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https://hdl.handle.net/10356/99426
Title: | Silver triflate catalyzed tandem heterocyclization/alkynylation of 1-((2-tosylamino)aryl)but-2-yne-1,4-diols to 2-alkynyl indoles | Authors: | Mothe, Srinivasa Reddy Kothandaraman, Prasath Lauw, Sherman Jun Liang Chin, Samuel Ming Wei Chan, Philip Wai Hong |
Issue Date: | 2012 | Source: | Mothe, S. R., Kothandaraman, P., Lauw, S. J. L., Chin, S. M. W.,& Chan, P. W. H. (2012). Silver Triflate Catalyzed Tandem Heterocyclization/Alkynylation of 1-((2-Tosylamino)aryl)but-2-yne-1,4-diols to 2-Alkynyl Indoles. Chemistry - A European Journal, 18(20), 6133-6137. | Series/Report no.: | Chemistry - a European journal | Abstract: | Don't cross me! 2-Alkynyl indoles were prepared efficiently by the AgOTf-catalyzed tandem heterocyclization/alkynylation of 1-(2-tosylamino)aryl)but-2-yne-1,4-diols under mild conditions (see scheme). The attractiveness of this approach lies in the fact that both the indole ring and alkyne side chain of the N-heterocycle are sequentially formed from low cost, readily available, and ecologically benign starting materials. It also provides the first route to this synthetically valuable class of compounds that is not based on a cross-coupling strategy. | URI: | https://hdl.handle.net/10356/99426 http://hdl.handle.net/10220/12940 |
ISSN: | 0947-6539 | DOI: | 10.1002/chem.201200578 | Schools: | School of Physical and Mathematical Sciences | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SPMS Journal Articles |
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