Search Results - "Donets, Pavel A."
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1
Ligand-Controlled Regiodivergent Nickel-Catalyzed Annulation of Pyridones
Published in Angewandte Chemie International Edition (07-01-2015)“…The 1,6‐annulated 2‐pyridone motif is found in many biologically active compounds and its close relation to the indolizidine and quinolizidine alkaloid core…”
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Journal Article -
2
Chiral Cp-Rhodium(III)-Catalyzed Asymmetric Hydroarylations of 1,1-Disubstituted Alkenes
Published in Angewandte Chemie International Edition (07-01-2014)“…Metal‐catalyzed functionalizations at the ortho position of a directing group have become an efficient bond‐forming strategy. A wide range of transformations…”
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Journal Article -
3
Diaminophosphine Oxide Ligand Enabled Asymmetric Nickel-Catalyzed Hydrocarbamoylations of Alkenes
Published in Journal of the American Chemical Society (14-08-2013)“…Chiral trivalent phosphorus species are the dominant class of ligands and the key controlling element in asymmetric homogeneous transition-metal catalysis…”
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4
Nickel(0)-Catalyzed Enantioselective Annulations of Alkynes and Arylenoates Enabled by a Chiral NHC Ligand: Efficient Access to Cyclopentenones
Published in Angewandte Chemie International Edition (24-11-2014)“…Cyclopentenones are versatile structural motifs of natural products as well as reactive synthetic intermediates. The nickel‐catalyzed reductive [3+2]…”
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5
Efficient Synthesis of the 3-Benzazepine Framework via Intramolecular Heck Reductive Cyclization
Published in Organic letters (02-08-2007)“…A microwave-assisted protocol based on reductive Heck reaction was developed for regio- and stereoselective construction of the 3-benzazepine core…”
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6
Efficient Synthesis of the Indoloazocine Framework via Intramolecular Alkyne Carbocyclization
Published in Organic letters (20-08-2009)“…A microwave-assisted protocol based on an Hg(OTf)2 catalyzed intramolecular alkyne carbocyclization reaction was developed for selective construction of the…”
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Journal Article -
7
Synthesis of the Azocino[cd]indole Framework through Pd-Catalyzed Intramolecular Acetylene Hydroarylation
Published in European Journal of Organic Chemistry (01-04-2011)“…The regio‐ and stereoselective construction of the azocino[cd]indole core was achieved by applying a Pd‐catalyzed intramolecular acetylene hydroarylation…”
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Book Review Journal Article -
8
Diversity-Oriented Microwave-Assisted Synthesis of the 3-Benzazepine Framework
Published in European Journal of Organic Chemistry (01-09-2010)“…An efficient diversity‐oriented procedure for the two‐step synthesis of 3‐benzazepines is described. The CuI‐catalyzed three‐component coupling of an aldehyde,…”
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9
Synthetic Approach toward Enantiopure Cyclic Sulfinamides
Published in Organic letters (01-07-2022)“…A synthetic approach toward densely substituted enantiopure cyclic sulfinamides possessing up to four consecutive stereogenic centers was developed based on a…”
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10
A 1,3,2‐Diazaphospholene‐Catalyzed Reductive Claisen Rearrangement
Published in Angewandte Chemie International Edition (24-06-2019)“…1,3,2‐Diazaphospholenes (DAPs) are an emerging class of organic hydrides. In this work, we exploited them as efficient catalysts for very mild reductive…”
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Journal Article -
11
Chiral 1,3,2‐Diazaphospholenes as Catalytic Molecular Hydrides for Enantioselective Conjugate Reductions
Published in Angewandte Chemie International Edition (03-04-2018)“…Secondary 1,3,2‐diazaphospholenes have a polarized P−H bond and are emerging as molecular hydrides. Herein, a class of chiral, conformationally restricted…”
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Journal Article -
12
Chiral Cp-Rhodium(III)-Catalyzed Asymmetric Hydroarylations of 1,1-Disubstituted Alkenes
Published in Angewandte Chemie (07-01-2014)“…Metal‐catalyzed functionalizations at the ortho position of a directing group have become an efficient bond‐forming strategy. A wide range of transformations…”
Get full text
Journal Article -
13
Nickel(0)-Catalyzed Enantioselective Annulations of Alkynes and Arylenoates Enabled by a Chiral NHC Ligand: Efficient Access to Cyclopentenones
Published in Angewandte Chemie (24-11-2014)“…Cyclopentenones are versatile structural motifs of natural products as well as reactive synthetic intermediates. The nickel‐catalyzed reductive [3+2]…”
Get full text
Journal Article -
14
A 1,3,2‐Diazaphospholene‐Catalyzed Reductive Claisen Rearrangement
Published in Angewandte Chemie (24-06-2019)“…1,3,2‐Diazaphospholenes (DAPs) are an emerging class of organic hydrides. In this work, we exploited them as efficient catalysts for very mild reductive…”
Get full text
Journal Article -
15
Ligand-Controlled Regiodivergent Nickel-Catalyzed Annulation of Pyridones
Published in Angewandte Chemie (07-01-2015)“…The 1,6‐annulated 2‐pyridone motif is found in many biologically active compounds and its close relation to the indolizidine and quinolizidine alkaloid core…”
Get full text
Journal Article -
16
Efficient Synthesis of the Indoloazocine Framework via Intramolecular Alkyne Carbocyclization
Published in Organic letters (20-04-2012)Get full text
Journal Article -
17
Chiral 1,3,2‐Diazaphospholenes as Catalytic Molecular Hydrides for Enantioselective Conjugate Reductions
Published in Angewandte Chemie (03-04-2018)“…Secondary 1,3,2‐diazaphospholenes have a polarized P−H bond and are emerging as molecular hydrides. Herein, a class of chiral, conformationally restricted…”
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Journal Article -
18
Chiral Monodentate Trialkylphosphines Based on the Phospholane Architecture
Published in Organometallics (10-12-2012)“…The development of efficient chiral monodentate phosphine ligands lags behind that of the bidentate congeners. This holds especially true for highly electron…”
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Journal Article -
19
Optimized Synthesis of Indole Carboxylate Metallo-β-Lactamase Inhibitor EBL-3183
Published in Organic process research & development (21-04-2023)“…A new synthetic route for the preparation of the metallo-β-lactamase inhibitor pre-candidate EBL-3183 was developed and carried out on a kilogram scale. The…”
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20
An Asymmetric Approach towards (–)‐Aphanorphine and Its Analogues
Published in European Journal of Organic Chemistry (01-02-2009)“…A short enantioselective approach towards the alkaloid(–)‐aphanorphine and its substituted analogues is described. The enantiomerically pure starting material…”
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