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Refinado por: Nome da Publicação: Journal Of Organic Chemistry remover assunto: Molecular Structure remover
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Electrochemical Selenylative Carbannulation of Biaryl Ynones to Seleno-Dibenzocycloheptenones/Spiro[5.5]Trienones
Electrochemical Selenylative Carbannulation of Biaryl Ynones to Seleno-Dibenzocycloheptenones/Spiro[5.5]Trienones
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Electrochemical Selenylative Carbannulation of Biaryl Ynones to Seleno-Dibenzocycloheptenones/Spiro[5.5]Trienones

Raji Reddy, Chada ; Kolgave, Dattahari H

Journal of organic chemistry, 2021-12, Vol.86 (23), p.17071-17081 [Periódico revisado por pares]

United States: American Chemical Society

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2
Direct Electrochemical Selenylation/Cyclization of Alkenes: Access to Functionalized Benzheterocycles
Direct Electrochemical Selenylation/Cyclization of Alkenes: Access to Functionalized Benzheterocycles
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Direct Electrochemical Selenylation/Cyclization of Alkenes: Access to Functionalized Benzheterocycles

Cheng, Xiaomei ; Hasimujiang, Balati ; Xu, Zhongnan ; Cai, Haiping ; Chen, Guihong ; Mo, Guangquan ; Ruan, Zhixiong

Journal of organic chemistry, 2021-11, Vol.86 (22), p.16045-16058 [Periódico revisado por pares]

United States: American Chemical Society

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3
Cross-Electrophile Coupling: Principles of Reactivity and Selectivity
Cross-Electrophile Coupling: Principles of Reactivity and Selectivity
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Cross-Electrophile Coupling: Principles of Reactivity and Selectivity

Everson, Daniel A ; Weix, Daniel J

Journal of organic chemistry, 2014-06, Vol.79 (11), p.4793-4798 [Periódico revisado por pares]

United States: American Chemical Society

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4
Developing Ligands for Palladium(II)-Catalyzed C–H Functionalization: Intimate Dialogue between Ligand and Substrate
Developing Ligands for Palladium(II)-Catalyzed C–H Functionalization: Intimate Dialogue between Ligand and Substrate
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Developing Ligands for Palladium(II)-Catalyzed C–H Functionalization: Intimate Dialogue between Ligand and Substrate

Engle, Keary M ; Yu, Jin-Quan

Journal of organic chemistry, 2013-09, Vol.78 (18), p.8927-8955 [Periódico revisado por pares]

United States: American Chemical Society

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5
Three Unusual Sesquiterpenes with Distinctive Ring Skeletons from Daphne penicillata Uncovered by Molecular Networking Strategies
Three Unusual Sesquiterpenes with Distinctive Ring Skeletons from Daphne penicillata Uncovered by Molecular Networking Strategies
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Three Unusual Sesquiterpenes with Distinctive Ring Skeletons from Daphne penicillata Uncovered by Molecular Networking Strategies

Zhao, Peng ; Li, Zhi-Yuan ; Qin, Shu-Yan ; Xin, Ben-Song ; Liu, Yu-Yang ; Lin, Bin ; Yao, Guo-Dong ; Huang, Xiao-Xiao ; Song, Shao-Jiang

Journal of organic chemistry, 2021-11, Vol.86 (21), p.15298-15306 [Periódico revisado por pares]

United States: American Chemical Society

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6
Cobalt-Catalyzed C–H Arylations, Benzylations, and Alkylations with Organic Electrophiles and Beyond
Cobalt-Catalyzed C–H Arylations, Benzylations, and Alkylations with Organic Electrophiles and Beyond
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Cobalt-Catalyzed C–H Arylations, Benzylations, and Alkylations with Organic Electrophiles and Beyond

Ackermann, Lutz

Journal of organic chemistry, 2014-10, Vol.79 (19), p.8948-8954 [Periódico revisado por pares]

United States: American Chemical Society

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7
Applying Flow Chemistry: Methods, Materials, and Multistep Synthesis
Applying Flow Chemistry: Methods, Materials, and Multistep Synthesis
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Applying Flow Chemistry: Methods, Materials, and Multistep Synthesis

McQuade, D. Tyler ; Seeberger, Peter H

Journal of organic chemistry, 2013-07, Vol.78 (13), p.6384-6389 [Periódico revisado por pares]

United States: American Chemical Society

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8
Recent Advances in Asymmetric Catalytic Methods for the Formation of Acyclic α,α-Disubstituted α‑Amino Acids
Recent Advances in Asymmetric Catalytic Methods for the Formation of Acyclic α,α-Disubstituted α‑Amino Acids
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Recent Advances in Asymmetric Catalytic Methods for the Formation of Acyclic α,α-Disubstituted α‑Amino Acids

Metz, Alison E ; Kozlowski, Marisa C

Journal of organic chemistry, 2015-01, Vol.80 (1), p.1-7 [Periódico revisado por pares]

United States: American Chemical Society

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9
Binaphthyl-Proline Hybrid Chiral Ligands: Modular Design, Synthesis, and Enantioswitching in Cu(II)-Catalyzed Enantioselective Henry Reactions
Binaphthyl-Proline Hybrid Chiral Ligands: Modular Design, Synthesis, and Enantioswitching in Cu(II)-Catalyzed Enantioselective Henry Reactions
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Binaphthyl-Proline Hybrid Chiral Ligands: Modular Design, Synthesis, and Enantioswitching in Cu(II)-Catalyzed Enantioselective Henry Reactions

Yao, Chao ; Chen, Yaoqi ; Wang, Chao ; Sun, Ruize ; Chang, Haotian ; Jiang, Ruiheng ; Li, Lin ; Wang, Xin ; Li, Yue-Ming

Journal of organic chemistry, 2023-06, Vol.88 (12), p.7651-7659 [Periódico revisado por pares]

United States: American Chemical Society

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10
Selective Synthesis of Diverse Spiro-oxindole-fluorene Derivatives via a DABCO-Promoted Annulation Reaction of Bindone and 3‑Methyleneoxindoles
Selective Synthesis of Diverse Spiro-oxindole-fluorene Derivatives via a DABCO-Promoted Annulation Reaction of Bindone and 3‑Methyleneoxindoles
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Selective Synthesis of Diverse Spiro-oxindole-fluorene Derivatives via a DABCO-Promoted Annulation Reaction of Bindone and 3‑Methyleneoxindoles

Liu, Dan ; Liu, Xueyan ; Sun, Jing ; Yan, Chao-Guo

Journal of organic chemistry, 2021-11, Vol.86 (21), p.14705-14719 [Periódico revisado por pares]

United States: American Chemical Society

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