquinazolines. [PDF]
Javadi S, Habibi D.
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Quinazolines. Part XV. Hexahydro- and octahydro-quinazolines
Journal of the Chemical Society C: Organic, 19713,4,5,6,7,8-Hexahydroquinazoline, obtained by catalytic reduction of 5,6,7,8-tetrahydroquinazoline, was slowly oxidised by air to the starting material in chloroform solution, but in aqueous alkali it was degraded to 2-formamidomethylcyclohexanone. trans-4a,5,6,7,8,8a-Hexahydroquinazolin-4(1 - or 3-H)-one was shown to be a tautomeric mixture of the (1H)
W. L. F. Armarego, Toshihiko Kobayashi
openaire +1 more source
Dermatitis from quinazoline oxide
Contact Dermatitis, 1986Dermatitis from 2‐chloromethyl‐4‐phenyl‐6‐chloroquinazoline‐3‐oxide, an intermediate product in the preparation of chlorodiazepoxide, is described in 29 workers at a pharmaceutical plant. All were patch test positive to quinazoline oxide (1%) and six to 0.05%. In most patients, the face was earlier and more severely involved than the hands.
P, Rebandel, E, Rudzki
openaire +2 more sources
ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
N. N. Tonkikh +2 more
openaire +1 more source
AbstractFor Abstract see ChemInform Abstract in Full Text.
N. N. Tonkikh +2 more
openaire +1 more source
Quinazolines. Part VIII. Electronic effects in 2-substituted quinazolines
Journal of the Chemical Society C: Organic, 1966In a study of the cations of twenty 2-substituted quinazolines, it was found that covalent hydration of the 3,4-double bond decreased according to the electronic effect of the 2-substituent; viz, +l > +M > –l. This is explained by the effect of the substituent on the polarity of the C-4, N-3 double bond. The effect of the acyl group on the rate of ring
W. L. F. Armarego, J. I. C. Smith
openaire +1 more source
Pharmacology, 1971
Piquizil, a 4-aminoquinazoline causing relaxation of respiratory smooth muscle in animals, appeared to be a bronchodilator in man. A metabolite of piquizil was isolated from human urine and identified. This metabolite, named hoquizil, had a longer plasma half-time than piquizil, was generally of comparable pharmacological activity, but was better ...
M. Schach von Wittenau, T.F. Brewer
openaire +1 more source
Piquizil, a 4-aminoquinazoline causing relaxation of respiratory smooth muscle in animals, appeared to be a bronchodilator in man. A metabolite of piquizil was isolated from human urine and identified. This metabolite, named hoquizil, had a longer plasma half-time than piquizil, was generally of comparable pharmacological activity, but was better ...
M. Schach von Wittenau, T.F. Brewer
openaire +1 more source
1984
Quinazoline (1) is a building block for approximately eighty naturally occurring alkaloids isolated from a number of families of the plant kingdom, from microorganisms and from animals. The first known quinazoline alkaloid was vasicine (peganine), isolated in 1888 from Adhatoda vasica, and later from other species.
openaire +2 more sources
Quinazoline (1) is a building block for approximately eighty naturally occurring alkaloids isolated from a number of families of the plant kingdom, from microorganisms and from animals. The first known quinazoline alkaloid was vasicine (peganine), isolated in 1888 from Adhatoda vasica, and later from other species.
openaire +2 more sources
Tetrahedron, 1986
Abstract Grignard reagents reacted with 2-aminobenzonitrile to give the intermediate 10 , which readily could be cyclized to quinazolines by reaction with carbonyl compounds (e.g. acid chlorides, anhydrides, formates and oxalates). The intermediate 10 and aldehydes, e.g.
Jan Bergman +3 more
openaire +1 more source
Abstract Grignard reagents reacted with 2-aminobenzonitrile to give the intermediate 10 , which readily could be cyclized to quinazolines by reaction with carbonyl compounds (e.g. acid chlorides, anhydrides, formates and oxalates). The intermediate 10 and aldehydes, e.g.
Jan Bergman +3 more
openaire +1 more source

