8 article(s) from Kiss, Loránd
A study on selective transformation of norbornadiene into fluorinated cyclopentane-fused isoxazolines
- Zsanett Benke,
- Attila M. Remete and
- Loránd Kiss
Beilstein J. Org. Chem. 2021, 17, 2051–2066, doi:10.3762/bjoc.17.132
Synthesis of novel fluorinated building blocks via halofluorination and related reactions
- Attila Márió Remete,
- Tamás T. Novák,
- Melinda Nonn,
- Matti Haukka,
- Ferenc Fülöp and
- Loránd Kiss
Beilstein J. Org. Chem. 2020, 16, 2562–2575, doi:10.3762/bjoc.16.208
Ring-opening metathesis of some strained bicyclic systems; stereocontrolled access to diolefinated saturated heterocycles with multiple stereogenic centers
- Zsanett Benke,
- Melinda Nonn,
- Márton Kardos,
- Santos Fustero and
- Loránd Kiss
Beilstein J. Org. Chem. 2018, 14, 2698–2707, doi:10.3762/bjoc.14.247
Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence
- Attila Márió Remete,
- Melinda Nonn,
- Santos Fustero,
- Matti Haukka,
- Ferenc Fülöp and
- Loránd Kiss
Beilstein J. Org. Chem. 2017, 13, 2364–2371, doi:10.3762/bjoc.13.233
Novel stereocontrolled syntheses of tashiromine and epitashiromine
- Loránd Kiss,
- Enikő Forró and
- Ferenc Fülöp
Beilstein J. Org. Chem. 2015, 11, 596–603, doi:10.3762/bjoc.11.66
Efficient continuous-flow synthesis of novel 1,2,3-triazole-substituted β-aminocyclohexanecarboxylic acid derivatives with gram-scale production
- Sándor B. Ötvös,
- Ádám Georgiádes,
- István M. Mándity,
- Lóránd Kiss and
- Ferenc Fülöp
Beilstein J. Org. Chem. 2013, 9, 1508–1516, doi:10.3762/bjoc.9.172
Efficient regio- and stereoselective access to novel fluorinated β-aminocyclohexanecarboxylates
- Loránd Kiss,
- Melinda Nonn,
- Reijo Sillanpää,
- Santos Fustero and
- Ferenc Fülöp
Beilstein J. Org. Chem. 2013, 9, 1164–1169, doi:10.3762/bjoc.9.130
Synthesis of highly functionalized β-aminocyclopentanecarboxylate stereoisomers by reductive ring opening reaction of isoxazolines
- Melinda Nonn,
- Loránd Kiss,
- Reijo Sillanpää and
- Ferenc Fülöp
Beilstein J. Org. Chem. 2012, 8, 100–106, doi:10.3762/bjoc.8.10
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