Bellemin-Laponnaz S - Search Results

1

Using a tripod as a chiral chelating ligand: chemical exchange between equivalent molecular structures in palladium catalysis with 1,1,1-tris(oxazolinyl)ethane ("trisox").

Foltz C, Enders M, Bellemin-Laponnaz S, Wadepohl H, Gade LH. Foltz C, et al. Chemistry. 2007;13(21):5994-6008. doi: 10.1002/chem.200700307. Chemistry. 2007. PMID: 17525923

2

Three 2-oxazolinyl rings on one quaternary carbon atom: preparation of a novel tripodal tris(oxazolinyl) ligand and the tetrameric molecular structure of its CuI complex.

Bellemin-Laponnaz S, Gade LH. Bellemin-Laponnaz S, et al. Chem Commun (Camb). 2002 Jun 21;(12):1286-7. doi: 10.1039/b202846h. Chem Commun (Camb). 2002. PMID: 12109118

3

A modular approach to C1 and C3 chiral N-tripodal ligands for asymmetric catalysis.

Bellemin-Laponnaz S, Gade LH. Bellemin-Laponnaz S, et al. Angew Chem Int Ed Engl. 2002 Sep 16;41(18):3473-5. doi: 10.1002/1521-3773(20020916)41:18<3473::AID-ANIE3473>3.0.CO;2-N. Angew Chem Int Ed Engl. 2002. PMID: 12298069 No abstract available.

4

A modular assembly of chiral oxazolinylcarbene-rhodium complexes: efficient phosphane-free catalysts for the asymmetric hydrosilylation of dialkyl ketones.

Gade LH, César V, Bellemin-Laponnaz S. Gade LH, et al. Angew Chem Int Ed Engl. 2004 Feb 13;43(8):1014-7. doi: 10.1002/anie.200353133. Angew Chem Int Ed Engl. 2004. PMID: 14966895 No abstract available.

5

A C3-symmetrical chiral trisoxazoline zinc complex as a functional model for zinc hydrolases: kinetic resolution of racemic chiral esters by transesterification.

Dro C, Bellemin-Laponnaz S, Welter R, Gade LH. Dro C, et al. Angew Chem Int Ed Engl. 2004 Aug 27;43(34):4479-82. doi: 10.1002/anie.200460187. Angew Chem Int Ed Engl. 2004. PMID: 15340948 No abstract available.

6

Chiral N-heterocyclic carbenes as stereodirecting ligands in asymmetric catalysis.

César V, Bellemin-Laponnaz S, Gade LH. César V, et al. Chem Soc Rev. 2004 Nov 30;33(9):619-36. doi: 10.1039/b406802p. Epub 2004 Nov 3. Chem Soc Rev. 2004. PMID: 15592627 Review.

7

C3 chirality in polymerization catalysis: a highly active dicationic scandium(III) catalyst for the isoselective polymerization of 1-hexene.

Ward BD, Bellemin-Laponnaz S, Gade LH. Ward BD, et al. Angew Chem Int Ed Engl. 2005 Mar 4;44(11):1668-71. doi: 10.1002/anie.200462804. Angew Chem Int Ed Engl. 2005. PMID: 15712251 No abstract available.

8

Designing the "search pathway" in the development of a new class of highly efficient stereoselective hydrosilylation catalysts.

César V, Bellemin-Laponnaz S, Wadepohl H, Gade LH. César V, et al. Chemistry. 2005 Apr 22;11(9):2862-73. doi: 10.1002/chem.200500132. Chemistry. 2005. PMID: 15744702

9

Exploiting C3-symmetry in the dynamic coordination of a chiral trisoxazoline to copper(II): improved enantioselectivity, and catalyst stability in asymmetric lewis acid catalysis.

Foltz C, Stecker B, Marconi G, Bellemin-Laponnaz S, Wadepohl H, Gade LH. Foltz C, et al. Chem Commun (Camb). 2005 Oct 28;(40):5115-7. doi: 10.1039/b509571a. Epub 2005 Sep 16. Chem Commun (Camb). 2005. PMID: 16220189

10

Bisoxazolines with one and two sidearms: stereodirecting ligands for copper-catalysed asymmetric allylic oxidations of alkenes.

Seitz M, Capacchione C, Bellemin-Laponnaz S, Wadepohl H, Ward BD, Gade LH. Seitz M, et al. Dalton Trans. 2006 Jan 7;(1):193-202. doi: 10.1039/b512570g. Epub 2005 Nov 14. Dalton Trans. 2006. PMID: 16357977

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