Tags

Type your tag names separated by a space and hit enter

Pd-Catalyzed C-H Functionalization of Indole-Containing Alkene-Tethered Aryl Halides with Alkynes To Construct Indole Alkaloid Scaffolds.
Org Lett. 2022 04 22; 24(15):2910-2914.OL

Abstract

A convenient and straightforward approach for the construction of indole alkaloid scaffolds from indole-containing alkene-tethered aryl halides and alkynes through a sequential C-H activation, five-membered palladacycle formation, and alkyne insertion process has been described. The approach provides a series of indole alkaloid compounds in moderate to excellent yields with good functional tolerance.

Authors+Show Affiliations

Inner Mongolia Key Laboratory of Fine Organic Synthesis, Department of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.Inner Mongolia Key Laboratory of Fine Organic Synthesis, Department of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.Inner Mongolia Key Laboratory of Fine Organic Synthesis, Department of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

35394792

Citation

Qi, Hongbo, et al. "Pd-Catalyzed C-H Functionalization of Indole-Containing Alkene-Tethered Aryl Halides With Alkynes to Construct Indole Alkaloid Scaffolds." Organic Letters, vol. 24, no. 15, 2022, pp. 2910-2914.
Qi H, Chi D, Chen S. Pd-Catalyzed C-H Functionalization of Indole-Containing Alkene-Tethered Aryl Halides with Alkynes To Construct Indole Alkaloid Scaffolds. Org Lett. 2022;24(15):2910-2914.
Qi, H., Chi, D., & Chen, S. (2022). Pd-Catalyzed C-H Functionalization of Indole-Containing Alkene-Tethered Aryl Halides with Alkynes To Construct Indole Alkaloid Scaffolds. Organic Letters, 24(15), 2910-2914. https://doi.org/10.1021/acs.orglett.2c00882
Qi H, Chi D, Chen S. Pd-Catalyzed C-H Functionalization of Indole-Containing Alkene-Tethered Aryl Halides With Alkynes to Construct Indole Alkaloid Scaffolds. Org Lett. 2022 04 22;24(15):2910-2914. PubMed PMID: 35394792.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Pd-Catalyzed C-H Functionalization of Indole-Containing Alkene-Tethered Aryl Halides with Alkynes To Construct Indole Alkaloid Scaffolds. AU - Qi,Hongbo, AU - Chi,Dongmei, AU - Chen,Shufeng, Y1 - 2022/04/08/ PY - 2022/4/9/pubmed PY - 2022/4/26/medline PY - 2022/4/8/entrez SP - 2910 EP - 2914 JF - Organic letters JO - Org Lett VL - 24 IS - 15 N2 - A convenient and straightforward approach for the construction of indole alkaloid scaffolds from indole-containing alkene-tethered aryl halides and alkynes through a sequential C-H activation, five-membered palladacycle formation, and alkyne insertion process has been described. The approach provides a series of indole alkaloid compounds in moderate to excellent yields with good functional tolerance. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/35394792/Pd_Catalyzed_C_H_Functionalization_of_Indole_Containing_Alkene_Tethered_Aryl_Halides_with_Alkynes_To_Construct_Indole_Alkaloid_Scaffolds_ DB - PRIME DP - Unbound Medicine ER -