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Copper-Catalyzed Annulation Cascades of Alkyne-Tethered α-Bromocarbonyls with Alkynes: An Access to Heteropolycycles.

Authors :
Liu B
Yu JX
Li Y
Li JH
He DL
Source :
Organic letters [Org Lett] 2018 Apr 20; Vol. 20 (8), pp. 2129-2132. Date of Electronic Publication: 2018 Mar 29.
Publication Year :
2018

Abstract

We here describe a new Cu-catalyzed annulation cascade of alkyne-tethered α-bromocarbonyls with common alkynes for the synthesis of various heteropolycycle frameworks, including 1 H-benzo[ de]quinolin-2(3 H)-ones, 4 H-dibenzo[ de,g]quinolin-5(6 H)-one, and benzo[ de]chromen-2(3 H)-one, which were constructed with high selectivity. This was achieved by two-component annulation cascades, rather than atom-transfer radical cyclization (ATRC), with alkyne-tethered α-bromocarbonyls for one-step accessing heteropolycycles via C-Br bond split, intramolecular cyclization, intermolecular [4 + 2] annulation, and aryl C(sp <superscript>2</superscript> )-H functionalization cascades.

Details

Language :
English
ISSN :
1523-7052
Volume :
20
Issue :
8
Database :
MEDLINE
Journal :
Organic letters
Publication Type :
Academic Journal
Accession number :
29595989
Full Text :
https://doi.org/10.1021/acs.orglett.8b00236