New enantiomerically pure plienanthroline- and bipyridine-containing macrocycles have been synthesized by combination of the coordinating unit to inexpensive and readily available chiral templates. The catalytic properties of their Cu(I) complexes have been Studied in the cyclopropanation of alkenes as test reaction. A simple structural modification of the chiral cavity allowed us to successfully control the trans or cis diastereoselectivity of the reaction. (C) 2003 Elsevier Science Ltd. All rights reserved.

Enantiomerically pure phenanthroline or bipyridine containing macrocycles: a new class of ligands for asymmetric catalysis / A. Puglisi, M. Benaglia, R. Annunziata, A. Bologna. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 44:14(2003), pp. 2947-2951.

Enantiomerically pure phenanthroline or bipyridine containing macrocycles: a new class of ligands for asymmetric catalysis

A. Puglisi
Primo
;
M. Benaglia
Secondo
;
R. Annunziata
Penultimo
;
2003

Abstract

New enantiomerically pure plienanthroline- and bipyridine-containing macrocycles have been synthesized by combination of the coordinating unit to inexpensive and readily available chiral templates. The catalytic properties of their Cu(I) complexes have been Studied in the cyclopropanation of alkenes as test reaction. A simple structural modification of the chiral cavity allowed us to successfully control the trans or cis diastereoselectivity of the reaction. (C) 2003 Elsevier Science Ltd. All rights reserved.
English
Settore CHIM/06 - Chimica Organica
Articolo
Esperti anonimi
2003
44
14
2947
2951
Pubblicato
Periodico con rilevanza internazionale
info:eu-repo/semantics/article
Enantiomerically pure phenanthroline or bipyridine containing macrocycles: a new class of ligands for asymmetric catalysis / A. Puglisi, M. Benaglia, R. Annunziata, A. Bologna. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 44:14(2003), pp. 2947-2951.
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Prodotti della ricerca::01 - Articolo su periodico
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262
Article (author)
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A. Puglisi, M. Benaglia, R. Annunziata, A. Bologna
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/193726
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