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Bidentate NHC-based chiral ligands for efficient Cu-catalyzed enantioselective allylic alkylations: structure and activity of an air-stable chiral Cu complex.
J Am Chem Soc. 2004 Sep 15; 126(36):11130-1.JA

Abstract

Cu-catalyzed addition of alkylzinc reagents to a range of allylic phosphates is promoted efficiently and with high enantioselectivity to afford tertiary as well as quaternary carbon centers (up to 98% ee). Reactions proceed to completion with 0.5-5 mol % catalyst loading and are best promoted by commercially available CuCl2.2H2O. The X-ray structure of the chiral NHC-Ag(I) complex used in the study as well as that of a catalytically active NHC-Cu(II) complex are also reported; both complexes are air-stable and are formed in >/=95% isolated yield. The isolated Cu complex, which can be handled in air, is catalytically active. The present report provides the first precedent for efficient Cu-catalyzed allylic alkylations with chiral NHC ligands.

Authors+Show Affiliations

Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

15355076

Citation

Larsen, Andrew O., et al. "Bidentate NHC-based Chiral Ligands for Efficient Cu-catalyzed Enantioselective Allylic Alkylations: Structure and Activity of an Air-stable Chiral Cu Complex." Journal of the American Chemical Society, vol. 126, no. 36, 2004, pp. 11130-1.
Larsen AO, Leu W, Oberhuber CN, et al. Bidentate NHC-based chiral ligands for efficient Cu-catalyzed enantioselective allylic alkylations: structure and activity of an air-stable chiral Cu complex. J Am Chem Soc. 2004;126(36):11130-1.
Larsen, A. O., Leu, W., Oberhuber, C. N., Campbell, J. E., & Hoveyda, A. H. (2004). Bidentate NHC-based chiral ligands for efficient Cu-catalyzed enantioselective allylic alkylations: structure and activity of an air-stable chiral Cu complex. Journal of the American Chemical Society, 126(36), 11130-1.
Larsen AO, et al. Bidentate NHC-based Chiral Ligands for Efficient Cu-catalyzed Enantioselective Allylic Alkylations: Structure and Activity of an Air-stable Chiral Cu Complex. J Am Chem Soc. 2004 Sep 15;126(36):11130-1. PubMed PMID: 15355076.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Bidentate NHC-based chiral ligands for efficient Cu-catalyzed enantioselective allylic alkylations: structure and activity of an air-stable chiral Cu complex. AU - Larsen,Andrew O, AU - Leu,Wenhao, AU - Oberhuber,Christina Nieto, AU - Campbell,John E, AU - Hoveyda,Amir H, PY - 2004/9/10/pubmed PY - 2005/4/21/medline PY - 2004/9/10/entrez SP - 11130 EP - 1 JF - Journal of the American Chemical Society JO - J Am Chem Soc VL - 126 IS - 36 N2 - Cu-catalyzed addition of alkylzinc reagents to a range of allylic phosphates is promoted efficiently and with high enantioselectivity to afford tertiary as well as quaternary carbon centers (up to 98% ee). Reactions proceed to completion with 0.5-5 mol % catalyst loading and are best promoted by commercially available CuCl2.2H2O. The X-ray structure of the chiral NHC-Ag(I) complex used in the study as well as that of a catalytically active NHC-Cu(II) complex are also reported; both complexes are air-stable and are formed in >/=95% isolated yield. The isolated Cu complex, which can be handled in air, is catalytically active. The present report provides the first precedent for efficient Cu-catalyzed allylic alkylations with chiral NHC ligands. SN - 0002-7863 UR - https://www.unboundmedicine.com/medline/citation/15355076/Bidentate_NHC_based_chiral_ligands_for_efficient_Cu_catalyzed_enantioselective_allylic_alkylations:_structure_and_activity_of_an_air_stable_chiral_Cu_complex_ DB - PRIME DP - Unbound Medicine ER -