Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/97259
Title: Addition of indoles to oxyallyl cations for facile access to α-indole carbonyl compounds
Authors: Tang, Qiang
Chen, Xingkuan
Tiwari, Bhoopendra
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
http://hdl.handle.net/10220/10633
ISSN: 1523-7060
DOI: http://dx.doi.org/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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