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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

Yang M
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Science, 354 Fenglin Road, Shanghai 200032, China.
Zhang X
No affiliation info available
Lu X
No affiliation info available

MeSH

AlkynesBoronic AcidsCatalysisCationsCyclizationIndenesMolecular StructureOrganometallic CompoundsPalladiumStereoisomerism

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_ DB - PRIME DP - Unbound Medicine ER -