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Cationic palladium complex catalyzed diastereo- and enantioselective tandem annulation of 2-formylarylboronic acids with allenoates.
Org Lett. 2009 Oct 01; 11(19):4366-9.OL

Abstract

Cationic palladium complex [(dppp)Pd(H(2)O)(2)](2+)(BF(4)(-))(2) catalyzed tandem annulation reactions of 2-formylarylboronic acids and allenoates produce the indenol derivatives diastereo- and enantioselectively in a highly efficient way.

Authors+Show Affiliations

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, China.No affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

19719091

Citation

Yu, Xufen, and Xiyan Lu. "Cationic Palladium Complex Catalyzed Diastereo- and Enantioselective Tandem Annulation of 2-formylarylboronic Acids With Allenoates." Organic Letters, vol. 11, no. 19, 2009, pp. 4366-9.
Yu X, Lu X. Cationic palladium complex catalyzed diastereo- and enantioselective tandem annulation of 2-formylarylboronic acids with allenoates. Org Lett. 2009;11(19):4366-9.
Yu, X., & Lu, X. (2009). Cationic palladium complex catalyzed diastereo- and enantioselective tandem annulation of 2-formylarylboronic acids with allenoates. Organic Letters, 11(19), 4366-9. https://doi.org/10.1021/ol901714d
Yu X, Lu X. Cationic Palladium Complex Catalyzed Diastereo- and Enantioselective Tandem Annulation of 2-formylarylboronic Acids With Allenoates. Org Lett. 2009 Oct 1;11(19):4366-9. PubMed PMID: 19719091.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Cationic palladium complex catalyzed diastereo- and enantioselective tandem annulation of 2-formylarylboronic acids with allenoates. AU - Yu,Xufen, AU - Lu,Xiyan, PY - 2009/9/2/entrez PY - 2009/9/2/pubmed PY - 2009/12/16/medline SP - 4366 EP - 9 JF - Organic letters JO - Org Lett VL - 11 IS - 19 N2 - Cationic palladium complex [(dppp)Pd(H(2)O)(2)](2+)(BF(4)(-))(2) catalyzed tandem annulation reactions of 2-formylarylboronic acids and allenoates produce the indenol derivatives diastereo- and enantioselectively in a highly efficient way. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/19719091/Cationic_palladium_complex_catalyzed_diastereo__and_enantioselective_tandem_annulation_of_2_formylarylboronic_acids_with_allenoates_ L2 - https://doi.org/10.1021/ol901714d DB - PRIME DP - Unbound Medicine ER -