Patryk Niedbała

Has grant

Institute of Organic Chemistry, Polish Academy of Sciences

Poland

Research Interests

Explore related searches

Professors in Poland Professors in Organic Chemistry Organic Chemistry professors in Poland

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Recent Grants

Grant: Close

Kataliza Przeniesienia Fazowego w Trybie Przepływowym pod Wysokim Ciśnieniem

Open Date: 2019-01-21

Close Date: 2022-01-20

Grant: Close

Nowe katalizatory asymetrycznych reakcji przeniesienia fazowego - od prostych soli amoniowych do katalizy supramolekularnej

Open Date: 2017-01-18

Close Date: 2020-01-17

Grant: Close

Synteza nowych receptorów, ich zastosowanie w chiralnym rozopozniu biologicznie istotnych anionów oraz opracowanie dogodnych metod analizy tego zjawiska

Open Date: 2015-08-03

Close Date: 2018-08-02

Grant: Close

Nowe podejście do rozpoznania chiralnego organicznych kationów i anionów - dynamiczna chemia kombinatoryjna

Open Date: 2012-04-26

Close Date: 2016-11-26

Articles (10)

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Collaborators (1)

MAGDALENA CEBORSKA

Associate Professor

Cardinal Stefan Wyszyński University in Warsaw

POLAND

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Patryk Niedbała

Research Interests

Explore related searches

Contact this professor

Recent Grants

Articles (10)

H-Bond Mediated Phase-Transfer Catalysis: Enantioselective Generating of Quaternary Stereogenic Centers in β-Keto Esters

Anion Recognition by a Pincer-Type Host Constructed from Two Polyamide Macrocyclic Frameworks Jointed by a Photo-Addressable Azobenzene Switch

Recognition of Chiral Carboxylates by Synthetic Receptors

Assisted by Hydrogen-Bond Donors: Cinchona Quaternary Salts as Privileged Chiral Catalysts for Phase-Transfer Reactions

Solution and Solid State Studies of Urea Derivatives of DITIPIRAM Acting as Powerful Anion Receptors

A new class of “pincer” receptors – macrocyclic systems containing an incorporated amide group

Effective synthetic strategy towards highly selective macrocyclic anion receptors based on static combinatorial chemistry

Tuning Anion-Binding Properties of 22-Membered Unclosed Cryptands by Structural Modification of the Lariat Arm

One-Pot Parallel Synthesis of Unclosed Cryptands—Searching for Selective Anion Receptors via Static Combinatorial Chemistry Techniques

Synthesis of C2 Hybrid Amide‐Based PTC Catalysts and Their Comparison with Saturated Analogues

Collaborators (1)

MAGDALENA CEBORSKA

Make your next move.

Patryk Niedbała

Research Interests

Explore related searches

Contact this professor

Recent Grants

Articles (10)

H-Bond Mediated Phase-Transfer Catalysis: Enantioselective Generating of Quaternary Stereogenic Centers in &beta;-Keto Esters

Anion Recognition by a Pincer-Type Host Constructed from Two Polyamide Macrocyclic Frameworks Jointed by a Photo-Addressable Azobenzene Switch

Recognition of Chiral Carboxylates by Synthetic Receptors

Assisted by Hydrogen-Bond Donors: Cinchona Quaternary Salts as Privileged Chiral Catalysts for Phase-Transfer Reactions

Solution and Solid State Studies of Urea Derivatives of DITIPIRAM Acting as Powerful Anion Receptors

A new class of “pincer” receptors – macrocyclic systems containing an incorporated amide group

Effective synthetic strategy towards highly selective macrocyclic anion receptors based on static combinatorial chemistry

Tuning Anion-Binding Properties of 22-Membered Unclosed Cryptands by Structural Modification of the Lariat Arm

One-Pot Parallel Synthesis of Unclosed Cryptands—Searching for Selective Anion Receptors via Static Combinatorial Chemistry Techniques

Synthesis of C2 Hybrid Amide‐Based PTC Catalysts and Their Comparison with Saturated Analogues

Collaborators (1)

MAGDALENA CEBORSKA

Make your next move.

H-Bond Mediated Phase-Transfer Catalysis: Enantioselective Generating of Quaternary Stereogenic Centers in β-Keto Esters