Journal
ORGANIC LETTERS
Volume 20, Issue 1, Pages 220-223Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b03580
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Funding
- Thousand Youth Talents Plan, NSFC [21672145, 51733007]
- Shuguang program from SEDF [16SG10]
- Shuguang program from SMEC [16SG10]
- Shuguang program from STCSM [17JC1403700]
- Innovation Fund from Shanghai Jiao Tong University [IFPM016A002]
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An efficient and environmentally benign Cu-mediated method was developed for direct cascade C-H/N-H annulation to construct polyheterocyclic indoloquinoline scaffolds. This method highlights an emerging strategy for transforming inert C-H bonds into versatile functional groups in organic synthesis and provides a new versatile approach for the efficient synthesis of indolo [3,2-c] and [2,3-c] quinoline alkaloids.
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