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Selenium-directed conjugate addition of amines to 2-phenylseleno fumarate: regio- and diastereoselective synthesis of 2-phenylseleno-3-amino succinates 1997 Bella, Marco; Donofrio, F; Margarita, R; Parlanti, L; Piancatelli, Giovanni; Mangoni, A.
Direct amino-phenylselenylation of enoates: an easy route to alfa-phenylseleno-beta-amino esters and beta-lactams 1998 Torchiarolo, Gc; D'Onofrio, F; Margarita, R; Parlanti, L; Piancatelli, Giovanni; Bella, Marco
3-Phenylselanylfuran-2(5H)-one: a versatile building block in the synthesis of lignans. A new approach towards 3,4-dibenzyl g-butyrolactones. 1999 Piancatelli, Giovanni; Bella, Marco; Pigro, M. C.
“A Quantitative Measure of Borane Tert-Butylamine Complex Effectiveness in Carbonyl Reduction of Aged Papers.” 1999 Bicchieri, M.; Bella, Marco; Sementilli, F.
Asymmetric carbolithiation of 2-phenylselenofumarate derivatives: a short synthesis of (-)-roccellaric acid 2000 Bella, Marco; Margarita, R; Orlando, C; Orsini, M; Parlanti, L; Piancatelli, Giovanni
Direct vinylogous aldol addition of gamma-butyrolactones and gamma-butyrolactams 2000 Piancatelli, Giovanni; Bella, Marco; A., Squarcia; C., Trolli
PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, copper(I)-catalyzed allylic oxidation 2000 Malkov, Av; Bella, Marco; Langer, V; Kocovsky, P.
Efficient preparation of 3-substituted furan-2(5H)-ones and their direct vinylogous aldol addition. 2001 Bella, Marco; Piancatelli, Giovanni; Squarcia, A.
Modular pyridine-type P,N-ligands derived from monoterpenes: Application in asymmetric Heck addition 2001 Andrei V., Malkov; Bella, Marco; Irena G., Stara; Pavel, Kocovsky
Synthesis of new chiral 2,2 '-bipyridyl-type ligands, their coordination to molybdenum(0), copper(II), and palladium(II), and application in asymmetric allylic substitution, allylic oxidation, and cyclopropanation 2001 Malkov, Av; Baxendale, Ir; Bella, Marco; Langer, V; Fawcett, J; Russell, Dr; Mansfield, Dj; Valko, M; Kocovsky, P.
Construction of the complete aromatic core of diazonamide A by a novel hetero pinacol macrocyclization cascade reaction 2001 Nicolaou, Kc; Huang, X; Giuseppone, N; Rao, Pb; Bella, Marco; Reddy, Mv; Snyder, Sa
Total synthesis of diazonamide A 2002 K. C., Nicolaou; Bella, Marco; Dyk, Chen; Xianhai, Huang; Taotao, Ling; Scott A., Snyder
A novel regio- and stereoselective synthesis of sulfamidates from 1,2-diols using Burgess and related reagents: A facile entry into beta-amino alcohols 2002 Nicolaou, Kc; Huang, Xh; Snyder, Sa; Rao, Pb; Bella, Marco; Reddy, Mv
Synthesis of new chiral 2,2 '-bipyridine ligands and their application in copper-catalyzed asymmetric allylic oxidation and cyclopropanation 2003 Malkov, Av; Pernazza, D; Bell, M; Bella, Marco; Massa, A; Teply, F; Meghani, P; Kocovsky, P.
Synthetic studies on thiostrepton: Construction of thiostrepton analogues with the thiazoline-containing macrocycle 2003 K. C., Nicolaou; Marta, Nevalainen; Mark, Zak; Stephan, Bulat; Bella, Marco; Brian S., Safina
Organocatalytic asymmetric hydroxylation of beta-keto esters: Metal-free synthesis of optically active anti-diols 2004 Acocella, Mr; Mancheno, Og; Bella, Marco; Jorgensen, Ka
Chemistry of Odorants: Stereoselective Synthesis of Octahydronaphthalene-based perfumery Georgywood,(+,-)-1-[(1R*,2S*)-1,2,3,4,5,6,7,8-Octahydro-1,2,8,8-tetramethylnaphthalen-2-yl]ethan-1-one. 2004 Bella, Marco; Cianflone, M; Montemurro, G; Passacantilli, Pietro; Piancatelli, Giovanni
Studies toward diazonamide A: Development of a hetero-pinacol macrocyclization cascade for the construction of the bis-macrocyclic framework of the originally proposed structure 2004 Nicolaou, Kc; Snyder, Sa; Giuseppone, N; Huang, Xh; Bella, Marco; Reddy, Mv; Rao, Pb; Koumbis, Ae; Giannakakou, P; O'Brate, A.
Chemistry and biology of diazonamide A: First total synthesis and confirmation of the true structure 2004 Nicolaou, Kc; Chen, Dyk; Huang, Xh; Ling, Tt; Bella, Marco; Snyder, Sa
Organocatalytic enantioselective conjugate addition to alkynones 2004 Bella, Marco; Jorgensen, Ka
Mostrati risultati da 1 a 20 di 65
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