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Items: 7

1.

Regioselective O-Sulfonylation of N,N-Bis(2-hydroxyalkyl)tosylamides as a Synthetic Key Step to Enantiopure Morpholines.

Foschi F, Albanese D, Pecnikaj I, Tagliabue A, Penso M.

Org Lett. 2017 Jan 6;19(1):70-73. doi: 10.1021/acs.orglett.6b03342. Epub 2016 Dec 14.

PMID:
27966995
2.

Memory of chirality approach to the enantiodivergent synthesis of chiral benzo[d]sultams.

Foschi F, Tagliabue A, Mihali V, Pilati T, Pecnikaj I, Penso M.

Org Lett. 2013 Jul 19;15(14):3686-9. doi: 10.1021/ol401557v. Epub 2013 Jul 5.

PMID:
23829548
3.

Diastereoselective protocols for the synthesis of 2,3-trans- and 2,3-cis-6-methoxy-morpholine-2-carboxylic acid derivatives.

Penso M, Foschi F, Pellegrino S, Testa A, Gelmi ML.

J Org Chem. 2012 Apr 6;77(7):3454-61. doi: 10.1021/jo300221y. Epub 2012 Mar 21.

PMID:
22394367
4.

Enantioselective rearrangement of proline sulfonamides: an easy entry to enantiomerically pure α-aryl quaternary prolines.

Foschi F, Landini D, Lupi V, Mihali V, Penso M, Pilati T, Tagliabue A.

Chemistry. 2010 Sep 17;16(35):10667-70. doi: 10.1002/chem.201000989. No abstract available.

PMID:
20677198
5.

Highly stereoselective intramolecular alpha-arylation of self-stabilized non-racemic enolates: synthesis of alpha-quaternary alpha-amino acid derivatives.

Lupi V, Penso M, Foschi F, Gassa F, Mihali V, Tagliabue A.

Chem Commun (Camb). 2009 Sep 7;(33):5012-4. doi: 10.1039/b910326k. Epub 2009 Jul 13.

PMID:
19668833
6.

Complementary heterogeneous/homogeneous protocols for the synthesis of densely functionalized benzo[d]sultams: C-C bond formation by intramolecular nucleophilic aromatic fluorine displacement.

Penso M, Albanese D, Landini D, Lupi V, Tagliabue A.

J Org Chem. 2008 Sep 5;73(17):6686-90. doi: 10.1021/jo800930g. Epub 2008 Aug 8.

PMID:
18687000
7.

A New Synthesis of Functionalized 2-Alkylidenetetrahydro-5-furanones by Tandem Alkylation and Translactonization Reactions of 5(4H)-Oxazolones.

Cannella R, Clerici F, Gelmi ML, Penso M, Pocar D.

J Org Chem. 1996 Mar 8;61(5):1854-1856. No abstract available.

PMID:
11667061

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