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Organic Letters|May 5, 2006
1,2-Bisanionic coupling approach to 2,3-disubstituted cyclopentenols and cyclopentenonesMarco Luparia, Alessandro Vadalà, Giuseppe Zanoni, et al.
Organic Letters|April 26, 2013
Regio- and enantioselective cyclobutene allylationsSupaporn Niyomchon, Davide Audisio, Marco Luparia, et al.
Angewandte Chemie (International Ed. in English)|June 4, 2014
Asymmetric palladium-catalyzed allylic alkylation using dialkylzinc reagents: a remarkable ligand effectAntonio Misale, Supaporn Niyomchon, Marco Luparia, et al.
Organic Letters|September 10, 2015
From Stereodefined Cyclobutenes to Dienes: Total Syntheses of Ieodomycin D and the Southern Fragment of Macrolactin ACaroline Souris, Antonio Misale, Yong Chen, et al.
Chimia|July 2, 2014
Direct synthesis of stereodefined and functionalized dienes as valuable building blocksNuno Maulide, Caroline Souris, Frédéric Frébault, et al.
Natural Product Communications|May 13, 2011
Biomimetic cyclization of geraniol derivatives, a useful tool in the total synthesis of bioactive monocyclic terpenoidsValentina Merlini, Marco Luparia, Alessio Porta, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 14, 2009
A simple and versatile re-catalyzed Meyer-Schuster rearrangement of propargylic alcohols to alpha,beta-unsaturated carbonyl compoundsMassimo Stefanoni, Marco Luparia, Alessio Porta, et al.
Angewandte Chemie (International Ed. in English)|June 15, 2012
Diastereodivergent de-epimerization in catalytic asymmetric allylic alkylationDavide Audisio, Marco Luparia, Maria Teresa Oliveira, et al.
Chemistry & Biodiversity|July 12, 2008
Enantioselective synthesis and olfactory evaluation of 13-alkyl-substituted alpha-iononesMarco Luparia, Paolo Boschetti, Francesca Piccinini, et al.
The Journal of Organic Chemistry|September 12, 2009
Enantioselective synthesis and olfactory evaluation of bicyclic alpha- and gamma-ionone derivatives: the 3D arrangement of key molecular features relevant to the violet odor of iononesMarco Luparia, Laura Legnani, Alessio Porta, et al.
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