halogenated alkenes Recently Published Documents

Three common pathways of nephrotoxicity induced by halogenated alkenes

Cell Biology and Toxicology ◽

10.1007/s10565-015-9293-x ◽

2015 ◽

Vol 31 (1) ◽

pp. 1-13 ◽

Cited By ~ 16

Author(s):

Patrizia Cristofori ◽

Aisha V. Sauer ◽

Andrea Trevisan

Keyword(s):

ChemInform Abstract: Synthetic Exploitation of Halogenated Alkenes Containing an Electron-Withdrawing Group: Synthesis of α-Chlorohydrazones and Ketene Aminals by Regiospecific Reactions of in situ Generated Imide Chlorides.

ChemInform ◽

10.1002/chin.201435046 ◽

2014 ◽

Vol 45 (35) ◽

pp. no-no

Author(s):

Amac Fatih Tuyun

Keyword(s):

Ketene Aminals ◽

Halogenated Alkenes ◽

Corrigendum to “Synthetic exploitation of halogenated alkenes containing an electron-withdrawing group: synthesis of α-chlorohydrazones and ketene aminals by regiospecific reactions of in situ generated imide chlorides” [Tetrahedron Lett. 55 (2014) 2085–2089]

Tetrahedron Letters ◽

10.1016/j.tetlet.2014.05.114 ◽

2014 ◽

Vol 55 (29) ◽

pp. 4017

Author(s):

Amac Fatih Tuyun

Keyword(s):

Ketene Aminals ◽

Halogenated Alkenes ◽

ChemInform Abstract: Synthetic Exploitation of Halogenated Alkenes Containing Electron-Withdrawing Group (EWG): Access to Valuable 2,4-Dinitrothiophenes via Ring-Closing and Ring-Opening/Ring-Closing Protocols.

ChemInform ◽

10.1002/chin.201416119 ◽

2014 ◽

Vol 45 (16) ◽

pp. no-no

Author(s):

Amac Fatih Tuyun

Keyword(s):

Ring Opening ◽

Halogenated Alkenes ◽

Synthetic exploitation of halogenated alkenes containing an electron-withdrawing group: synthesis of α-chlorohydrazones and ketene aminals by regiospecific reactions of in situ generated imide chlorides

Tetrahedron Letters ◽

10.1016/j.tetlet.2014.02.038 ◽

2014 ◽

Vol 55 (13) ◽

pp. 2085-2089 ◽

Cited By ~ 1

Author(s):

Amac Fatih Tuyun

Keyword(s):

Ketene Aminals ◽

Halogenated Alkenes ◽

Corrigendum to “Synthetic Exploitation of Halogenated Alkenes Containing Electron-Withdrawing Group (EWG): Access to Valuable 2,4-Dinitrothiophenes via Ring-Closing and Ring-Opening/Ring-Closing Protocols” : HETEROCYCLES, 2013, 87, 2589 : DOI: 10.3987/COM-13-12860

Heterocycles ◽

10.3987/erratum-com-13-12860 ◽

2014 ◽

Vol 89 (8) ◽

pp. 2027

Author(s):

Amac Fatih Tuyun

Keyword(s):

Ring Opening ◽

Halogenated Alkenes ◽

Synthetic exploitation of halogenated alkenes containing EWG: benzotriazole-mediated synthesis of benzoazetines and thermal transformations

RSC Advances ◽

10.1039/c4ra01425a ◽

2014 ◽

Vol 4 (38) ◽

pp. 19640-19645 ◽

Cited By ~ 3

Author(s):

Amac Fatih Tuyun

Keyword(s):

Thermal Transformations ◽

The stable benzoazetines (5a–d) based on nitrovinyl moieties have been synthesizedviatransamination of bisbenzotriazolyl derivatives (2a–c).

Synthetic Exploitation of Halogenated Alkenes Containing Electron-Withdrawing Group (EWG): Access to Valuable 2,4-Dinitrothiophenes via Ring-Closing and Ring-Opening/Ring-Closing Protocols

Heterocycles ◽

10.3987/com-13-12860 ◽

2013 ◽

Vol 87 (12) ◽

pp. 2589 ◽

Cited By ~ 4

Author(s):

Amac Fatih Tuyun

Keyword(s):

Ring Opening ◽

Halogenated Alkenes ◽

Electron attachment to 14 halogenated alkenes and alkanes, 300-600 K

The Journal of Chemical Physics ◽

10.1063/1.4759168 ◽

2012 ◽

Vol 137 (16) ◽

pp. 164306 ◽

Cited By ~ 13

Author(s):

Nicholas S. Shuman ◽

Jeffrey F. Friedman ◽

Thomas M. Miller ◽

A. A. Viggiano

Keyword(s):

Electron Attachment ◽