Summer Sale

Up to 30% off — ends 7 Aug

ONLY00h00m00s

Get 30% Off

Up to 30% off — ends 7 Aug

ONLY00h00m00s

Agnieszka Łapczuk

Cracow University of Technology

Poland

This profile is automatically generated from trusted academic sources.

Google Scholar

ORCID

How do I reach out?

Meet Kite AI

Contact this professor

ORCID

Google Scholar

Research Interests

Organic Chemistry

100%

Pharmaceutical Chemistry

50%

Cycloaddition Reactions

100%

Heterocyclic Chemistry

60%

Organic Reactions

50%

Macrocyclic Chemistry

40%

Chemical Synthesis

40%

Ask ApplyKite AI

Start chatting

How can you help me contact this professor?

What are this professor's research interests?

How should I write an email to this professor?

Articles14

The [3+2] cycloaddition reaction as an attractive way for the preparation of nicotine analogs (microreview)

Article Link

Year:

2023

Synthesis of (Z)-N-aryl-C-(pyrid-3-yl)-nitrones

Article Link

Year:

2023

Thermal [3+2] cycloaddition reactions as most universal way for the effective preparation of five-membered nitrogen containing heterocycles

Article Link

Year:

2023

On the Question of the Formation of Nitro-Functionalized 2,4-Pyrazole Analogs on the Basis of Nitrylimine Molecular Systems and 3,3,3-Trichloro-1-Nitroprop-1-Ene

Article Link

Year:

2022

On the Question of the Formation of Nitro-Functionalized 2,4-Pyrazole Analogs on the Basis of Nitrylimine Molecular Systems and 3,3,3-Trichloro-1-Nitroprop-1-Ene

Article Link

Year:

2022

On the Mechanism of the Synthesis of Nitrofunctionalised Δ2-Pyrazolines via [3+2] Cycloaddition Reactions between α-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

Article Link

Year:

2022

On the Mechanism of the Synthesis of Nitrofunctionalised Δ2-Pyrazolines via [3+2] Cycloaddition Reactions between α-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

Article Link

Year:

2022

A Comprehensive Experimental and Theoretical Study on the [{(η5-C5H5)2Zr[P(µ-PNEt2)2P(NEt2)2P]}]2O Crystalline System

Article Link

Year:

2021

Experimental and Theoretical Mechanistic Study on the Thermal Decomposition of 3,3-diphenyl-4-(trichloromethyl)-5-nitropyrazoline

Article Link

Year:

2021

Analysis of the possibility and molecular mechanism of carbon dioxide consumption in the Diels-Alder processes

Article Link

Year:

2021

A Comprehensive Experimental and Theoretical Study on the [{(eta(5)-C5H5)(2)Zr[P(mu-PNEt2)(2)P(NEt2)(2)P]}](2)O Crystalline System

Article Link

Year:

2021

Regio- and stereoselective synthesis of nitrofunctionalized 1,2-oxazolidine analogs of nicotine

Article Link

Year:

2020

Clean and molecularly programmable protocol for preparation of bis-heterobiarylic systems via a domino pseudocyclic reaction as a valuable alternative for TM-catalyzed cross-couplings

Article Link

Year:

2020

[3+2] Cycloaddition of diaryldiazomethanes with (E)-3,3,3-trichloro-1-nitroprop-1-ene: An experimental, theoretical and structural study

Article Link

Year:

2020

Collaborators4

Ewa Dresler

Łukasiewicz Research Network - Institute of Heavy Organic Synthesis "Blachownia"

POLAND

Karolina Kula

Professor's assistant

Cracow University of Technology

POLAND

Oleg M. Demchuk

John Paul II Catholic University of Lublin

POLAND

Radomir Jasiński

Cracow University of Technology

POLAND

How do I reach out?

Meet Kite AI

Agnieszka Łapczuk

How do I reach out?

Contact this professor

Research Interests

Ask ApplyKite AI

Articles14

The [3+2] cycloaddition reaction as an attractive way for the preparation of nicotine analogs (microreview)

Synthesis of (Z)-N-aryl-C-(pyrid-3-yl)-nitrones

Thermal [3+2] cycloaddition reactions as most universal way for the effective preparation of five-membered nitrogen containing heterocycles

On the Question of the Formation of Nitro-Functionalized 2,4-Pyrazole Analogs on the Basis of Nitrylimine Molecular Systems and 3,3,3-Trichloro-1-Nitroprop-1-Ene

On the Question of the Formation of Nitro-Functionalized 2,4-Pyrazole Analogs on the Basis of Nitrylimine Molecular Systems and 3,3,3-Trichloro-1-Nitroprop-1-Ene

On the Mechanism of the Synthesis of Nitrofunctionalised Δ<sup>2</sup>-Pyrazolines via [3+2] Cycloaddition Reactions between α-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

On the Mechanism of the Synthesis of Nitrofunctionalised Δ<SUP>2</SUP>-Pyrazolines via [3+2] Cycloaddition Reactions between α-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

A Comprehensive Experimental and Theoretical Study on the [{(η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>)<sub>2</sub>Zr[P(µ-PNEt<sub>2</sub>)<sub>2</sub>P(NEt<sub>2</sub>)<sub>2</sub>P]}]<sub>2</sub>O Crystalline System

Experimental and Theoretical Mechanistic Study on the Thermal Decomposition of 3,3-diphenyl-4-(trichloromethyl)-5-nitropyrazoline

Analysis of the possibility and molecular mechanism of carbon dioxide consumption in the Diels-Alder processes

A Comprehensive Experimental and Theoretical Study on the [{(eta(5)-C5H5)(2)Zr[P(mu-PNEt2)(2)P(NEt2)(2)P]}](2)O Crystalline System

Regio- and stereoselective synthesis of nitrofunctionalized 1,2-oxazolidine analogs of nicotine

Clean and molecularly programmable protocol for preparation of bis-heterobiarylic systems via a domino pseudocyclic reaction as a valuable alternative for TM-catalyzed cross-couplings

[3+2] Cycloaddition of diaryldiazomethanes with (E)-3,3,3-trichloro-1-nitroprop-1-ene: An experimental, theoretical and structural study

Collaborators4

Ewa Dresler

Karolina Kula

Oleg M. Demchuk

Radomir Jasiński

How do I reach out?

Agnieszka Łapczuk

How do I reach out?

Contact this professor

Research Interests

Ask ApplyKite AI

Articles14

The [3+2] cycloaddition reaction as an attractive way for the preparation of nicotine analogs (microreview)

Synthesis of (Z)-N-aryl-C-(pyrid-3-yl)-nitrones

Thermal [3+2] cycloaddition reactions as most universal way for the effective preparation of five-membered nitrogen containing heterocycles

On the Question of the Formation of Nitro-Functionalized 2,4-Pyrazole Analogs on the Basis of Nitrylimine Molecular Systems and 3,3,3-Trichloro-1-Nitroprop-1-Ene

On the Question of the Formation of Nitro-Functionalized 2,4-Pyrazole Analogs on the Basis of Nitrylimine Molecular Systems and 3,3,3-Trichloro-1-Nitroprop-1-Ene

On the Mechanism of the Synthesis of Nitrofunctionalised &Delta;<sup>2</sup>-Pyrazolines via [3+2] Cycloaddition Reactions between &alpha;-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

On the Mechanism of the Synthesis of Nitrofunctionalised Δ<SUP>2</SUP>-Pyrazolines via [3+2] Cycloaddition Reactions between α-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

A Comprehensive Experimental and Theoretical Study on the [{(&eta;<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>)<sub>2</sub>Zr[P(&micro;-PNEt<sub>2</sub>)<sub>2</sub>P(NEt<sub>2</sub>)<sub>2</sub>P]}]<sub>2</sub>O Crystalline System

Experimental and Theoretical Mechanistic Study on the Thermal Decomposition of 3,3-diphenyl-4-(trichloromethyl)-5-nitropyrazoline

Analysis of the possibility and molecular mechanism of carbon dioxide consumption in the Diels-Alder processes

A Comprehensive Experimental and Theoretical Study on the [{(eta(5)-C5H5)(2)Zr[P(mu-PNEt2)(2)P(NEt2)(2)P]}](2)O Crystalline System

Regio- and stereoselective synthesis of nitrofunctionalized 1,2-oxazolidine analogs of nicotine

Clean and molecularly programmable protocol for preparation of bis-heterobiarylic systems via a domino pseudocyclic reaction as a valuable alternative for TM-catalyzed cross-couplings

[3+2] Cycloaddition of diaryldiazomethanes with (E)-3,3,3-trichloro-1-nitroprop-1-ene: An experimental, theoretical and structural study

Collaborators4

Ewa Dresler

Karolina Kula

Oleg M. Demchuk

Radomir Jasiński

How do I reach out?

On the Mechanism of the Synthesis of Nitrofunctionalised Δ<sup>2</sup>-Pyrazolines via [3+2] Cycloaddition Reactions between α-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

A Comprehensive Experimental and Theoretical Study on the [{(η<sup>5</sup>-C<sub>5</sub>H<sub>5</sub>)<sub>2</sub>Zr[P(µ-PNEt<sub>2</sub>)<sub>2</sub>P(NEt<sub>2</sub>)<sub>2</sub>P]}]<sub>2</sub>O Crystalline System