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.
Links
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 -