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Volumn 66, Issue 15, 2001, Pages 5266-5268

A straightforward synthetic entry to the 4,9b-propanopyrrolo[2,3-c]quinoline system by a new reductive cyclization of α′-(2-nitrophenyl) enones

(4) Sole D a Garcia Rubio S a,b Vallverdu L a Bonjoch, J a

a UNIVERSITY OF BARCELONA (Spain)

b Albany Molecular Research (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; ALPHA (2 NITROPHENYL) ENONE; CARBON; KETONE DERIVATIVE; NITROGEN; QUINOLINE DERIVATIVE; TETRAHYDROQUINOLINE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CYCLIZATION; REDUCTION; SYNTHESIS;

CYCLIZATION; HYDROGEN-ION CONCENTRATION; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION-REDUCTION; PYRROLES; QUINOLINES; SPECTROPHOTOMETRY, INFRARED; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 0035958490 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo015659h Document Type: Article

Times cited : (11)

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