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ASYMMETRIC CATALYSIS
Synthesis of new chiral ligands
P-stereogenic compounds
Org. Lett. 2016, 18, 140-143
J. Org. Chem. 2019, 84, 4551-4557
Coordination chemistry
Chem. Commun. 2018, 54, 10132-10135
Transition-metal catalysis
Org. Lett. 2016, 18, 4040-4043
Org. Chem. Front. 2018, 5, 1600-1603
ChemCatChem 2017, 9, 728-732
SUPRAMOLECULAR CHEMISTRY
Design & synthesis of receptors
Cage molecules
Chem. Commun. 2019, 55, 14158-14161
Org. Lett. 2019, 21, 160-165
Phosphorus-based compounds
J. Am. Chem. Soc. 2017, 139, 6574-6577https://pubs.acs.org/doi/10.1021/jacs.7b02950
Eur. J. Org. Chem. 2016, 1619-1624https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201600080
Molecular recognition
Chem. Eur. J. 2019, 25, 3337-3342
Org. Lett. 2019, 21, 1999-2003
Org. Biomol. Chem. 2019, 17, 5253-5257
J. Org. Chem. 2020, 85, 4706-4711
Confined catalysis
Inorg. Chem. 2019, 58, 7220-7228
ACS Catal. 2017, 7, 7340-7345
ACS Catal. 2015, 5, 6748-6752
CHIRAL SEPARATION
Chiral HPLC at analytical and preparative scales
J. Org. Chem. 2015, 80, 4132-4141
Chirality 2019, 31, 481-491
J. Org. Chem. 2018, 83, 7566-7573
Org. Lett. 2019, 21, 3510-3513
Chiroptical properties
Chirality 2019, 31, 910-916https://onlinelibrary.wiley.com/doi/abs/10.1002/chir.23131
Chem. Sci. 2020, 11, 567-576
Dynamic stereochemistry/rotation barriers determinations
J. Org. Chem. 2017, 82, 10188-10200
J. Org. Chem. 2019, 84, 3169-3175
J. Org. Chem. 2015, 80, 1689-1695
