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Palladium-catalyzed α-arylation of sultams with aryl and heteroaryl iodides.
Org Lett. 2014 Jul 03; 16(13):3468-71.OL

Abstract

Palladium(0)-catalyzed conditions for the α-arylation of sultams with aryl and heteroaryl iodides have been developed. Arylation of 3-substituted 1,3-propanesultams gave rise to high yields and high diastereomeric ratios, leading to the thermodynamically favored cis product. The arylation was broadly applicable to various electron-rich and electron-poor (hetero)aromatic iodides.

Authors+Show Affiliations

Discovery Chemistry and ‡Small Molecule Process Chemistry, Genentech, Inc. , 1 DNA Way, South San Francisco, California 94080, United States.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

24937120

Citation

René, Olivier, et al. "Palladium-catalyzed Α-arylation of Sultams With Aryl and Heteroaryl Iodides." Organic Letters, vol. 16, no. 13, 2014, pp. 3468-71.
René O, Fauber BP, Malhotra S, et al. Palladium-catalyzed α-arylation of sultams with aryl and heteroaryl iodides. Org Lett. 2014;16(13):3468-71.
René, O., Fauber, B. P., Malhotra, S., & Yajima, H. (2014). Palladium-catalyzed α-arylation of sultams with aryl and heteroaryl iodides. Organic Letters, 16(13), 3468-71. https://doi.org/10.1021/ol501389k
René O, et al. Palladium-catalyzed Α-arylation of Sultams With Aryl and Heteroaryl Iodides. Org Lett. 2014 Jul 3;16(13):3468-71. PubMed PMID: 24937120.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Palladium-catalyzed α-arylation of sultams with aryl and heteroaryl iodides. AU - René,Olivier, AU - Fauber,Benjamin P, AU - Malhotra,Sushant, AU - Yajima,Herbert, Y1 - 2014/06/17/ PY - 2014/6/18/entrez PY - 2014/6/18/pubmed PY - 2014/9/3/medline SP - 3468 EP - 71 JF - Organic letters JO - Org Lett VL - 16 IS - 13 N2 - Palladium(0)-catalyzed conditions for the α-arylation of sultams with aryl and heteroaryl iodides have been developed. Arylation of 3-substituted 1,3-propanesultams gave rise to high yields and high diastereomeric ratios, leading to the thermodynamically favored cis product. The arylation was broadly applicable to various electron-rich and electron-poor (hetero)aromatic iodides. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/24937120/Palladium_catalyzed_α_arylation_of_sultams_with_aryl_and_heteroaryl_iodides_ DB - PRIME DP - Unbound Medicine ER -