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1
Rh(III) -Catalyzed C-H Activation with Pyridotriazoles: Direct Access to Fluorophores for Metal-Ion Detection
Rh(III) -Catalyzed C-H Activation with Pyridotriazoles: Direct Access to Fluorophores for Metal-Ion Detection
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Rh(III) -Catalyzed C-H Activation with Pyridotriazoles: Direct Access to Fluorophores for Metal-Ion Detection

Angewandte Chemie (International ed.), 2015-09, Vol.54 (37), p.10975-10979 [Peer Reviewed Journal]

2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201504757 ;PMID: 26211642

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2
Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products
Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products
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Rhodium-Catalyzed Ketone Methylation Using Methanol Under Mild Conditions: Formation of α-Branched Products

Angewandte Chemie (International ed.), 2014-01, Vol.53 (3), p.761-765 [Peer Reviewed Journal]

2014 The Authors. Published by Wiley‐VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. ;2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. ;2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. 2014 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201307950 ;PMID: 24288297

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3
The C-H activation/1,3-diyne strategy: highly selective direct synthesis of diverse bisheterocycles by Rh(III) catalysis
The C-H activation/1,3-diyne strategy: highly selective direct synthesis of diverse bisheterocycles by Rh(III) catalysis
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The C-H activation/1,3-diyne strategy: highly selective direct synthesis of diverse bisheterocycles by Rh(III) catalysis

Angewandte Chemie (International ed.), 2014-09, Vol.53 (36), p.9650-9654 [Peer Reviewed Journal]

2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201403782 ;PMID: 24986535

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4
An Efficient Low-Temperature Route to Polycyclic Isoquinoline Salt Synthesis via C−H Activation with [CpMCl2]2 (M = Rh, Ir)
An Efficient Low-Temperature Route to Polycyclic Isoquinoline Salt Synthesis via C−H Activation with [CpMCl2]2 (M = Rh, Ir)
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An Efficient Low-Temperature Route to Polycyclic Isoquinoline Salt Synthesis via C−H Activation with [CpMCl2]2 (M = Rh, Ir)

Journal of the American Chemical Society, 2008-09, Vol.130 (37), p.12414-12419 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja802415h ;PMID: 18714995

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5
Versatile Reactivity of Rhodium-Iminocarbenes Derived from N-Sulfonyl Triazoles
Versatile Reactivity of Rhodium-Iminocarbenes Derived from N-Sulfonyl Triazoles
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Versatile Reactivity of Rhodium-Iminocarbenes Derived from N-Sulfonyl Triazoles

Angewandte Chemie (International ed.), 2013-01, Vol.52 (5), p.1371-1373 [Peer Reviewed Journal]

Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2013 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim 2013 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201209338 ;PMID: 23297004 ;CODEN: ACIEAY

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6
Catalytic activation of carbon-carbon bonds in cyclopentanones
Catalytic activation of carbon-carbon bonds in cyclopentanones
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Catalytic activation of carbon-carbon bonds in cyclopentanones

Nature (London), 2016-11, Vol.539 (7630), p.546-550 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 24, 2016 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature19849 ;PMID: 27806379 ;CODEN: NATUAS

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7
Site-selective and stereoselective functionalization of non-activated tertiary C-H bonds
Site-selective and stereoselective functionalization of non-activated tertiary C-H bonds
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Site-selective and stereoselective functionalization of non-activated tertiary C-H bonds

Nature (London), 2017-11, Vol.551 (7682), p.609-613 [Peer Reviewed Journal]

Copyright Nature Publishing Group Nov 30, 2017 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature24641 ;PMID: 29156454

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8
Rhodium-Catalyzed Transannulation of 1,2,3-Triazoles with Nitriles
Rhodium-Catalyzed Transannulation of 1,2,3-Triazoles with Nitriles
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Rhodium-Catalyzed Transannulation of 1,2,3-Triazoles with Nitriles

Journal of the American Chemical Society, 2008-11, Vol.130 (45), p.14972-14974 [Peer Reviewed Journal]

Copyright © 2008 American Chemical Society ;ISSN: 0002-7863 ;EISSN: 1520-5126 ;DOI: 10.1021/ja805079v ;PMID: 18855475

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9
Cooperative activation of cyclobutanones and olefins leads to bridged ring systems by a catalytic [4 + 2] coupling
Cooperative activation of cyclobutanones and olefins leads to bridged ring systems by a catalytic [4 + 2] coupling
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Cooperative activation of cyclobutanones and olefins leads to bridged ring systems by a catalytic [4 + 2] coupling

Nature chemistry, 2014-08, Vol.6 (8), p.739-744 [Peer Reviewed Journal]

Copyright Nature Publishing Group Aug 2014 ;ISSN: 1755-4330 ;EISSN: 1755-4349 ;DOI: 10.1038/nchem.1989 ;PMID: 25054946

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10
Engineering a dirhodium artificial metalloenzyme for selective olefin cyclopropanation
Engineering a dirhodium artificial metalloenzyme for selective olefin cyclopropanation
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Engineering a dirhodium artificial metalloenzyme for selective olefin cyclopropanation

Nature communications, 2015-07, Vol.6 (1), p.7789, Article 7789 [Peer Reviewed Journal]

Copyright Nature Publishing Group Jul 2015 ;Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2015 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/ncomms8789 ;PMID: 26206238

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11
Rhodium(III)-Catalyzed Amidation of Unactivated C(sp3)H Bonds
Rhodium(III)-Catalyzed Amidation of Unactivated C(sp3)H Bonds
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Rhodium(III)-Catalyzed Amidation of Unactivated C(sp3)H Bonds

Angewandte Chemie (International ed.), 2015-10, Vol.54 (44), p.13049-13052 [Peer Reviewed Journal]

2015 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright Wiley Subscription Services, Inc. Oct 2015 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201506323 ;PMID: 26480337 ;CODEN: ACIEAY

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12
Domino reactions of rhodium(II) carbenoids for alkaloid synthesis
Domino reactions of rhodium(II) carbenoids for alkaloid synthesis
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Domino reactions of rhodium(II) carbenoids for alkaloid synthesis

Chemical Society reviews, 2009-01, Vol.38 (11), p.3072-3081 [Peer Reviewed Journal]

ISSN: 0306-0012 ;EISSN: 1460-4744 ;DOI: 10.1039/b816701j ;PMID: 19847342

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13
Metallo-intercalators and metallo-insertors
Metallo-intercalators and metallo-insertors
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Metallo-intercalators and metallo-insertors

Chemical communications (Cambridge, England), 2007-01 (44), p.4565-4579 [Peer Reviewed Journal]

ISSN: 1359-7345 ;EISSN: 1364-548X ;DOI: 10.1039/b710949k ;PMID: 17989802

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14
Rhodium-catalysed syn-carboamination of alkenes via a transient directing group
Rhodium-catalysed syn-carboamination of alkenes via a transient directing group
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Rhodium-catalysed syn-carboamination of alkenes via a transient directing group

Nature (London), 2015-11, Vol.527 (7576), p.86-90 [Peer Reviewed Journal]

COPYRIGHT 2015 Nature Publishing Group ;COPYRIGHT 2015 Nature Publishing Group ;Copyright Nature Publishing Group Nov 5, 2015 ;ISSN: 0028-0836 ;EISSN: 1476-4687 ;DOI: 10.1038/nature15691 ;PMID: 26503048 ;CODEN: NATUAS

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15
Construction of Axial Chirality by Rhodium-Catalyzed Asymmetric Dehydrogenative Heck Coupling of Biaryl Compounds with Alkenes
Construction of Axial Chirality by Rhodium-Catalyzed Asymmetric Dehydrogenative Heck Coupling of Biaryl Compounds with Alkenes
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Construction of Axial Chirality by Rhodium-Catalyzed Asymmetric Dehydrogenative Heck Coupling of Biaryl Compounds with Alkenes

Angewandte Chemie (International ed.), 2014-11, Vol.53 (48), p.13244-13247 [Peer Reviewed Journal]

2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201408805 ;PMID: 25346171 ;CODEN: ACIEAY

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16
Synthesis of Pd-Rh Core-Frame Concave Nanocubes and Their Conversion to Rh Cubic Nanoframes by Selective Etching of the Pd Cores
Synthesis of Pd-Rh Core-Frame Concave Nanocubes and Their Conversion to Rh Cubic Nanoframes by Selective Etching of the Pd Cores
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Synthesis of Pd-Rh Core-Frame Concave Nanocubes and Their Conversion to Rh Cubic Nanoframes by Selective Etching of the Pd Cores

Angewandte Chemie (International ed.), 2012-10, Vol.51 (41), p.10266-10270 [Peer Reviewed Journal]

Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201206044 ;PMID: 22968993 ;CODEN: ACIEAY

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17
Rhodium(II)-Catalyzed Intramolecular Annulation of 1-Sulfonyl-1,2,3-Triazoles with Pyrrole and Indole Rings: Facile Synthesis of N-Bridgehead Azepine Skeletons
Rhodium(II)-Catalyzed Intramolecular Annulation of 1-Sulfonyl-1,2,3-Triazoles with Pyrrole and Indole Rings: Facile Synthesis of N-Bridgehead Azepine Skeletons
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Rhodium(II)-Catalyzed Intramolecular Annulation of 1-Sulfonyl-1,2,3-Triazoles with Pyrrole and Indole Rings: Facile Synthesis of N-Bridgehead Azepine Skeletons

Angewandte Chemie (International ed.), 2014-05, Vol.53 (20), p.5142-5146 [Peer Reviewed Journal]

2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;Copyright Wiley Subscription Services, Inc. May 2014 ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201400881 ;PMID: 24700758 ;CODEN: ACIEAY

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18
Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3-Aliphatic-Substituted Indoles and Pyrroles
Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3-Aliphatic-Substituted Indoles and Pyrroles
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Vinyl Moiety as a Handle for Regiocontrol in the Preparation of Unsymmetrical 2,3-Aliphatic-Substituted Indoles and Pyrroles

Angewandte Chemie (International ed.), 2011-02, Vol.50 (6), p.1338-1341 [Peer Reviewed Journal]

Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201006381 ;PMID: 21290507 ;CODEN: ACIEAY

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19
Rhodium(III)-Catalyzed CH Activation of Arenes Using a Versatile and Removable Triazene Directing Group
Rhodium(III)-Catalyzed CH Activation of Arenes Using a Versatile and Removable Triazene Directing Group
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Rhodium(III)-Catalyzed CH Activation of Arenes Using a Versatile and Removable Triazene Directing Group

Angewandte Chemie (International ed.), 2012-07, Vol.51 (29), p.7242-7245 [Peer Reviewed Journal]

Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201203230 ;PMID: 22733572

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20
Developing Chiral Ligands for Asymmetric Hydrogenation
Developing Chiral Ligands for Asymmetric Hydrogenation
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Developing Chiral Ligands for Asymmetric Hydrogenation

Accounts of chemical research, 2007-12, Vol.40 (12), p.1278-1290 [Peer Reviewed Journal]

Copyright © 2007 American Chemical Society ;ISSN: 0001-4842 ;EISSN: 1520-4898 ;DOI: 10.1021/ar7000028 ;PMID: 17506517

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