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Refinado por: Nome da Publicação: Angewandte Chemie remover assunto: Chemical Synthesis remover
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1
Unclicking the Click: Metal‐Assisted Mechanochemical Cycloreversion of Triazoles Is Possible
Unclicking the Click: Metal‐Assisted Mechanochemical Cycloreversion of Triazoles Is Possible
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Unclicking the Click: Metal‐Assisted Mechanochemical Cycloreversion of Triazoles Is Possible

Krupička, Martin ; Dopieralski, Przemyslaw ; Marx, Dominik

Angewandte Chemie International Edition, 2017-06, Vol.56 (27), p.7745-7749 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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2
The Length of a Ubiquitin Chain: A General Factor for Selective Recognition by Ubiquitin‐Binding Proteins
The Length of a Ubiquitin Chain: A General Factor for Selective Recognition by Ubiquitin‐Binding Proteins
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The Length of a Ubiquitin Chain: A General Factor for Selective Recognition by Ubiquitin‐Binding Proteins

Lutz, Joachim ; Höllmüller, Eva ; Scheffner, Martin ; Marx, Andreas ; Stengel, Florian

Angewandte Chemie (International ed.), 2020-07, Vol.59 (30), p.12371-12375 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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3
Unclicking the Click: Metal‐Assisted Mechanochemical Cycloreversion of Triazoles Is Possible
Unclicking the Click: Metal‐Assisted Mechanochemical Cycloreversion of Triazoles Is Possible
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Unclicking the Click: Metal‐Assisted Mechanochemical Cycloreversion of Triazoles Is Possible

Krupička, Martin ; Dopieralski, Przemyslaw ; Marx, Dominik

Angewandte Chemie, 2017-06, Vol.129 (27), p.7853-7857 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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4
Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide
Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide
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Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide

Yu, Miao ; Schrock, Richard R. ; Hoveyda, Amir H.

Angewandte Chemie (International ed.), 2015-01, Vol.54 (1), p.215-220 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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5
Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide
Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide
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Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide

Yu, Miao ; Schrock, Richard R. ; Hoveyda, Amir H.

Angewandte Chemie, 2015-01, Vol.127 (1), p.217-222 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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6
Catalytic Atroposelective Synthesis of Axially Chiral Azomethine Imines and Neuroprotective Activity Evaluation
Catalytic Atroposelective Synthesis of Axially Chiral Azomethine Imines and Neuroprotective Activity Evaluation
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Catalytic Atroposelective Synthesis of Axially Chiral Azomethine Imines and Neuroprotective Activity Evaluation

Yang, Qian‐Qian ; Chen, Chen ; Yao, Dahong ; Liu, Wei ; Liu, Bo ; Zhou, Jin ; Pan, Dabo ; Peng, Cheng ; Zhan, Gu ; Han, Bo

Angewandte Chemie, 2024-01, Vol.136 (5), p.n/a [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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7
Stereoretentive Olefin Metathesis: An Avenue to Kinetic Selectivity
Stereoretentive Olefin Metathesis: An Avenue to Kinetic Selectivity
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Stereoretentive Olefin Metathesis: An Avenue to Kinetic Selectivity

Montgomery, T. Patrick ; Ahmed, Tonia S. ; Grubbs, Robert H.

Angewandte Chemie International Edition, 2017-09, Vol.56 (37), p.11024-11036 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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8
Catalysis‐Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester
Catalysis‐Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester
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Catalysis‐Enabled Concise and Stereoselective Total Synthesis of the Tricyclic Prostaglandin D2 Metabolite Methyl Ester

Sims, Hunter S. ; Andrade Horn, Pedro ; Isshiki, Ryota ; Lim, Melissa ; Xu, Yan ; Grubbs, Robert H. ; Dai, Mingji

Angewandte Chemie (International ed.), 2022-01, Vol.61 (5), p.e202115633-n/a [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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9
Asymmetric Synthesis of Spiropyrazolones by Sequential Organo- and Silver Catalysis
Asymmetric Synthesis of Spiropyrazolones by Sequential Organo- and Silver Catalysis
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Asymmetric Synthesis of Spiropyrazolones by Sequential Organo- and Silver Catalysis

Hack, Daniel ; Dürr, Alexander B. ; Deckers, Kristina ; Chauhan, Pankaj ; Seling, Nico ; Rübenach, Lukas ; Mertens, Lucas ; Raabe, Gerhard ; Schoenebeck, Franziska ; Enders, Dieter

Angewandte Chemie (International ed.), 2016-01, Vol.55 (5), p.1797-1800 [Periódico revisado por pares]

Germany: Blackwell Publishing Ltd

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10
Asymmetric Synthesis of Spiropyrazolones by Rhodium‐Catalyzed C(sp2)−H Functionalization/Annulation Reactions
Asymmetric Synthesis of Spiropyrazolones by Rhodium‐Catalyzed C(sp2)−H Functionalization/Annulation Reactions
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Asymmetric Synthesis of Spiropyrazolones by Rhodium‐Catalyzed C(sp2)−H Functionalization/Annulation Reactions

Zheng, Jun ; Wang, Shao‐Bo ; Zheng, Chao ; You, Shu‐Li

Angewandte Chemie International Edition, 2017-04, Vol.56 (16), p.4540-4544 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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