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The preparation of 4,5-dihydro-2H-benz[e]indazoles from dilithiated 2-tetralone phenylhydrazone and aromatic esters

✍ Scribed by April J. Angel; Anne E. Finefrock; Angela R. Williams; Jessica D. Townsend; Thuy-Ha V. Nguyen; Douglas R. Hurst; Frederick J. Heldrich; Charles F. Beam; Ibraheem T. Badejo


Publisher
Journal of Heterocyclic Chemistry
Year
1999
Tongue
English
Weight
270 KB
Volume
36
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

The phenylhydrazone of 2‐tetralone was dilithiated with excess lithium diisopropylamide followed by condensation with several aromatic esters, and the resulting intermediates were acid cyclized to 4,5‐dihydro‐2__H__‐benz[e]indazoles.


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