Reversible oligomerization of 3-aryl-2-cyanothioacrylamides via [2s + 4s] cycloaddition to substituted 3,4-dihydro-2H-thiopyrans

Reversible oligomerization of 3-aryl-2-cyanothioacrylamides via [2s + 4s] cycloaddition to substituted 3,4-dihydro-2H-thiopyrans is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1080/15685551.2015.1058007

P50authorUlrich S. SchubertQ1707155
Martin D. HagerQ42291734
Christine WeberQ59542913
İlknur YıldırımQ91281938
Julia KötteritzschQ114455679
P2093author name stringStefan Bode
P2860cites workA thermally re-mendable cross-linked polymeric materialQ28204547
Mendable polymersQ29012015
Reversible Diels-Alder reactions for the generation of dynamic combinatorial librariesQ31138096
Self-healing materialsQ39838086
Room-temperature healing of a thermosetting polymer using the Diels-Alder reaction.Q43084171
Temperature-dependent size exclusion chromatography for the in situ investigation of dynamic bonding/debonding reactionsQ43620146
Adduct formation in electrospray ionization mass spectrometry II. Benzoic acid derivativesQ44311212
An atom-efficient conjugation approach to well-defined block copolymers using RAFT chemistry and hetero Diels-Alder cycloaddition.Q47657615
Entropy driven chain effects on ligation chemistry.Q55025797
P433issue7
P921main subjectcycloadditionQ898648
P304page(s)627-640
P577publication date2015-07-09
P1433published inDesigned Monomers and PolymersQ50515375
P1476titleReversible oligomerization of 3-aryl-2-cyanothioacrylamides via [2s + 4s] cycloaddition to substituted 3,4-dihydro-2H-thiopyrans
P478volume18

Reverse relations

Q57499514Remendable polymers via reversible Diels-Alder cycloaddition of anthracene-containing copolymers with fullerenescites workP2860

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