Synthesis Of Poly Functionalized Tricyclic Nitro Chromenopyrazole Frameworks Via Intramolecular Cycloaddition Reactio Derived From Nitroolefins

Authors

  • Senthil Author
  • D. Sujatha Krishna Author
  • K. Rajesh Author
  • N. Sivakumar Author

DOI:

https://doi.org/10.64252/b211c614

Keywords:

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

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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