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Cationic palladium(II)-catalyzed highly enantioselective [3+2] annulation of 2-acylarylboronic acids with substituted alkynes.
Org Lett. 2007 Nov 22; 9(24):5131-3.OL

Abstract

A cationic palladium(II)-catalyzed enantioselective tandem [3+2] annulation of 2-acylarylboronic acids with substituted alkynes to yield optically active 1-indenols was developed in high yields and excellent enantioselectivities.

Authors+Show Affiliations

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Science, 354 Fenglin Road, Shanghai 200032, China.No affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

17975925

Citation

Yang, Miao, et al. "Cationic palladium(II)-catalyzed Highly Enantioselective [3+2] Annulation of 2-acylarylboronic Acids With Substituted Alkynes." Organic Letters, vol. 9, no. 24, 2007, pp. 5131-3.
Yang M, Zhang X, Lu X. Cationic palladium(II)-catalyzed highly enantioselective [3+2] annulation of 2-acylarylboronic acids with substituted alkynes. Org Lett. 2007;9(24):5131-3.
Yang, M., Zhang, X., & Lu, X. (2007). Cationic palladium(II)-catalyzed highly enantioselective [3+2] annulation of 2-acylarylboronic acids with substituted alkynes. Organic Letters, 9(24), 5131-3.
Yang M, Zhang X, Lu X. Cationic palladium(II)-catalyzed Highly Enantioselective [3+2] Annulation of 2-acylarylboronic Acids With Substituted Alkynes. Org Lett. 2007 Nov 22;9(24):5131-3. PubMed PMID: 17975925.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Cationic palladium(II)-catalyzed highly enantioselective [3+2] annulation of 2-acylarylboronic acids with substituted alkynes. AU - Yang,Miao, AU - Zhang,Xumu, AU - Lu,Xiyan, Y1 - 2007/11/02/ PY - 2007/11/3/pubmed PY - 2008/1/26/medline PY - 2007/11/3/entrez SP - 5131 EP - 3 JF - Organic letters JO - Org Lett VL - 9 IS - 24 N2 - A cationic palladium(II)-catalyzed enantioselective tandem [3+2] annulation of 2-acylarylboronic acids with substituted alkynes to yield optically active 1-indenols was developed in high yields and excellent enantioselectivities. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/17975925/Cationic_palladium_II__catalyzed_highly_enantioselective_[3+2]_annulation_of_2_acylarylboronic_acids_with_substituted_alkynes_ L2 - https://doi.org/10.1021/ol702503e DB - PRIME DP - Unbound Medicine ER -