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Items: 14

1.

Carboxamido steroids inhibit the opening properties of transient receptor potential ion channels by lipid raft modulation.

Sághy É, Payrits M, Bíró-Sütő T, Skoda-Földes R, Szánti-Pintér E, Erostyák J, Makkai G, Sétáló G Jr, Kollár L, Kőszegi T, Csepregi R, Szolcsányi J, Helyes Z, Szőke É.

J Lipid Res. 2018 Oct;59(10):1851-1863. doi: 10.1194/jlr.M084723. Epub 2018 Aug 9.

2.

Synthesis of 16α-amino-pregnenolone derivatives via ionic liquid-catalyzed aza-Michael addition and their evaluation as C17,20-lyase inhibitors.

Szánti-Pintér E, Maksó L, Gömöry Á, Wouters J, Edina Herman B, Szécsi M, Mikle G, Kollár L, Skoda-Földes R.

Steroids. 2017 Jul;123:61-66. doi: 10.1016/j.steroids.2017.05.006. Epub 2017 May 11.

PMID:
28502863
3.

Synthesis of novel 13α-18-norandrostane-ferrocene conjugates via homogeneous catalytic methods and their investigation on TRPV1 receptor activation.

Szánti-Pintér E, Wouters J, Gömöry Á, Sághy É, Szőke É, Helyes Z, Kollár L, Skoda-Földes R.

Steroids. 2015 Dec;104:284-93. doi: 10.1016/j.steroids.2015.10.016. Epub 2015 Oct 28.

PMID:
26519768
4.

The use of supported acidic ionic liquids in organic synthesis.

Skoda-Földes R.

Molecules. 2014 Jun 26;19(7):8840-84. doi: 10.3390/molecules19078840. Review.

5.

Synthesis of novel 13α-18-nor-16-carboxamido steroids via a palladium-catalyzed aminocarbonylation reaction.

Szánti-Pintér E, Csók Z, Berente Z, Kollár L, Skoda-Földes R.

Steroids. 2013 Dec 11;78(12-13):1177-82. doi: 10.1016/j.steroids.2013.08.011. Epub 2013 Sep 5.

PMID:
24012726
6.

Synthesis of ferrocene-labeled steroids via copper-catalyzed azide-alkyne cycloaddition. Reactivity difference between 2β-, 6β- and 16β-azido-androstanes.

Fehér K, Balogh J, Csók Z, Kégl T, Kollár L, Skoda-Földes R.

Steroids. 2012 Jun;77(7):738-44. doi: 10.1016/j.steroids.2012.04.005. Epub 2012 Apr 13.

PMID:
22521424
7.

Synthesis of steroid-ferrocene conjugates of steroidal 17-carboxamides via a palladium-catalyzed aminocarbonylation--copper-catalyzed azide-alkyne cycloaddition reaction sequence.

Szánti-Pintér E, Balogh J, Csók Z, Kollár L, Gömöry A, Skoda-Földes R.

Steroids. 2011 Nov;76(12):1377-82. doi: 10.1016/j.steroids.2011.07.006. Epub 2011 Jul 20.

PMID:
21787798
8.

Ionic liquid-promoted Wagner-Meerwein rearrangement of 16α,17α-epoxyandrostanes and 16α,17α-epoxyestranes.

Horváth A, Szájli Á, Kiss R, Kóti J, Mahó S, Skoda-Földes R.

J Org Chem. 2011 Aug 5;76(15):6048-56. doi: 10.1021/jo2006285. Epub 2011 Jul 5.

PMID:
21668005
9.

Facile ring opening of 2,3-epoxy-steroids with aromatic amines in ionic liquids.

Horváth A, Skoda-Földes R, Mahó S, Berente Z, Kollár L.

Steroids. 2006 Aug;71(8):706-11. Epub 2006 Jun 5.

PMID:
16750547
10.

Unexpected reactivity difference between iodo-alkene moieties of steroids possessing remote lactame or cycloalkane structural units: a theoretical approach.

Kunsági-Máté S, Skoda-Földes R, Szepes L, Végh E, Kollár L.

J Biochem Biophys Methods. 2004 Oct 29;61(1-2):69-75.

PMID:
15560923
11.

Transition-metal-catalyzed reactions in steroid synthesis.

Skoda-Földes R, Kollár L.

Chem Rev. 2003 Oct;103(10):4095-130. Review. No abstract available.

PMID:
14531719
12.

Microwave-assisted Stille-coupling of steroidal substrates.

Skoda-Földes R, Pfeiffer P, Horváth J, Tuba Z, Kollár L.

Steroids. 2002 Jul;67(8):709-13.

PMID:
12117618
13.

Synthesis of steroidal diacyl hydrazines and their 1,3,4-oxadiazole derivatives.

Szarka Z, Skoda-Földes R, Horváth J, Tuba Z, Kollár L.

Steroids. 2002 Jun;67(7):581-6.

PMID:
11996930
14.

Synthesis of N-Substituted Steroidal Hydrazides in Homogeneous Catalytic Hydrazinocarbonylation Reaction.

Skoda-Földes R, Szarka Z, Kollár L, Dinya Z, Horváth J, Tuba Z.

J Org Chem. 1999 Mar 19;64(6):2134-2136. No abstract available.

PMID:
11674314

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