2010
DOI: 10.1016/j.tet.2010.07.064
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Another mode of heterocyclization of an enantiopure C2-symmetric bis-epoxide leading to the symmetric dialkyl sulfide

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Cited by 5 publications
(1 citation statement)
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“…To create fused tricyclic oxepines, palladium-catalyzed oligocyclizations were employed (29).Xie et al reported the synthesis of thiepin derivatives, sulphides react with alkyl and aryl bis electrophiles. Enantiopure C2-symmetric bisepoxide 29 was demonstrated to interact with sodium sulphide nonahydrate to form the chiral polyhydroxylated thiepane 30, or, by a chemoselective heterocyclization process(30). Saito et al reported Dibenzo[b,f]thiepine 32 was synthesised via an SNAr-isomerization-SNAr sequence involving dichlorostilbene 31 and the same sulfuric acid reagent(31).Another synthetic method has been brought to light by Boutillier et al by using radical addition method in which there is a transfer of xanthates 33 with alkenes.…”
mentioning
confidence: 99%
“…To create fused tricyclic oxepines, palladium-catalyzed oligocyclizations were employed (29).Xie et al reported the synthesis of thiepin derivatives, sulphides react with alkyl and aryl bis electrophiles. Enantiopure C2-symmetric bisepoxide 29 was demonstrated to interact with sodium sulphide nonahydrate to form the chiral polyhydroxylated thiepane 30, or, by a chemoselective heterocyclization process(30). Saito et al reported Dibenzo[b,f]thiepine 32 was synthesised via an SNAr-isomerization-SNAr sequence involving dichlorostilbene 31 and the same sulfuric acid reagent(31).Another synthetic method has been brought to light by Boutillier et al by using radical addition method in which there is a transfer of xanthates 33 with alkenes.…”
mentioning
confidence: 99%