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Coinage Metal Complexes of the Carbenic Tautomer of a Conjugated Mesomeric Betaine Akin to Nitron

Molecules (Basel, Switzerland), 2017-07, Vol.22 (7), p.1133

2017

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Optimal dabigatran dosage in patients with moderate renal impairment

American journal of health-system pharmacy, 2013-12, Vol.70 (23), p.2067-2068

Leibold, Michael J

2013

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Carbonylation of the simplest persistent diaminocarbene

Chemical communications (Cambridge, England), 2013-01, Vol.49 (61), p.6834-6836

2013

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Ferrocene‐Based N ‐Heterocyclic Silylenes: Monomeric Silanechalcogenones, Silanimines, Silirenes, and Insertion Products with P 4

Chemistry : a European journal, 2024-06, Vol.30 (36)

2024

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When Does Carbonylation of Carbenes Yield Ketenes? A Theoretical Study with Implications for Synthesis

Journal of the American Chemical Society, 2011-03, Vol.133 (10), p.3557-3569

2011

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A crystalline cyclic (alkyl)(amino)carbene with a 1,1′-ferrocenylene backbone

Chemical communications (Cambridge, England), 2022-09, Vol.58 (74), p.1396-1399

2022

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Nitron: a stable N-heterocyclic carbene that has been commercially available for more than a century

Chemical communications (Cambridge, England), 2012-01, Vol.48 (2), p.227-229

2012

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Syntheses, Characterization and Reactivity of Iron(II), Nickel(II), Copper(II) and Zinc(II) Complexes of the Ligand N,N,N′,N′-Tetrakis(2-pyridylmethyl)benzene-1,3-diamine (1,3-tpbd) and Its Phenol Derivative 2,6-Bis[bis(2-pyridylmethyl)amino]-p-cresol (2,6-tpcd)

European Journal of Inorganic Chemistry, 2007-01, Vol.2007 (3), p.429-443

2007

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Redox‐Active N‐Heterocyclic Germylenes and Stannylenes with a Ferrocene‐1,1′‐diyl Backbone

Chemistry : a European journal, 2017-01, Vol.23 (5), p.1187-1199

2017

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A Stable Planar-Chiral N‑Heterocyclic Carbene with a 1,1′-Ferrocenediyl Backbone

Inorganic chemistry, 2015-07, Vol.54 (13), p.6657-6670

2015

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Ferrocene-Based N-Heterocyclic Plumbylenes [Fe{(η 5 -C 5 H 4 )NSiMe 2 R} 2 Pb:]: Influence of the Steric Demand of the N-Substituents on Their Dimerization via C-H Activation with Pb II

Chemistry, an Asian journal, 2023-07, Vol.18 (13), p.e202300266

2023

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New Stable and Persistent Acyclic Diaminocarbenes

Chemistry : a European journal, 2015-09, Vol.21 (40), p.14107-14121

2015

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Ferrocene‐Based N‐Heterocyclic Plumbylenes [Fe{(η5‐C5H4)NSiMe2R}2Pb:]: Influence of the Steric Demand of the N‐Substituents on Their Dimerization via C−H Activation with PbII

Chemistry, an Asian journal, 2023-07, Vol.18 (13), p.e202300266-n/a

2023

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Evaluation of benzthiazolidine-based formamidinium salts for the synthesis of penem-type β -lactams by uncatalysed carbonylation of acyclic diaminocarbenes

Zeitschrift für Naturforschung. B, A journal of chemical sciences, 2019-04, Vol.74 (4), p.365-372

2019

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N-heterocyclic carbenes which readily add ammonia, carbon monoxide and other small molecules

Chemical science (Cambridge), 2010-01, Vol.1 (6), p.697

2010

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Ferrocene-Based Bis(guanidines): Superbases for Tridentate N,Fe,N-Coordination

Organometallics, 2013-10, Vol.32 (20), p.5862-5872

2013

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Synthesis and Characterization of a Series of Nickel Complexes with Tripodal and Related Ligands: Electroreductive Coupling of Alkynes and Carbon Dioxide

European journal of inorganic chemistry, 2017-11, Vol.2017 (40), p.4722-4732

2017

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Six-Membered N-Heterocyclic Carbenes with a 1,1′-Ferrocenediyl Backbone: Bulky Ligands with Strong Electron-Donor Capacity and Unusual Non-Innocent Character

European Journal of Inorganic Chemistry, 2009-11, Vol.2009 (31), p.4607-4612

2009

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Nitron: a stable N-heterocyclic carbene that has been commercially available for more than a centuryPresented in part at the 19th EuCheMS International Conference on Organometallic Chemistry, Toulouse, July 2011.Electronic supplementary information (ESI) available: Experimental details including analytical and spectroscopic data, crystallographic and computational details, Fig. S1-S7, Tables S1-S3. CCDC 848861-848863. For ESI and crystallographic data in CIF or other electronic format see DOI: 1

2011-11

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Diastereoselective synthesis of a bicyclic β-lactam with penicillin G-like spectrum of activity by carbonylation of an acyclic diaminocarbene

Chemical communications (Cambridge, England), 2014-03, Vol.50 (18), p.2341-2343

2014

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Unexpected thermal decomposition of the "Alder carbene" (iPr2N)2C

Chemical communications (Cambridge, England), 2012-09, Vol.48 (73), p.9123-9125

2012

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Unexpected thermal decomposition of the "Alder carbene" (iPr2N)2CElectronic supplementary information (ESI) available: Experimental and computational details, Fig. S1-S5, Tables S1 and S2. See DOI: 10.1039/c2cc34208a

2012-08

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Unexpected thermal decomposition of the "Alder carbene" (iPr sub(2)N) sub(2)C

Chemical communications (Cambridge, England), 2012-08, Vol.48 (73), p.9123-9125

2012

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Carbonylation of the simplest persistent diaminocarbeneDedicated to Prof. Werner Uhl on the occasion of his 60th birthday.Electronic supplementary information (ESI) available: Experimental, crystallographic and computational details, Fig. S1S4. CCDC 916147 and 934512. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3cc42888e

2013-07

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Diastereoselective synthesis of a bicyclic β-lactam with penicillin G-like spectrum of activity by carbonylation of an acyclic diaminocarbeneElectronic supplementary information (ESI) available: Experimental, crystallographic and computational details, Fig. S1-S3 and Table S1. CCDC 951678. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c3cc48538b

2014-02

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Coinage Metal Complexes of the Carbenic Tautomer of a Conjugated Mesomeric Betaine Akin to Nitron

Optimal dabigatran dosage in patients with moderate renal impairment

Carbonylation of the simplest persistent diaminocarbene

Ferrocene‐Based N ‐Heterocyclic Silylenes: Monomeric Silanechalcogenones, Silanimines, Silirenes, and Insertion Products with P 4

When Does Carbonylation of Carbenes Yield Ketenes? A Theoretical Study with Implications for Synthesis

A crystalline cyclic (alkyl)(amino)carbene with a 1,1′-ferrocenylene backbone

Nitron: a stable N-heterocyclic carbene that has been commercially available for more than a century

Syntheses, Characterization and Reactivity of Iron(II), Nickel(II), Copper(II) and Zinc(II) Complexes of the Ligand N,N,N′,N′-Tetrakis(2-pyridylmethyl)benzene-1,3-diamine (1,3-tpbd) and Its Phenol Derivative 2,6-Bis[bis(2-pyridylmethyl)amino]-p-cresol (2,6-tpcd)

Redox‐Active N‐Heterocyclic Germylenes and Stannylenes with a Ferrocene‐1,1′‐diyl Backbone

A Stable Planar-Chiral N‑Heterocyclic Carbene with a 1,1′-Ferrocenediyl Backbone

Ferrocene-Based N-Heterocyclic Plumbylenes [Fe{(η 5 -C 5 H 4 )NSiMe 2 R} 2 Pb:]: Influence of the Steric Demand of the N-Substituents on Their Dimerization via C-H Activation with Pb II

New Stable and Persistent Acyclic Diaminocarbenes

Ferrocene‐Based N‐Heterocyclic Plumbylenes [Fe{(η5‐C5H4)NSiMe2R}2Pb:]: Influence of the Steric Demand of the N‐Substituents on Their Dimerization via C−H Activation with PbII

Evaluation of benzthiazolidine-based formamidinium salts for the synthesis of penem-type β -lactams by uncatalysed carbonylation of acyclic diaminocarbenes

N-heterocyclic carbenes which readily add ammonia, carbon monoxide and other small molecules

Ferrocene-Based Bis(guanidines): Superbases for Tridentate N,Fe,N-Coordination

Synthesis and Characterization of a Series of Nickel Complexes with Tripodal and Related Ligands: Electroreductive Coupling of Alkynes and Carbon Dioxide

Six-Membered N-Heterocyclic Carbenes with a 1,1′-Ferrocenediyl Backbone: Bulky Ligands with Strong Electron-Donor Capacity and Unusual Non-Innocent Character

Diastereoselective synthesis of a bicyclic β-lactam with penicillin G-like spectrum of activity by carbonylation of an acyclic diaminocarbene

Unexpected thermal decomposition of the "Alder carbene" (iPr2N)2C

Unexpected thermal decomposition of the "Alder carbene" (iPr2N)2CElectronic supplementary information (ESI) available: Experimental and computational details, Fig. S1-S5, Tables S1 and S2. See DOI: 10.1039/c2cc34208a

Unexpected thermal decomposition of the "Alder carbene" (iPr sub(2)N) sub(2)C

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