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Cationic palladium(II)-catalyzed highly enantioselective tandem reactions of ortho-boronate-substituted cinnamic ketones and internal alkynes: a convenient synthesis of optically active indenes.
Org Lett. 2009 Mar 19; 11(6):1405-8.OL

Abstract

Cationic palladium(II)-catalyzed tandem reactions of ortho-boronate-substituted cinnamic ketones and internal alkynes to yield optically active indenes were developed in high yields and good enantioselectivities.

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Publisher Full Text (DOI)

Authors+Show Affiliations

Zhou F
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Science, 345 Lingling Road, Shanghai 200032, China.
Yang M
No affiliation info available
Lu X
No affiliation info available

MeSH

AlkynesBoronic AcidsCinnamatesCombinatorial Chemistry TechniquesIndenesKetonesMolecular StructurePalladiumStereoisomerism

Pub Type(s)

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

Language

eng

PubMed ID

19243157

Citation

Zhou, Feng, et al. "Cationic palladium(II)-catalyzed Highly Enantioselective Tandem Reactions of Ortho-boronate-substituted Cinnamic Ketones and Internal Alkynes: a Convenient Synthesis of Optically Active Indenes." Organic Letters, vol. 11, no. 6, 2009, pp. 1405-8.
Zhou F, Yang M, Lu X. Cationic palladium(II)-catalyzed highly enantioselective tandem reactions of ortho-boronate-substituted cinnamic ketones and internal alkynes: a convenient synthesis of optically active indenes. Org Lett. 2009;11(6):1405-8.
Zhou, F., Yang, M., & Lu, X. (2009). Cationic palladium(II)-catalyzed highly enantioselective tandem reactions of ortho-boronate-substituted cinnamic ketones and internal alkynes: a convenient synthesis of optically active indenes. Organic Letters, 11(6), 1405-8. https://doi.org/10.1021/ol9001015
Zhou F, Yang M, Lu X. Cationic palladium(II)-catalyzed Highly Enantioselective Tandem Reactions of Ortho-boronate-substituted Cinnamic Ketones and Internal Alkynes: a Convenient Synthesis of Optically Active Indenes. Org Lett. 2009 Mar 19;11(6):1405-8. PubMed PMID: 19243157.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Cationic palladium(II)-catalyzed highly enantioselective tandem reactions of ortho-boronate-substituted cinnamic ketones and internal alkynes: a convenient synthesis of optically active indenes. AU - Zhou,Feng, AU - Yang,Miao, AU - Lu,Xiyan, PY - 2009/2/27/entrez PY - 2009/2/27/pubmed PY - 2009/4/10/medline SP - 1405 EP - 8 JF - Organic letters JO - Org Lett VL - 11 IS - 6 N2 - Cationic palladium(II)-catalyzed tandem reactions of ortho-boronate-substituted cinnamic ketones and internal alkynes to yield optically active indenes were developed in high yields and good enantioselectivities. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/19243157/Cationic_palladium_II__catalyzed_highly_enantioselective_tandem_reactions_of_ortho_boronate_substituted_cinnamic_ketones_and_internal_alkynes:_a_convenient_synthesis_of_optically_active_indenes_ L2 - https://doi.org/10.1021/ol9001015 DB - PRIME DP - Unbound Medicine ER -