Synthesis of Indoles through Palladium-Catalyzed Three-Component Reaction of Aryl Iodides, Alkynes, and Diaziridinone.Org Lett. 2018 10 19; 20(20):6440-6443.OL
Abstract
The three-component reaction of aryl iodides, alkynes, and diaziridinone is described. The reaction provides an innovative synthetic approach for indoles. The approach features high efficiency, broad substrate scope, and excellent regioselectivity. C, C-Palladacycles should act as the intermediates. The C, C-palladacycles are obtained from simple aryl halides and alkynes and then reacted with diaziridinone to afford indoles.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
30336674
Citation
Zhou, Bo, et al. "Synthesis of Indoles Through Palladium-Catalyzed Three-Component Reaction of Aryl Iodides, Alkynes, and Diaziridinone." Organic Letters, vol. 20, no. 20, 2018, pp. 6440-6443.
Zhou B, Wu Z, Ma D, et al. Synthesis of Indoles through Palladium-Catalyzed Three-Component Reaction of Aryl Iodides, Alkynes, and Diaziridinone. Org Lett. 2018;20(20):6440-6443.
Zhou, B., Wu, Z., Ma, D., Ji, X., & Zhang, Y. (2018). Synthesis of Indoles through Palladium-Catalyzed Three-Component Reaction of Aryl Iodides, Alkynes, and Diaziridinone. Organic Letters, 20(20), 6440-6443. https://doi.org/10.1021/acs.orglett.8b02750
Zhou B, et al. Synthesis of Indoles Through Palladium-Catalyzed Three-Component Reaction of Aryl Iodides, Alkynes, and Diaziridinone. Org Lett. 2018 10 19;20(20):6440-6443. PubMed PMID: 30336674.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Synthesis of Indoles through Palladium-Catalyzed Three-Component Reaction of Aryl Iodides, Alkynes, and Diaziridinone.
AU - Zhou,Bo,
AU - Wu,Zhuo,
AU - Ma,Ding,
AU - Ji,Xiaoming,
AU - Zhang,Yanghui,
Y1 - 2018/10/10/
PY - 2018/10/20/entrez
PY - 2018/10/20/pubmed
PY - 2018/10/20/medline
SP - 6440
EP - 6443
JF - Organic letters
JO - Org Lett
VL - 20
IS - 20
N2 - The three-component reaction of aryl iodides, alkynes, and diaziridinone is described. The reaction provides an innovative synthetic approach for indoles. The approach features high efficiency, broad substrate scope, and excellent regioselectivity. C, C-Palladacycles should act as the intermediates. The C, C-palladacycles are obtained from simple aryl halides and alkynes and then reacted with diaziridinone to afford indoles.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/30336674/Synthesis_of_Indoles_through_Palladium_Catalyzed_Three_Component_Reaction_of_Aryl_Iodides_Alkynes_and_Diaziridinone_
DB - PRIME
DP - Unbound Medicine
ER -