Benincori T - Search Results

1

Erratum to: "Inherently chiral" thiophene-based electrodes at work: a screening of enantioselection ability toward a series of pharmaceutically relevant phenolic or catecholic amino acids, amino esters, and amine.

Arnaboldi S, Benincori T, Cirilli R, Grecchi S, Santagostini L, Sannicolò F, Mussini PR. Arnaboldi S, et al. Among authors: benincori t. Anal Bioanal Chem. 2017 Feb;409(6):1717-1718. doi: 10.1007/s00216-016-0103-y. Epub 2016 Dec 27. Anal Bioanal Chem. 2017. PMID: 28028596 No abstract available.

2

2,2',5,5'-tetramethyl-4,4'-bis(diphenylphoshino)-3,3'-bithiophene: a new, very efficient, easily accessible, chiral biheteroaromatic ligand for homogeneous stereoselective catalysis.

Benincori T, Cesarotti E, Piccolo O, Sannicolo F. Benincori T, et al. J Org Chem. 2000 Apr 7;65(7):2043-7. doi: 10.1021/jo991533x. J Org Chem. 2000. PMID: 10774024

3

3,3'-Bis(diphenylphosphino)-1,1'-disubstituted-2,2'-biindoles: easily accessible, electron-rich, chiral diphosphine ligands for homogeneous enantioselective hydrogenation of oxoesters.

Benincori T, Piccolo O, Rizzo S, Sannicolo F. Benincori T, et al. J Org Chem. 2000 Dec 1;65(24):8340-7. doi: 10.1021/jo001207d. J Org Chem. 2000. PMID: 11101394

4

A new modular class of easily accessible, inexpensive, and efficient chiral diphosphine ligands for homogeneous stereoselective catalysis.

Benincori T, Gladiali S, Rizzo S, Sannicolò F. Benincori T, et al. J Org Chem. 2001 Aug 24;66(17):5940-2. doi: 10.1021/jo015738t. J Org Chem. 2001. PMID: 11511279 No abstract available.

5

Steric and electronic tuning of chiral bis(oxazoline) ligands with 3,3'-bithiophene backbone.

Benaglia M, Benincori T, Mussini P, Pilati T, Rizzo S, Sannicolò F. Benaglia M, et al. Among authors: benincori t. J Org Chem. 2005 Sep 16;70(19):7488-95. doi: 10.1021/jo050267m. J Org Chem. 2005. PMID: 16149775

6

Configurationally stable molecular propellers: the [corrected] resolution of phosphorus-centered [corrected] residual enantiomers.

Benincori T, Celentano G, Pilati T, Ponti A, Rizzo S, Sannicolò F. Benincori T, et al. Angew Chem Int Ed Engl. 2006 Sep 18;45(37):6193-6. doi: 10.1002/anie.200601869. Angew Chem Int Ed Engl. 2006. PMID: 16927445 No abstract available.

7

Spider-like oligothiophenes.

Benincori T, Capaccio M, De Angelis F, Falciola L, Muccini M, Mussini P, Ponti A, Toffanin S, Traldi P, Sannicolò F. Benincori T, et al. Chemistry. 2008;14(2):459-71. doi: 10.1002/chem.200701117. Chemistry. 2008. PMID: 18046679

8

Chirality in the absence of rigid stereogenic elements: the absolute configuration of residual enantiomers of C3-symmetric propellers.

Benincori T, Marchesi A, Mussini PR, Pilati T, Ponti A, Rizzo S, Sannicolò F. Benincori T, et al. Chemistry. 2009;15(1):86-93. doi: 10.1002/chem.200801489. Chemistry. 2009. PMID: 19053102

9

Chirality in the absence of rigid stereogenic elements: the design of configurationally stable C3-symmetric propellers.

Benincori T, Marchesi A, Pilati T, Ponti A, Rizzo S, Sannicolò F. Benincori T, et al. Chemistry. 2009;15(1):94-105. doi: 10.1002/chem.200801505. Chemistry. 2009. PMID: 19072792 Free article.

10

Towards molecular design rationalization in branched multi-thiophene semiconductors: the 2-thienyl-persubstituted alpha-oligothiophenes.

Benincori T, Bonometti V, De Angelis F, Falciola L, Muccini M, Mussini PR, Pilati T, Rampinini G, Rizzo S, Toffanin S, Sannicolò F. Benincori T, et al. Chemistry. 2010 Aug 9;16(30):9086-98. doi: 10.1002/chem.200903546. Chemistry. 2010. PMID: 20583047

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