Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Synthesis of Substituted Indole-3-carboxylates by Iron(II)-Catalyzed Domino Isomerization of 3-Alkyl/aryl-4-aryl-5-methoxyisoxazoles. / Bodunov, Vladimir A.; Galenko, Ekaterina E.; Galenko, Alexey V.; Novikov, Mikhail S.; Khlebnikov, Alexander F.
в: Synthesis (Germany), Том 50, № 14, 17.07.2018, стр. 2784-2798.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Synthesis of Substituted Indole-3-carboxylates by Iron(II)-Catalyzed Domino Isomerization of 3-Alkyl/aryl-4-aryl-5-methoxyisoxazoles
AU - Bodunov, Vladimir A.
AU - Galenko, Ekaterina E.
AU - Galenko, Alexey V.
AU - Novikov, Mikhail S.
AU - Khlebnikov, Alexander F.
PY - 2018/7/17
Y1 - 2018/7/17
N2 - The iron(II)-catalyzed domino isomerization of 3-alkyl/aryl-4-arylisoxazoles provides a selective access to a wide range of structurally diverse highly substituted indole-3-carboxylates. The operational simplicity, high atom efficiency, and the use of stable starting materials and an inexpensive and low-toxicity catalyst are some of the attractive features of this tandem double ring-opening-ring-closure strategy.
AB - The iron(II)-catalyzed domino isomerization of 3-alkyl/aryl-4-arylisoxazoles provides a selective access to a wide range of structurally diverse highly substituted indole-3-carboxylates. The operational simplicity, high atom efficiency, and the use of stable starting materials and an inexpensive and low-toxicity catalyst are some of the attractive features of this tandem double ring-opening-ring-closure strategy.
KW - domino reactions
KW - indoles
KW - iron(II) chloride catalysis
KW - isomerization
KW - isoxazoles
UR - http://www.scopus.com/inward/record.url?scp=85048019185&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/synthesis-substituted-indole3carboxylates-ironiicatalyzed-domino-isomerization-3alkylaryl4aryl5metho
U2 - 10.1055/s-0036-1591576
DO - 10.1055/s-0036-1591576
M3 - Article
AN - SCOPUS:85048019185
VL - 50
SP - 2784
EP - 2798
JO - Synthesis
JF - Synthesis
SN - 0039-7881
IS - 14
ER -
ID: 28604588