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Convenient synthesis of antiproliferative 2,3-dihydro-2,3′-bisindoles via dimerization of N-H indole derivatives
[Display omitted] A convenient and efficient approach for the synthesis of 2,3-dihydro-2,3′-bisindoles has been developed in good yields via dimerization of N-H indole derivatives. The synthetic utility of this approach was demonstrated by the rapid construction of bisindoles in gram-scale. Biologic...
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Published in: | Tetrahedron letters 2016-03, Vol.57 (10), p.1097-1099 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
A convenient and efficient approach for the synthesis of 2,3-dihydro-2,3′-bisindoles has been developed in good yields via dimerization of N-H indole derivatives. The synthetic utility of this approach was demonstrated by the rapid construction of bisindoles in gram-scale. Biological evaluation revealed that some of the obtained 2,3-dihydro-2,3′-bisindoles exhibited significant in vitro antiproliferative activities on human-derived lung, liver, stomach, and breast cancer cell lines. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2016.01.093 |