![Sex Pheromone of the Alfalfa Plant Bug, Adelphocoris lineolatus: Pheromone Composition and Antagonistic Effect of 1-Hexanol (Hemiptera: Miridae) | SpringerLink Sex Pheromone of the Alfalfa Plant Bug, Adelphocoris lineolatus: Pheromone Composition and Antagonistic Effect of 1-Hexanol (Hemiptera: Miridae) | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10886-021-01273-y/MediaObjects/10886_2021_1273_Fig6_HTML.png)
Sex Pheromone of the Alfalfa Plant Bug, Adelphocoris lineolatus: Pheromone Composition and Antagonistic Effect of 1-Hexanol (Hemiptera: Miridae) | SpringerLink
![PDF) Synthetic- And DFT modelling studies on regioselective modified Mannich reactions of hydroxy-KYNA derivatives PDF) Synthetic- And DFT modelling studies on regioselective modified Mannich reactions of hydroxy-KYNA derivatives](https://i1.rgstatic.net/publication/348019589_Synthetic-_And_DFT_modelling_studies_on_regioselective_modified_Mannich_reactions_of_hydroxy-KYNA_derivatives/links/6382b91ec2cb154d292fd853/largepreview.png)
PDF) Synthetic- And DFT modelling studies on regioselective modified Mannich reactions of hydroxy-KYNA derivatives
Evaluation of the Antioxidant Activity of Cis/Trans-N-Phenyl-1,4,4a,5,8,8a-Hexahydro-3, 1-Benzoxazin-2-Imines
![IJMS | Free Full-Text | Synthesis of Indole-Coupled KYNA Derivatives via C–N Bond Cleavage of Mannich Bases IJMS | Free Full-Text | Synthesis of Indole-Coupled KYNA Derivatives via C–N Bond Cleavage of Mannich Bases](https://www.mdpi.com/ijms/ijms-23-07152/article_deploy/html/images/ijms-23-07152-sch001-550.jpg)
IJMS | Free Full-Text | Synthesis of Indole-Coupled KYNA Derivatives via C–N Bond Cleavage of Mannich Bases
![IJMS | Free Full-Text | Synthesis of Indole-Coupled KYNA Derivatives via C–N Bond Cleavage of Mannich Bases IJMS | Free Full-Text | Synthesis of Indole-Coupled KYNA Derivatives via C–N Bond Cleavage of Mannich Bases](https://www.mdpi.com/ijms/ijms-23-07152/article_deploy/html/images/ijms-23-07152-sch006.png)
IJMS | Free Full-Text | Synthesis of Indole-Coupled KYNA Derivatives via C–N Bond Cleavage of Mannich Bases
![Plants | Free Full-Text | Jacaranone Derivatives with Antiproliferative Activity from Crepis pulchra and Relevance of This Group of Plant Metabolites Plants | Free Full-Text | Jacaranone Derivatives with Antiproliferative Activity from Crepis pulchra and Relevance of This Group of Plant Metabolites](https://pub.mdpi-res.com/plants/plants-11-00782/article_deploy/html/images/plants-11-00782-g001.png?1647413717)
Plants | Free Full-Text | Jacaranone Derivatives with Antiproliferative Activity from Crepis pulchra and Relevance of This Group of Plant Metabolites
![Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/e1057f94-7305-45fe-b629-e84efcffeb49/tcr201700038-fig-0001-m.jpg)
Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library
![IJMS | Free Full-Text | Effective Activation by Kynurenic Acid and Its Aminoalkylated Derivatives on M-Type K+ Current IJMS | Free Full-Text | Effective Activation by Kynurenic Acid and Its Aminoalkylated Derivatives on M-Type K+ Current](https://www.mdpi.com/ijms/ijms-22-01300/article_deploy/html/images/ijms-22-01300-g003.png)
IJMS | Free Full-Text | Effective Activation by Kynurenic Acid and Its Aminoalkylated Derivatives on M-Type K+ Current
![Fluorine‐Containing Functionalized Cyclopentene Scaffolds Through Ring Contraction and Deoxofluorination of Various Substituted Cyclohexenes - Remete - 2018 - European Journal of Organic Chemistry - Wiley Online Library Fluorine‐Containing Functionalized Cyclopentene Scaffolds Through Ring Contraction and Deoxofluorination of Various Substituted Cyclohexenes - Remete - 2018 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/5784327c-c014-455a-bbd1-e3afea7ba65f/ejoc201800057-fig-0002-m.jpg)
Fluorine‐Containing Functionalized Cyclopentene Scaffolds Through Ring Contraction and Deoxofluorination of Various Substituted Cyclohexenes - Remete - 2018 - European Journal of Organic Chemistry - Wiley Online Library
![Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/868e9bd8-f791-4062-90e8-9ab2c9dd92f0/tcr201700038-fig-0003-m.jpg)
Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library
![Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/90656ed1-9756-4886-be79-5de8bd3ec872/tcr201700038-fig-0002-m.png)
Selective Synthesis of Fluorine‐Containing Cyclic β‐Amino Acid Scaffolds - Kiss - 2018 - The Chemical Record - Wiley Online Library
![Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4 ]triazolo[4,3- a ]pyrimidin-7(1 H )-ones - RSC Advances (RSC Publishing) DOI:10.1039/D0RA04345A Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4 ]triazolo[4,3- a ]pyrimidin-7(1 H )-ones - RSC Advances (RSC Publishing) DOI:10.1039/D0RA04345A](https://pubs.rsc.org/image/article/2020/RA/d0ra04345a/d0ra04345a-s1_hi-res.gif)
Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4 ]triazolo[4,3- a ]pyrimidin-7(1 H )-ones - RSC Advances (RSC Publishing) DOI:10.1039/D0RA04345A
![Molecules | Free Full-Text | Direct Enzymatic Route for the Preparation of Novel Enantiomerically Enriched Hydroxylated β-Amino Ester Stereoisomers Molecules | Free Full-Text | Direct Enzymatic Route for the Preparation of Novel Enantiomerically Enriched Hydroxylated β-Amino Ester Stereoisomers](https://pub.mdpi-res.com/molecules/molecules-15-03998/article_deploy/html/images/molecules-15-03998-ag.png?1541987595)
Molecules | Free Full-Text | Direct Enzymatic Route for the Preparation of Novel Enantiomerically Enriched Hydroxylated β-Amino Ester Stereoisomers
![Recent Progress in Aryltrifluoromethylation Reactions of Carbon‐Carbon Multiple Bonds - Remete - 2022 - Chemistry – An Asian Journal - Wiley Online Library Recent Progress in Aryltrifluoromethylation Reactions of Carbon‐Carbon Multiple Bonds - Remete - 2022 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/8dae9ba5-96ae-474b-9574-689871402ff9/asia202200395-fig-5004-m.jpg)
Recent Progress in Aryltrifluoromethylation Reactions of Carbon‐Carbon Multiple Bonds - Remete - 2022 - Chemistry – An Asian Journal - Wiley Online Library
![Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4 ]triazolo[4,3- a ]pyrimidin-7(1 H )-ones - RSC Advances (RSC Publishing) DOI:10.1039/D0RA04345A Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4 ]triazolo[4,3- a ]pyrimidin-7(1 H )-ones - RSC Advances (RSC Publishing) DOI:10.1039/D0RA04345A](https://pubs.rsc.org/image/article/2020/RA/d0ra04345a/d0ra04345a-s2_hi-res.gif)
Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4 ]triazolo[4,3- a ]pyrimidin-7(1 H )-ones - RSC Advances (RSC Publishing) DOI:10.1039/D0RA04345A
![PDF) Direct Enzymatic Route for the Preparation of Novel Enantiomerically Enriched Hydroxylated β-Amino Ester Stereoisomers PDF) Direct Enzymatic Route for the Preparation of Novel Enantiomerically Enriched Hydroxylated β-Amino Ester Stereoisomers](https://i1.rgstatic.net/publication/259452075_Direct_Enzymatic_Route_for_the_Preparation_of_Novel_Enantiomerically_Enriched_Hydroxylated_b-Amino_Ester_Stereoisomers/links/0912f509a17f4d6748000000/largepreview.png)