ChemInform Abstract: A Metal-Free Cross-Dehydrogenative Coupling of N-Carbamoyl Tetrahydroisoquinoline by Sodium Persulfate.

10.1002/chin.201441166 ◽

2014 ◽

Vol 45 (41) ◽

pp. no-no

Author(s):

Wenfang Chen ◽

Hongbo Zheng ◽

Xinhui Pan ◽

Zhiyu Xie ◽

Xin Zan ◽

...

Keyword(s):

Sodium Persulfate ◽

Dehydrogenative Coupling

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A metal-free cross-dehydrogenative coupling of N-carbamoyl tetrahydroisoquinoline by sodium persulfate

Tetrahedron Letters ◽

10.1016/j.tetlet.2014.03.094 ◽

2014 ◽

Vol 55 (17) ◽

pp. 2879-2882 ◽

Author(s):

Wenfang Chen ◽

Hongbo Zheng ◽

Xinhui Pan ◽

Zhiyu Xie ◽

Xin Zan ◽

...

Keyword(s):

Sodium Persulfate ◽

Dehydrogenative Coupling

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Latest Advancements in Transition‐Metal‐Free Carbon‐Heteroatom Bond Formation Reactions via Cross‐ Dehydrogenative Coupling

Asian Journal of Organic Chemistry ◽

10.1002/ajoc.202100070 ◽

2021 ◽

Author(s):

Aanchal Batra ◽

Pushpinder Singh ◽

Kamal Nain Singh

Keyword(s):

Transition Metal ◽

Bond Formation ◽

Free Carbon ◽

Dehydrogenative Coupling ◽

Bond Formation Reactions

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Synthesis of Polycyclic Amines through Mild Metal-Free Tandem Cross-Dehydrogenative Coupling/Intramolecular Hydroarylation ofN-Aryltetrahydroisoquinolines and Crotonaldehyde

European Journal of Organic Chemistry ◽

10.1002/ejoc.201403375 ◽

2014 ◽

Vol 2015 (3) ◽

pp. 468-473 ◽

Author(s):

Xiang Wu ◽

Dian-Feng Chen ◽

Shu-Sen Chen ◽

Yi-Fan Zhu

Keyword(s):

Dehydrogenative Coupling

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ChemInform Abstract: Di-tert-butyl Peroxide (DTBP) Promoted Dehydrogenative Coupling: An Expedient and Metal-Free Synthesis of Oxindoles via Intramolecular C(sp2)-H and C(sp3)-H Bond Activation.

10.1002/chin.201604106 ◽

2016 ◽

Vol 47 (4) ◽

pp. no-no

Author(s):

Biplab Mondal ◽

Brindaban Roy

Keyword(s):

Bond Activation ◽

Dehydrogenative Coupling ◽

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ChemInform Abstract: Metal Free TBHP-Promoted Intramolecular Carbonylation of Arenes via Radical Cross-Dehydrogenative Coupling: Synthesis of Indenoquinolinones, 4-Azafluorenones and Fluorenones.

10.1002/chin.201646027 ◽

2016 ◽

Vol 47 (46) ◽

Author(s):

Kalpana Mishra ◽

Ashok Kumar Pandey ◽

Jay Bahadur Singh ◽

Radhey M. Singh

Keyword(s):

Dehydrogenative Coupling

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Metal-Free Visible-Light-Induced C–H/C–H Cross-Dehydrogenative-Coupling of Quinoxalin-2(H)-ones with Simple Ethers

ACS Sustainable Chemistry & Engineering ◽

10.1021/acssuschemeng.8b04652 ◽

2018 ◽

Vol 6 (12) ◽

pp. 17252-17257 ◽

Author(s):

Wei Wei ◽

Leilei Wang ◽

Huilan Yue ◽

Pengli Bao ◽

Weiwei Liu ◽

...

Keyword(s):

Visible Light ◽

Dehydrogenative Coupling

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ChemInform Abstract: DIAD-Mediated Metal-Free Cross Dehydrogenative Coupling Between Tertiary Amines and α-Fluorinated Sulfones.

10.1002/chin.201344089 ◽

2013 ◽

Vol 44 (44) ◽

pp. no-no

Author(s):

Weizhou Huang ◽

Chuanfa Ni ◽

Yanchuan Zhao ◽

Jinbo Hu

Keyword(s):

Tertiary Amines ◽

Dehydrogenative Coupling

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Visible-Light-Mediated Cross Dehydrogenative Coupling of Thiols with Aldehydes: Metal-Free Synthesis of Thioesters at Room Temperature

The Journal of Organic Chemistry ◽

10.1021/acs.joc.1c02111 ◽

2021 ◽

Author(s):

Vishal Jyoti Roy ◽

Partha Pratim Sen ◽

Sudipta Raha Roy

Keyword(s):

Visible Light ◽

Room Temperature ◽

Dehydrogenative Coupling

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Sodium persulfate-promoted site-selective synthesis of mononitroarylamines under transition-metal-free conditions

Tetrahedron ◽

10.1016/j.tet.2019.01.011 ◽

2019 ◽

Vol 75 (9) ◽

pp. 1157-1165

Author(s):

De-Xun Xie ◽

Hui-Juan Yu ◽

Hui Liu ◽

Wei-Cai Xue ◽

Yuan-Shou Qin ◽

...

Keyword(s):

Transition Metal ◽

Selective Synthesis ◽

Sodium Persulfate ◽

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Nitrosonium ion catalysis: aerobic, metal-free cross-dehydrogenative carbon–heteroatom bond formation

Chemical Communications ◽

10.1039/c8cc08328b ◽

2018 ◽

Vol 54 (92) ◽

pp. 13022-13025 ◽

Author(s):

Luis Bering ◽

Laura D’Ottavio ◽

Giedre Sirvinskaite ◽

Andrey P. Antonchick

Keyword(s):

Bond Formation ◽

Environmentally Benign ◽

Reaction Conditions ◽

Dehydrogenative Coupling ◽

Nitrosonium Ion

Catalytic cross-dehydrogenative coupling of heteroarenes with thiophenols and phenothiazines has been developed under mild and environmentally benign reaction conditions.

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