Results 81 to 90 of about 2,756 (214)

Synthesis of benzofurans and benzopyrans

open access: yes, 2002
Syntheses of 2,3-dihydrobenzofurans and 3,4-dihydrobenzopyrans normally involve several stages, therefore efficient syntheses of these compounds are desirable. A number of 3,4-dihydrobenzopyrans derivatives were prepared in one pot syntheses. The reaction is thought to proceed through cation intermediates, involving allylic cations generated by the ...
openaire   +2 more sources

Safety and Efficacy of Direct Oral Anticoagulants Versus Vitamin K Antagonists for Cerebrovascular Ischemic Outcomes in Non‐Valvular Atrial Fibrillation: A Systematic Review and Meta‐Analysis

open access: yesClinical Cardiology, Volume 49, Issue 4, April 2026.
Direct Oral Anticoagulants (DOACs) were associated With lower rates of cerebrovascular ischemic events and major bleeding compared With Vitamin K antagonists in non‐valvular atrial fibrillation, With similar mortality. These findings support DOACs as the preferred anticoagulant strategy for stroke prevention in contemporary clinical practice.
Anam Nasir   +8 more
wiley   +1 more source

Synthesis of Benzopyrans by Pd(II)- or Ru(II)-Catalyzed C–H Alkenylation of 2‑Aryl-3-hydroxy-2-cyclohexenones

open access: yes, 2016
2-Aryl-3-hydroxy-2-cyclohexenones are shown to be competent substrates for palladium- and ruthenium-catalyzed C–H alkenylation reactions with terminal alkenes, providing, in most cases ...
Hon Wai Lam (1932658)   +3 more
core   +1 more source

Heteroaromatization with 4-Hydroxycoumarin Part II: Synthesis of Some New Pyrano[2,3-d]pyrimidines, [1,2,4]triazolo[1,5-c]pyrimidines and Pyrimido[1,6-b]-[1,2,4]triazine Derivatives

open access: yesMolecules, 2001
A variety of novel [1,2,4]triazolo[1,5-c]pyrimidine-13-ones (4a-f) and (5b-d) could be obtained via reaction of 9-amino-7-(4’-chlorophenyl)-8,9-dihydro-8-imino-6H,7H-[1]benzopyrano[3`,4`:5,6]pyrano[2,3-d]pyrimidine-6-one (3) with a variety of ...
A. H. Bedair   +4 more
doaj   +1 more source

Asymmetric Roadmap to Diverse Polycyclic Benzopyrans via Phosphine-Catalyzed Enantioselective [4 + 2]-Annulation Reaction

open access: yes, 2016
The catalytic addition of the amino acid derived bifunctional N-acylamino­phosphine to an α-substituted allene ester generated a zwitterionic dipole that engaged the vinylogous ester function of 3-cyano-chromones in a [4 + 2] annulation reaction to ...
Carsten Strohmann (1307016)   +14 more
core   +2 more sources

Synthesis and Chemical Properties of 3-Phosphono-coumarins and 1,2-Benzoxaphosphorins as Precursors for Bioactive Compounds

open access: yesMolecules, 2019
Coumarins are an important class of natural heterocyclic compounds that have attracted considerable synthetic and pharmacological interest due to their various biological activities.
Ana I. Koleva   +2 more
doaj   +1 more source

Sc(OTf)3-catalyzed diastereoselective synthesis of 3,4-dihydro-4-amino-2H-1-benzopyrans

open access: yes, 2001
2,2-Dimethoxypropane reacts with a variety of o-hydroxybenzaldimines in the presence of a catalytic amount of scandium triflate at ambient temperature to afford a series of new compounds, 3,4-dihydro-4-amino-2-methoxy-2-methyl-2H-1-benzopyrans, in high ...
Chandra Sekhar, K.   +3 more
core   +1 more source

Trifluoroacetic acid-mediated facile transformation of 2-C-hydroxymethyl-D-glycals to chiral pyrano[2,3-b]benzopyrans

open access: yes, 2009
Treatment of 2-C-hydroxymethyl-D-glycals with phenols in trifluoroacetic acid at ambient temperature leads to an extremely facile transformation affording chiral pyrano[2,3-b]benzopyrans in high ...
Santhi, Meenakshisundaram   +2 more
core   +1 more source

Electron impact induced cyclizations in 4-chioro-3-(N-aryliminomethyl) (2H) benzopyrans and benzothiopyrans

open access: yes, 1987
Intramolecular substitutions leading to cyclizations with the ejection of chlorine have been noticed during mass spectral fragmentation of 4-chloro-3-(N-aryliminomethyl) (2H) benzopyrans and benzothiopyrans.
Balasubramanian, K. K.   +4 more
core   +1 more source

Synthesis of 3,4-Disubstituted 2H-Benzopyrans through C−C Bond Formation via Electrophilic Cyclization

open access: yes, 2016
The electrophilic cyclization of substituted propargylic aryl ethers by I2, ICl, and PhSeBr produces 3,4-disubstituted 2H-benzopyrans in excellent yields.
Tuanli Yao (1340802)   +3 more
core   +2 more sources

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