Asymmetric 1,4-Reduction of Pyrano[2,3-b]indoles with Hantzsch Ester by Chiral Phosphoric Acid
Author:
Affiliation:
1. Key Laboratory of Optic-electric Sensing and Analytic Chemistry for Life Science, MOE, College of Chemistry and Molecular Engineering, Qingdao University of Science & Technology, Qingdao 255042, China
Funder
Qingdao University of Science and Technology
Taishan Scholar Project of Shandong Province
Natural Science Foundation of Shandong Province
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02385
Reference18 articles.
1. Structure-optimized dihydropyranoindole derivative GIBH-LRA002 potentially reactivated viral latency in primary CD4+ T lymphocytes of chronic HIV-1 patients
2. Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted chromeno[2,3-b]indoles
3. cYang, K.; Li, J.; Li, Q.; Leng, H.; Shen, X.; Liu, Y.; Zhu, H.; Lai, H.; Zhang, X.; Dai, Q.; Liu, Y.; Zeng, R.; Zhang, Y. Process for Preparation of Tetrahydropyran[2,3-b]indole Skeleton Compound. Patent CN108047237A, 2018.
4. Microwave assisted synthesis of indole-annulated dihydropyrano[3,4-c]chromene derivatives via hetero-Diels–Alder reaction
5. Organocatalytic Enantioselective Synthesis of Dihydropyrano- indole Derivatives Bearing Trifluoromethylated All-Carbon- Substituted Stereocenters
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