Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Fülöp

Showing results (1-10 of 48) with videos related to

Pageof 5
Sort By:
Farmaco (Societa Chimica Italiana : 1989)|August 5, 2000
Alicyclic beta-amino acids: useful synthons in drug researchF Fülöp
Current Medicinal Chemistry|October 16, 2012
Recent lipase-catalyzed hydrolytic approaches to pharmacologically important β- and γ-amino acidsE Forró, F Fülöp
Acta Pharmaceutica Hungarica|November 2, 1999
[Application of ring-chain tautomerism for the development of prodrugs]L Lázár, F Fülöp
Acta Pharmaceutica Hungarica|July 13, 1999
[Lipase-catalyzed resolution of 2-dialkylaminomethylcyclanols. Comparative studies]E Forró, F Fülöp
Journal of Chromatography. A|March 23, 2001
Liquid chromatographic enantioseparation of beta-blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agentM Péter, A Gyéresi, F Fülöp
Journal of Chromatography. A|March 29, 2000
Application of (1S,2S)- and (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propylisothiocyanate to the indirect enantioseparation of racemic proteinogenic amino acidsM Péter, A Péter, F Fülöp
Acta Pharmaceutica Hungarica|May 31, 2001
[High performance liquid chromatographic enantiomer separation of beta-blocking agents with a new isothiocyanate type chiral derivatizing agent]A Gyéresi, M Péter, F Fülöp
Bioorganic & Medicinal Chemistry Letters|December 23, 2017
Effects of newly synthetized isoquinoline derivatives on rat uterine contractility and ROCK II activityD Domokos, F Fülöp, G Falkay, et al.
Domestic Animal Endocrinology|October 30, 2016
Salsolinol-a potential inhibitor of the gonadotropic axis in sheep during lactationE Marciniak, M Hasiec, F Fülöp, et al.
Enantiomer|May 9, 2001
Study of diastereomeric thioureas formed with a new chiral derivatizing agentM Péter, A Perjéssy, D Loos, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Farmaco (Societa Chimica Italiana : 1989)|August 5, 2000
Alicyclic beta-amino acids: useful synthons in drug researchF Fülöp
Current Medicinal Chemistry|October 16, 2012
Recent lipase-catalyzed hydrolytic approaches to pharmacologically important β- and γ-amino acidsE Forró, F Fülöp
Acta Pharmaceutica Hungarica|November 2, 1999
[Application of ring-chain tautomerism for the development of prodrugs]L Lázár, F Fülöp
Acta Pharmaceutica Hungarica|July 13, 1999
[Lipase-catalyzed resolution of 2-dialkylaminomethylcyclanols. Comparative studies]E Forró, F Fülöp
Journal of Chromatography. A|March 23, 2001
Liquid chromatographic enantioseparation of beta-blocking agents with (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate as chiral derivatizing agentM Péter, A Gyéresi, F Fülöp
Journal of Chromatography. A|March 29, 2000
Application of (1S,2S)- and (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propylisothiocyanate to the indirect enantioseparation of racemic proteinogenic amino acidsM Péter, A Péter, F Fülöp
Acta Pharmaceutica Hungarica|May 31, 2001
[High performance liquid chromatographic enantiomer separation of beta-blocking agents with a new isothiocyanate type chiral derivatizing agent]A Gyéresi, M Péter, F Fülöp
Bioorganic & Medicinal Chemistry Letters|December 23, 2017
Effects of newly synthetized isoquinoline derivatives on rat uterine contractility and ROCK II activityD Domokos, F Fülöp, G Falkay, et al.
Domestic Animal Endocrinology|October 30, 2016
Salsolinol-a potential inhibitor of the gonadotropic axis in sheep during lactationE Marciniak, M Hasiec, F Fülöp, et al.
Enantiomer|May 9, 2001
Study of diastereomeric thioureas formed with a new chiral derivatizing agentM Péter, A Perjéssy, D Loos, et al.
Pageof 5