Publication year: 2012 Source: Tetrahedron Letters, Available online 20 January 2012 Junali Gogoi, Pranjal Bezbaruah, Pallabi Saikia, Junali Goswami, Pranjal Gogoi, … A facile synthesis of a novel class of steroidal A/B/D-ring annulated tetrazolo[1,5-a]pyridine derivatives has been accomplishedviaintramolecular 1,3-dipolar cycloaddition reaction of azide with nitrile in aprotic solvent. The synthesis of D-ring annulated tetrazolo[1,5-a]pyridine in alcohol showed incorporation of an alcohol molecule into heterocyclic system
Continue Reading:
Synthesis of a novel class of steroidal tetrazolo[1,5-a]pyridinesviaintramolecular 1,3-dipolar cycloadditions
Related posts:
- Isocyanide-based four-component synthesis of ferrocenyl 1,5-disubstituted tetrazoles
- A versatile approach to the regioselective synthesis of diverse (-)-epicatechin- β -D-glucuronides
- An efficient synthesis of the 4’-epimer of 2-fluoronoraristeromycin
- Biyoulactones D and E, meroterpenoids fromHypericum chinense
- First synthesis of 1-(indol-2-yl)azulenes by the Vilsmeier-Haack type arylation with triflic anhydride as an activating reagent
- Synthesis of 1-aryl-substituted-4-chloroimidazo[1,2-a]quinoxalines catalyzed by PdCl2in water
- Agricultural waste in the Synthesis of Coral Ceramic Pigment
- Non-cyclic class groups and the Brumer–Stark conjecture
- Preparation of nanostructured nickel aluminate spinel powder from spent NiO/Al2O3catalyst by mechano-chemical synthesis
- A general class of zero-or-one inflated beta regression models
