Thermal rearrangement of 3-allyloxy-1,2-benzisothiazole 1,1-dioxides: an unusual inversion of products of sigmatropic [3,3]-shift to give the [1,3]-Isomers [PDF]
3-Allyloxy-1,2-benzisothiazole 1,1-dioxides isomerize thermally to give [3,3]- and [1,3]-products 6 of sigmatropic shift, of which the former reacts further to give solely the [1,3 ...
Brigas, Amadeu+4 more
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Tough, high performance, addition-type thermoplastic polymers [PDF]
A tough, high performance polyimide is provided by reacting a triple bond conjugated with an aromatic ring in a bisethynyl compound with the active double bond in a compound containing a double bond activated toward the formation of a Diels-Adler type ...
Pater, Ruth H.
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Low temperature n-butyllithium-induced [3,3]-sigmatropic rearrangement/electrophile trapping reactions of allyl-1,1-dichlorovinyl ethers. Synthesis of β-, γ- and δ-lactones [PDF]
Aaron Christopher+3 more
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New Three‐Step Domino Reaction, “Thiophilic Addition—β‐Elimination of Fluoride—[3,3] Sigmatropic Rearrangement”: Synthesis of α‐Allylic and α,α‐Bis(allylic) α‐Trifluoromethyl Dithioesters. [PDF]
Fabienne Grellepois+3 more
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Competing [2 + 3] and [4 + 3] cycloadditions of C,N-diphenylnitrone with 1,3-dienes. Evidence for thermally nonequilibrated intermediates [PDF]
Baran, Janusz, Mayr, Herbert
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Synthetic utility and reactivity of N-alkynylazoles [PDF]
textThe chemistry of N-alkynylazoles is a newly emerging area of chemistry with particular interest in heterocycle synthesis. Synthetic preparations of this class of molecule have shown an increasing presence in literature, however, the synthetic ...
Gilbreath, Bradford Lynd
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Synthesis of [3a,7a]-Dihydroindoles by a Tandem Arene Cyclopropanation/3,5-Sigmatropic Rearrangement Reaction [PDF]
Sidney M. Wilkerson‐Hill+3 more
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Cover Picture: Hemin Catalyzed Dealkylative Intercepted [2, 3]‐Sigmatropic Rearrangement Reactions of Sulfonium Ylides with 2, 2, 2‐Trifluorodiazoethane (Adv. Synth. Catal. 10/2020) [PDF]
Xiaojing Yan+4 more
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