
![]() |
|||||||||||||
WJPR Citation
|
| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
INTERMOLECULAR DOMINO MICHAEL-[3+2] CYCLOADDITION THREE-COMPONENT COUPLING REACTIONS: A NEW SYNTHESIS OF 1, 5-DISUSTITUTED TETRAZOLES
Yugandhar Kothapalli, Sridhar Musulla, Mahesh Madala and Srinivasa Rao Alapati*
Abstract Intermolecular domino Michael-[3+2] cyclo addition reaction is described. Initial azide addition in a Michael fashion to acetylated Baylis-Hillman adducts and followed by reacted with p-toluene sulfonyl nitrile give multifunctional 1,5-disubstituted 1,2,3,4- tetrazoles. Keywords: Three-component coupling reaction, Baylis Hillman adducts, tetrazoles, p-toluene sulfonylnitrile [Full Text Article] [Download Certificate] |
