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|Title:||Addition of indoles to oxyallyl cations for facile access to α-indole carbonyl compounds||Authors:||Tang, Qiang
Chi, Robin Yonggui
|Issue Date:||2012||Source:||Tang, Q., Chen, X., Tiwari, B., & Chi, Y. R. (2012). Addition of Indoles to Oxyallyl Cations for Facile Access to α-Indole Carbonyl Compounds. Organic Letters, 14(7), 1922-1925.||Series/Report no.:||Organic letters||Abstract:||A direct coupling of unprotected indoles and α-halo ketones via in situ generated oxyallyl cation intermediates is described. The reactions efficiently afford α-indole carbonyl compounds with good to quantitative yields.||URI:||https://hdl.handle.net/10356/97259
|ISSN:||1523-7060||DOI:||10.1021/ol300591z||Rights:||© 2012 American Chemical Society.||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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