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Chiral Organosulfur Ligands/Catalysts with a Stereogenic Sulfur Atom: Applications in Asymmetric Synthesis

Chemical reviews, 2017-03, Vol.117 (5), p.4147-4181

2017

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Highly Z -Selective Horner-Wadsworth-Emmons Olefination Using Modified Still-Gennari-Type Reagents

Molecules (Basel, Switzerland), 2022-10, Vol.27 (20), p.7138

2022

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Still–Gennari Olefination and its Applications in Organic Synthesis

Advanced synthesis & catalysis, 2020-07, Vol.362 (13), p.2552-2596

2020

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The Comparison of MTT and CVS Assays for the Assessment of Anticancer Agent Interactions

PloS one, 2016-05, Vol.11 (5), p.e0155772-e0155772

2016

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A Straightforward, Purification-Free Procedure for the Synthesis of Ando and Still–Gennari Type Phosphonates

Synthesis (Stuttgart), 2022-01, Vol.54 (2), p.378-382

2022

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Towards Chemoenzymatic Syntheses of Both Enantiomers of Phosphoemeriamine

Molecules (Basel, Switzerland), 2024-04, Vol.29 (8), p.1799

2024

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Enzymatic Approach to the Synthesis of Enantiomerically Pure Hydroxy Derivatives of 1,3,5-Triaza-7-phosphaadamantane

Journal of organic chemistry, 2021-07, Vol.86 (13), p.8556-8562

2021

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Application of the Z-Selective Still–Gennari Olefination Protocol for the Synthesis of Z-α,β-Unsaturated Phosphonates

Synthesis (Stuttgart), 2018-10, Vol.50 (20), p.4140-4144

2018

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New Optically Active tert -Butylarylthiophosphinic Acids and Their Selenium Analogues as the Potential Synthons of Supramolecular Organometallic Complexes: Syntheses and Crystallographic Structure Determination

Molecules (Basel, Switzerland), 2023-05, Vol.28 (11), p.4298

2023

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Chiral Hypervalent, Pentacoordinated Phosphoranes

Molecules, 2016-11, Vol.21 (11), p.1573

2016

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An Organofluorine Isoselenocyanate Analogue of Sulforaphane Affects Antimetabolite 5-Fluorouracil's Anticancer Activity: A Perspective for New Combinatory Therapy in Triple-Negative Breast Cancer

Molecules (Basel, Switzerland), 2023-08, Vol.28 (15), p.5808

2023

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Attempts at the enzymatic synthesis of chiral ester derivatives of 1,3,5-triaza-7-phosphaadamantane (PTA)

Phosphorus, sulfur, and silicon and the related elements, 2022-06, Vol.197 (5-6), p.639-643

2022

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The first enzyme-promoted addition of nitromethane to imines (aza-Henry reaction)

Bioorganic chemistry, 2020-01, Vol.94, p.103377-103377, Article 103377

2020

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Quarter of a Century after: A Glimpse at the Conformation and Mechanism of Candida antarctica Lipase B

Crystals (Basel), 2020-05, Vol.10 (5), p.404

2020

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Asymmetric Bioreduction of β‐Activated Vinylphosphonate Derivatives Using Ene‐Reductases

Advanced synthesis & catalysis, 2017-12, Vol.359 (23), p.4190-4196

2017

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Enzymatic Desymmetrisation of Prochiral Phosphines and Phosphine P-Sulfides as a Route to P-Chiral Catalysts

Catalysts, 2022-02, Vol.12 (2), p.171

2022

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Enzymatic kinetic resolution in the synthesis of new precursors of P- chiral organophosphorus catalysts: phosphines and their P- boranes

Phosphorus, sulfur, and silicon and the related elements, 2022-06, Vol.197 (5-6), p.564-567

2022

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Afterword: Twenty third international conference on phosphorus chemistry

Phosphorus, sulfur, and silicon and the related elements, 2022-06, Vol.197 (5-6), p.661-661

2022

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Biocatalysis in Organosulfur Chemistry

Phosphorus, sulfur, and silicon and the related elements, 2011-05, Vol.186 (5), p.1104-1118

Kielbasinski, Piotr

2011

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Enzyme-promoted kinetic resolution of acetoxymethyl aryl sulfoxides

Journal of molecular catalysis. B, Enzymatic, 2015-08, Vol.118, p.23-28

2015

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Sulforaphane derivatives containing triazaphosphaadamantane (PTA) or o -carborane substituent

Phosphorus, sulfur, and silicon and the related elements, 2022-06, Vol.197 (5-6), p.554-556

2022

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Highly Efficient Asymmetric Simmons-Smith Cyclopropanation Promoted by Chiral Heteroorganic Aziridinyl Ligands

ChemCatChem, 2014-03, Vol.6 (3), p.873-875

2014

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Preparative scale application of Mucor circinelloides ene–reductase and alcohol dehydrogenase activity for the asymmetric bioreduction of α,β-unsaturated γ-ketophosphonates

Bioorganic chemistry, 2020-03, Vol.96, p.103548, Article 103548

2020

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Fluoroaryl analogs of sulforaphane – A group of compounds of anticancer and antimicrobial activity

Bioorganic chemistry, 2020-01, Vol.94, p.103454, Article 103454

2020

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Lipase-mediated stereoselective transformations of chiral organophosphorus P-boranes revisited: revision of the absolute configuration of alkoxy(hydroxymethyl)phenylphosphine P-boranes

Tetrahedron: asymmetry, 2011-07, Vol.22 (14), p.1581-1590

2011

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Chiral Organosulfur Ligands/Catalysts with a Stereogenic Sulfur Atom: Applications in Asymmetric Synthesis

Highly Z -Selective Horner-Wadsworth-Emmons Olefination Using Modified Still-Gennari-Type Reagents

Still–Gennari Olefination and its Applications in Organic Synthesis

The Comparison of MTT and CVS Assays for the Assessment of Anticancer Agent Interactions

A Straightforward, Purification-Free Procedure for the Synthesis of Ando and Still–Gennari Type Phosphonates

Towards Chemoenzymatic Syntheses of Both Enantiomers of Phosphoemeriamine

Enzymatic Approach to the Synthesis of Enantiomerically Pure Hydroxy Derivatives of 1,3,5-Triaza-7-phosphaadamantane

Application of the Z-Selective Still–Gennari Olefination Protocol for the Synthesis of Z-α,β-Unsaturated Phosphonates

New Optically Active tert -Butylarylthiophosphinic Acids and Their Selenium Analogues as the Potential Synthons of Supramolecular Organometallic Complexes: Syntheses and Crystallographic Structure Determination

Chiral Hypervalent, Pentacoordinated Phosphoranes

An Organofluorine Isoselenocyanate Analogue of Sulforaphane Affects Antimetabolite 5-Fluorouracil's Anticancer Activity: A Perspective for New Combinatory Therapy in Triple-Negative Breast Cancer

Attempts at the enzymatic synthesis of chiral ester derivatives of 1,3,5-triaza-7-phosphaadamantane (PTA)

The first enzyme-promoted addition of nitromethane to imines (aza-Henry reaction)

Quarter of a Century after: A Glimpse at the Conformation and Mechanism of Candida antarctica Lipase B

Asymmetric Bioreduction of β‐Activated Vinylphosphonate Derivatives Using Ene‐Reductases

Enzymatic Desymmetrisation of Prochiral Phosphines and Phosphine P-Sulfides as a Route to P-Chiral Catalysts

Enzymatic kinetic resolution in the synthesis of new precursors of P- chiral organophosphorus catalysts: phosphines and their P- boranes

Afterword: Twenty third international conference on phosphorus chemistry

Biocatalysis in Organosulfur Chemistry

Enzyme-promoted kinetic resolution of acetoxymethyl aryl sulfoxides

Sulforaphane derivatives containing triazaphosphaadamantane (PTA) or o -carborane substituent

Highly Efficient Asymmetric Simmons-Smith Cyclopropanation Promoted by Chiral Heteroorganic Aziridinyl Ligands

Preparative scale application of Mucor circinelloides ene–reductase and alcohol dehydrogenase activity for the asymmetric bioreduction of α,β-unsaturated γ-ketophosphonates

Fluoroaryl analogs of sulforaphane – A group of compounds of anticancer and antimicrobial activity

Lipase-mediated stereoselective transformations of chiral organophosphorus P-boranes revisited: revision of the absolute configuration of alkoxy(hydroxymethyl)phenylphosphine P-boranes

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