Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
The First Example of Azole-Fused Cyclic Anhydride Reacting in the Castagnoli-Cushman Way. / Moreau, Ella; Dar'In, Dmitry; Krasavin, Mikhail.
в: Synlett, Том 29, № 7, st-2017-b0833-l, 23.04.2018, стр. 890-893.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - The First Example of Azole-Fused Cyclic Anhydride Reacting in the Castagnoli-Cushman Way
AU - Moreau, Ella
AU - Dar'In, Dmitry
AU - Krasavin, Mikhail
PY - 2018/4/23
Y1 - 2018/4/23
N2 - Pyrazole-fused cyclic anhydrides have been employed for the first time as the Castagnoli-Cushman reaction partners to produce hitherto unknown 4-oxo-4,5,6,7-tetrahydropyrazolo[1,5- a ]pyrazine-7-carboxylates in remarkably convenient and speedy fashion. Attempts to realize the same chemistry with indole and benzimidazole analogues failed.
AB - Pyrazole-fused cyclic anhydrides have been employed for the first time as the Castagnoli-Cushman reaction partners to produce hitherto unknown 4-oxo-4,5,6,7-tetrahydropyrazolo[1,5- a ]pyrazine-7-carboxylates in remarkably convenient and speedy fashion. Attempts to realize the same chemistry with indole and benzimidazole analogues failed.
KW - Castagnoli-Cushman reaction
KW - cyclic anhydrides
KW - multicomponent reactions
KW - nonstabilized enolate
KW - pyrazole-fused
KW - ANALOGS
UR - http://www.scopus.com/inward/record.url?scp=85042610518&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/first-example-azolefused-cyclic-anhydride-reacting-castagnolicushman-way
U2 - 10.1055/s-0036-1591908
DO - 10.1055/s-0036-1591908
M3 - Article
AN - SCOPUS:85042610518
VL - 29
SP - 890
EP - 893
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 7
M1 - st-2017-b0833-l
ER -
ID: 34633378