Microwave-assisted multicomponent reactions: rapid and regioselective formation of new extended angular fused aza-heterocycles.

Abstract:

:A new multicomponent domino reaction for rapid and regioselective synthesis of highly functionalized benzo[h]naphtho[2,3-a]acridine-15,16(5H,14H)-diones has been established. The reaction can be conducted by using readily available and inexpensive substrates under microwave irradiation. The procedures are facile, avoiding timeconsuming and costly syntheses, tedious work-up and purifications of precursors as well as protection/deprotection of functional groups. This method is much more efficient due to short reaction times and easy work up. The resulting naphthoacridines have been readily converted into benzoquinoxaline-fused benzoquinoline analogues by treating with benzene-1,2-diamine under microwave irradiation. The structural assignment has been ambiguously confirmed by X-ray analysis. A new mechanism has been proposed for this new multicomponent domino process.

authors

Wang SL,Zhang G,Jie D,Jiang B,Wang XH,Tu SJ

doi

10.2174/138620712800194459

subject

Has Abstract

pub_date

2012-06-01 00:00:00

pages

400-10

issue

5

eissn

1386-2073

issn

1875-5402

pii

CCHTS-EPUB-20120119-011

journal_volume

15

pub_type

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