Results 131 to 140 of about 433,597 (216)

Nucleophilic Addition of Amines to Ruthenium Carbenes: ortho‐(Alkynyloxy)benzylamine Cyclizations towards 1,3‐Benzoxazines [PDF]

open access: yesAngewandte Chemie - International Edition, 2015
NOTICE: This is the peer reviewed version of the following article: González-Rodríguez, C., Suárez, J. R., Varela, J. A., Saá, C. (2015). Nucleophilic Addition of Amines to Ruthenium Carbenes: ortho‐(Alkynyloxy)benzylamine Cyclizations towards 1,3 ...
CARLOS Gonzalez-Rodriguez   +2 more
exaly   +3 more sources

Reagent-Controlled Divergent Synthesis of 2-Amino-1,3-Benzoxazines and 2-Amino-1,3-Benzothiazines.

open access: yesJournal of Organic Chemistry, 2019
A reagent-controlled chemoselective process has been devised for the synthesis of 4H-1,3-benzoxazines and related biologically important heterocycles in high yields under mild conditions.
V. P. R. K. Putta   +7 more
semanticscholar   +4 more sources

Access to Chiral Tetrahydroquinazolines/1,3-Benzoxazines via Iridium-Catalyzed Asymmetric [4 + 2] Cycloaddition.

open access: yesOrganic Letters, 2023
An iridium-catalyzed asymmetric [4 + 2] cycloaddition of 1,3,5-triazinanes with 2-(1-hydroxyallyl)anilines/2-(1-hydroxyallyl)phenols has been developed, providing a straightforward and efficient approach to a wide range of tetrahydroquinazolines in good ...
Shengbiao Tang   +4 more
semanticscholar   +2 more sources

Synthesis of 1,3-benzoxazines Based on 2,4,4-trimethyl-7,2’,4’-trihydroxy Flavan: Antibacterial, Anti-inflammatory, Cyclooxygenase-2 Inhibition and Molecular Modelling Studies

open access: yesLetters in Drug Design & Discovery, 2018
In the present study, the formation of 2, 4, 4-trimethyl-7,2’4’-trihydroxy flavan has been used as the key feature for the formation of new 1,3-benzoxazines.
I. Mohammed   +5 more
semanticscholar   +3 more sources

Synthesis of Substituted 1,3-Benzoxazines and Their Anticorrosion Activity

Russian Journal of General Chemistry
R. R. Safargalin   +3 more
semanticscholar   +2 more sources

Visible-light-catalyzed synthesis of 1,3-benzoxazines via formal [4 + 2] cycloaddition of oximes with o-hydroxybenzyl alcohols.

Organic and biomolecular chemistry, 2023
A formal [4 + 2] cycloaddition of oximes with o-hydroxybenzyl alcohols was developed to easily synthesize diverse 1,3-benzoxazine derivatives. This synthesis was achieved under visible light-based organocatalytic and TsOH conditions.
Zhenjie Qi   +5 more
semanticscholar   +1 more source

Design, Spectroscopic Studies, DFT Calculations and Evaluation of Biological Activity of Novel 1,3-Benzoxazines Encompassing Isoniazid

Polycyclic aromatic compounds (Print), 2021
It was planned to utilize isoniazid 1 and substituted salicylaldehydes 2a–f to synthesize some N'-[(E)-(substituted-2-hydroxyphenyl)methylidene]pyridine-4-carbohydrazides 3a–g.
Basavarajaiah Suliphuldevara Matada   +2 more
semanticscholar   +1 more source

Synthesis and antimicrobial activity of new benzofuranyl-1,3-benzoxazines and 1,3-benzoxazin-2-ones

Journal of Heterocyclic Chemistry, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Ravi K. Ujjinamatada   +2 more
openaire   +1 more source

Synthesis of 4H-1,3-benzoxazin-4-onium salts and 4-H-1,3-benzoxazin-4-ones

Chemistry of Heterocyclic Compounds, 1975
Salicylamide and its substituted derivatives react with aliphatic carboxylic acid anhydrides and perchloric acid to give 4H-1,3-benzoxazin-4-onium salts. These same compounds were obtained by acidic cyclization of O- and N-acylsalicylamides. The synthesized salts are converted to 2-substituted 4H-1,3-benzoxazin-4-ones by the action of triethylamine and
Yu. I. Ryabukhin   +2 more
openaire   +1 more source

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