Synthesis Of Poly Functionalized Tricyclic Nitro Chromenopyrazole Frameworks Via Intramolecular Cycloaddition Reactio Derived From Nitroolefins
DOI:
https://doi.org/10.64252/b211c614Keywords:
Baylis-Hillman adducts, Chromenopyrazole and O-allylated salicylaldehyde, (E)-2-nitro-3-phenylprop-2- en-1-ol, Conc. HCl and ethanol.Abstract
A simple and novel protocol for the easy synthesis of complex angle-substituted tricyclic frameworks including the IA 3a-nitro2,3 diphenyl-2,3a,4-tetrahydrochromeno[4.3-C]pyrazole ring system. This reaction leads to a new class of merged merges and tetra cycles, creating two new rings, three coherent steer centers and a carbon center that replaces tetras in a unique way. The angle-substituted nitro compounds were highly stereoselectively conserved in high yields
Downloads
Download data is not yet available.
Downloads
Published
2025-06-18
Issue
Section
Articles
How to Cite
Synthesis Of Poly Functionalized Tricyclic Nitro Chromenopyrazole Frameworks Via Intramolecular Cycloaddition Reactio Derived From Nitroolefins. (2025). International Journal of Environmental Sciences, 1460-1465. https://doi.org/10.64252/b211c614