Results 281 to 290 of about 49,489 (310)
Some of the next articles are maybe not open access.
QSAR Prediction of Aquatic Toxicity of Triazoles and Benzo-Triazoles
2011Triazoles and benzo-triazoles (TAZ/BTAZ) are potentially hazardous chemicals that adversely affect humans and other non-target species, and are on the list of substances of very high concern (SVHC) in the European regulation of chemicals REACH. TAZ/BTAZ are synthetic molecules used in various industrial processes (to obtain pharmaceuticals and ...
CASSANI, STEFANO +5 more
openaire +3 more sources
2008
This chapter provides a critical update on developments in the chemistry of 1,2,4-triazoles over the last decade. 1,2,4-Triazoles have remained the topic of much research, primarily due to their ubiquitous presence in many pharmaceutical agents and, more recently, in other functional materials with uses in engineering as corrosion inhibitors and in ...
N. Jennings, Anthony D.M. Curtis
openaire +2 more sources
This chapter provides a critical update on developments in the chemistry of 1,2,4-triazoles over the last decade. 1,2,4-Triazoles have remained the topic of much research, primarily due to their ubiquitous presence in many pharmaceutical agents and, more recently, in other functional materials with uses in engineering as corrosion inhibitors and in ...
N. Jennings, Anthony D.M. Curtis
openaire +2 more sources
Synthesis of 1-(1,2,4-triazol-3-yl)-1,2,3-triazoles
Chemistry of Heterocyclic Compounds, 19801-(1,2,4-Triazol-3-yl)-1,2,3-triazoles were obtained by 1,3-dipolar cycloaddition of 3-azido-1,2,4-triazole to acetylene derivatives.
T. F. Sharamet +3 more
openaire +2 more sources
Tetrahedron Letters, 1969
Photolytic cleavage of vic-triazole ring when unsubstituted at N, finding phenylacetonitrile production ...
R. Selvarajan, J.H. Boyer
openaire +2 more sources
Photolytic cleavage of vic-triazole ring when unsubstituted at N, finding phenylacetonitrile production ...
R. Selvarajan, J.H. Boyer
openaire +2 more sources
A Recent Portrait of Bioactive Triazoles
Current Bioactive Compounds, 2010Scientists have extensively explored new synthetic routes in order to obtain 1,2,3- and 1,2,4-triazoles as they represent a very interesting class of compounds due to their wide range of biological activities such as antitumor, antiinflammatory, analgesic, antifungal, antibacterial, antiviral, etc.
PIBIRI, Ivana, BUSCEMI, Silvestre
openaire +3 more sources
Voriconazole: A second-generation triazole
Drugs of Today, 2001Voriconazole, a derivative of fluconazole, is an antifungal triazole with expanded spectrum of activity against a variety of yeasts and filamentous fungi. It exhibits fungicidal activity against Aspergillus species. Preliminary data from animal models and clinical trials show promise in the treatment of candidiasis and aspergillosis.
Elias K. Manavathu +1 more
openaire +2 more sources
Conversion of N-Sulfonyl Triazoles into Triazole-Fused Isoindolines [PDF]
Synfacts, 2019 Emma McInturff, Victor Snieckus
openaire +1 more source
Ring-Opening Coupling of Cyclopropanol with 1,2,3-Triazole for the Synthesis of Fused Triazoles
Organic LettersA radical ring-opening arylation of cyclopropanol with 1,2,3-triazole has been achieved. This synthetic protocol provides straightforward access to a wide range of structurally diverse and chiral 4,5,6,7-tetrahydro[1,2,3]triazolo[1,5-a]pyridines with high efficiency from readily available chiral cyclopropanols.
Yi Wu +8 more
openaire +2 more sources
The Chemistry of the Vicinal Triazoles.
Chemical Reviews, 1950Frederic R. Benson, Walter L. Savell
openaire +3 more sources