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Development of chiral terminal-alkene-phosphine hybrid ligands for palladium-catalyzed asymmetric allylic substitutions.
Org Lett. 2010 Jul 02; 12(13):3054-7.OL

Abstract

A variety of novel chiral terminal-alkene-phosphine hybrid ligands were successfully developed from diethyl L-tartrate for palladium-catalyzed asymmetric allylic alkylations, etherifications, and amination to give the desired products in excellent yields and ee's.

Authors+Show Affiliations

Beijing National Laboratory of Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.No affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

20536224

Citation

Liu, Zhaoqun, and Haifeng Du. "Development of Chiral Terminal-alkene-phosphine Hybrid Ligands for Palladium-catalyzed Asymmetric Allylic Substitutions." Organic Letters, vol. 12, no. 13, 2010, pp. 3054-7.
Liu Z, Du H. Development of chiral terminal-alkene-phosphine hybrid ligands for palladium-catalyzed asymmetric allylic substitutions. Org Lett. 2010;12(13):3054-7.
Liu, Z., & Du, H. (2010). Development of chiral terminal-alkene-phosphine hybrid ligands for palladium-catalyzed asymmetric allylic substitutions. Organic Letters, 12(13), 3054-7. https://doi.org/10.1021/ol101069y
Liu Z, Du H. Development of Chiral Terminal-alkene-phosphine Hybrid Ligands for Palladium-catalyzed Asymmetric Allylic Substitutions. Org Lett. 2010 Jul 2;12(13):3054-7. PubMed PMID: 20536224.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Development of chiral terminal-alkene-phosphine hybrid ligands for palladium-catalyzed asymmetric allylic substitutions. AU - Liu,Zhaoqun, AU - Du,Haifeng, PY - 2010/6/12/entrez PY - 2010/6/12/pubmed PY - 2010/9/21/medline SP - 3054 EP - 7 JF - Organic letters JO - Org Lett VL - 12 IS - 13 N2 - A variety of novel chiral terminal-alkene-phosphine hybrid ligands were successfully developed from diethyl L-tartrate for palladium-catalyzed asymmetric allylic alkylations, etherifications, and amination to give the desired products in excellent yields and ee's. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/20536224/Development_of_chiral_terminal_alkene_phosphine_hybrid_ligands_for_palladium_catalyzed_asymmetric_allylic_substitutions_ DB - PRIME DP - Unbound Medicine ER -