3-miktoarm star terpolymers using triple click reactions: Diels-Alder, copper-catalyzed azide-alkyne cycloaddition, and nitroxide radical coupling reactions

2011 ◽  
Vol 50 (4) ◽  
pp. 729-735 ◽  
Author(s):  
Ufuk Saim Gunay ◽  
Hakan Durmaz ◽  
Eda Gungor ◽  
Aydan Dag ◽  
Gurkan Hizal ◽  
...  
Keyword(s):  
Nitroxide Radical ◽  
Diels Alder ◽  
Coupling Reactions ◽  
Click Reactions ◽  
Radical Coupling ◽  
Miktoarm Star

Polynorbornene‐ g ‐poly(ethylene oxide) Through the Combination of ROMP and Nitroxide Radical Coupling Reactions

2020 ◽  
Vol 58 (5) ◽  
pp. 645-653 ◽  
Author(s):  
Clémence Nicolas ◽  
Wenhao Zhang ◽  
Émilie Choppé ◽  
Laurent Fontaine ◽  
Véronique Montembault
Keyword(s):  
Ethylene Oxide ◽  
Nitroxide Radical ◽  
Coupling Reactions ◽  
Radical Coupling ◽  
Poly Ethylene Oxide ◽  
Poly Ethylene

Kinetic analysis of nitroxide radical coupling reactions mediated by CuBr

2010 ◽  
Vol 48 (10) ◽  
pp. 2214-2223 ◽  
Author(s):  
Jakov Kulis ◽  
Craig A. Bell ◽  
Aaron S. Micallef ◽  
Michael J. Monteiro
Keyword(s):  
Kinetic Analysis ◽  
Nitroxide Radical ◽  
Coupling Reactions ◽  
Radical Coupling

Postfunctionalization of polyoxanorbornene backbone through the combination of bromination and nitroxide radical coupling reactions

2015 ◽  
Vol 53 (20) ◽  
pp. 2381-2389 ◽  
Author(s):  
Lale Nur Atici ◽  
Erhan Demirel ◽  
Umit Tunca ◽  
Gurkan Hizal ◽  
Hakan Durmaz
Keyword(s):  
Nitroxide Radical ◽  
Coupling Reactions ◽  
Radical Coupling

scholarly journals Studies on the transannular Diels–Alder reaction of 15-membered macrocyclic trienes containing a trans-trans diene. Part I: Synthesis and isomerization of various model cyclopentadecatrienes

1995 ◽  
Vol 73 (10) ◽  
pp. 1675-1694 ◽  
Author(s):  
Dennis G. Hall ◽  
Renate Müller ◽  
Pierre Deslongchamps
Keyword(s):  
Aqueous Media ◽  
Alder Reaction ◽  
Membered Ring ◽  
Diels Alder ◽  
Coupling Reactions ◽  
Diels Alder Reaction ◽  
Trans Diene

The transannular Diels–Alder reaction of 15-membered macrocyclic trienes with a trans-trans-cis (TTC) olefin geometry can lead to A.B.C.[6.6.7] tricyclic products of trans-syn-trans (TST) and cis-syn-cis (CSC) stereochemistry whereas the TTT isomers can produce the trans-anti-cis (TAC) and cis-anti-trans (CAT) tricycles. In order to study the influence of the position (pro-6.6 or pro-6.7) and the nature (alkyl, alkoxymethyl, or formyl) of the dienophile substituent, a set of 10 model cyclopentadecatrienes was prepared. The synthesis of appropriately functionalized trisubstituted dienophile and diene synthons, as well as their coupling reactions affording acyclic precursors, is described in this paper (first in a series of two). A mild and efficient macrocyclization protocol yielded the required methyl- or alkoxymethyl-substituted cyclic substrates. Further transformations led to the formyl-substituted ones. In particular, the TTT macrocycles containing an enal as a dienophile could be completely isomerized to the corresponding TTC thermodynamic isomers in acidic aqueous media. Keywords: transannular, Diels–Alder, 15-membered ring, A.B.C.[6.6.7] tricycles, diterpene.

Room-Temperature, Water-Promoted, Radical-Coupling Reactions of Phenols with tert-Butyl Nitrite

Synlett ◽  
2017 ◽  
Vol 28 (16) ◽  
pp. 2153-2156 ◽  
Author(s):  
Wen-Ting Wei ◽  
Hongze Liang ◽  
Wen-Ming Zhu ◽  
Weida Liang ◽  
Yi Wu ◽  
...  
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Phenol Derivative ◽  
Tert Butyl ◽  
Radical Coupling ◽  
Air Atmosphere ◽  
Cross Coupling Reaction ◽  
Temperature Water

A radical–radical cross-coupling reaction of phenols with tert-butyl nitrite has been developed with the use of water as an additive. This method allows the construction of C–N bonds under an air atmosphere at room temperature, providing the ortho-nitrated phenol derivative in moderate to good yields.

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