Anna Gajda - Concepedia

Author

Anna Gajda

Lodz University of Technology ORCID

Also Known As

A GAJDA, A Gajda, Anna Gajda

Publications

252

Citations

H-Index

Concepts

All Affiliations

Lodz University of Technology Institute of Organic Chemistry Polish Academy of Sciences University of Łódź Ludwik Hirszfeld Institute of Immunology and Experimental Therapy

About

Anna Gajda is an author at Lodz University of Technology specializing in organic chemistry, chemistry, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	5	5	94
2	Engineering	4	4	86
3	Natural Sciences	4	4	82
4	Medicine	3	3	63
5	Biomolecular Engineering	2	2	28

Anna Gajda

Publications

195

Citations

H-Index

Page 1

	Year	Citations
A new access to substituted tetraethyl N-Boc 2-aminoethylidene-1,1-bisphosphonates and phosphonyl-substituted aza-Morita–Baylis–Hillman-type adducts Anna Gajda, Tadeusz Gajda Tetrahedron Tetraethyl N-boc 2-Aminoethylidene-1,1-bisphosphonatesInorganic ChemistryEngineeringOrganic ChemistryPhosphonyl-substituted Aza-morita–baylis–hillman-type Adducts	2007	35
Novel phosphonate analogs of sulforaphane: Synthesis, in vitro and in vivo anticancer activity Mateusz Psurski, Łukasz Janczewski, Marta Świtalska, European Journal of Medicinal Chemistry Medicinal ChemistryVivo Anticancer ActivityNovel Phosphonate AnalogsBiochemistryChemoprevention Strategy	2017	32
Direct, Microwave‐Assisted Synthesis of Isothiocyanates Łukasz Janczewski, Anna Gajda, Tadeusz Gajda European Journal of Organic Chemistry Chemical EngineeringEngineeringMicrowave‐assisted DesulfurationAvailable DithiocarbamatesMicrowave‐assisted Synthesis	2019	23
<i>N</i>-Carbamate Protected α-Amidoalkyl-<i>p</i>-tolylsulfones: Convenient Substrates in the aza-Morita−Baylis−Hillman Reaction Anna Gajda, Tadeusz Gajda The Journal of Organic Chemistry	2008	20
Synthesis and antiproliferative activity of novel α- and β-dialkoxyphosphoryl isothiocyanates Mateusz Psurski, K. M. Błażewska, Anna Gajda, Bioorganic & Medicinal Chemistry Letters Bioorganic Chemistryβ-Dialkoxyphosphoryl IsothiocyanatesBiochemistryMedicineNatural Sciences	2011	19
T3P® – A Benign Desulfurating Reagent in the Synthesis of Isothiocyanates Tadeusz Gajda, Łukasz Janczewski, Anna Gajda, Synthesis Chemical EngineeringDiversity Oriented SynthesisEngineeringBiochemistryNatural Sciences	2017	17
N-Carbamate α-aminoalkyl-p-tolylsulfones—convenient substrates in the nitro-Mannich synthesis of secondary N-carbamate protected syn-2-amino-1-nitroalkanephosphonates Roman Błaszczyk, Anna Gajda, Stefan Zawadzki, Tetrahedron BiochemistrySecondary N-carbamateN-carbamate α-Aminoalkyl-p-tolylsulfones—convenient SubstratesNitro-mannich SynthesisNatural Sciences	2010	14
Design, Synthesis, and Evaluation of ω‐(Isothiocyanato)alkylphosphinates and Phosphine Oxides as Antiproliferative Agents Łukasz Janczewski, Mateusz Psurski, Marta Świtalska, ChemMedChem	2017	12
The Anti-Tumoral Potential of Phosphonate Analog of Sulforaphane in Zebrafish Xenograft Model Magdalena Rudzińska, Łukasz Janczewski, Anna Gajda, Cells Diverse ItcsZebrafish Embryos 6Chemoprevention StrategyCellular PharmacologyZebrafish Xenograft Model	2021	12
Friedel–Crafts-type reaction of pyrene with diethyl 1-(isothiocyanato)alkylphosphonates. Efficient synthesis of highly fluorescent diethyl 1-(pyrene-1-carboxamido)alkylphosphonates and 1-(pyrene-1-carboxamido)methylphosphonic acid Anna Wrona‐Piotrowicz, Janusz Zakrzewski, Anna Gajda, Beilstein Journal of Organic Chemistry EngineeringMethylphosphonic AcidChemical DerivativeFluorous SynthesisOrganic Chemistry	2015	11

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