A short review on the synthesis of pyrrolo[3,4-c]coumarins an isolamellarin-B scaffolds
P Patra - Synthetic Communications, 2022 - Taylor & Francis
This review presents a vast body of literature on various synthetic methodology, biological,
and fluorescence activities of pyrrolo [3, 4‑c] coumarins as published during the last 20–30 …
and fluorescence activities of pyrrolo [3, 4‑c] coumarins as published during the last 20–30 …
The molecular diversity scope of oxindole derivatives in organic synthesis
The role of oxindole derivatives is discussed as starting materials in diverse organic
reactions, including two and more components, between the years 2014 until 2020 …
reactions, including two and more components, between the years 2014 until 2020 …
Organocatalysis in 1, 3-Dipolar Cycloaddition Reactions (A Review)
YA Pronina, LA Teglyai, AI Ponyaev, ML Petrov… - Russian Journal of …, 2024 - Springer
One of the promising directions in 1, 3-dipolar cycloaddition is the implementation of these
reactions under organocatalysis conditions, which makes it possible to achieve not only high …
reactions under organocatalysis conditions, which makes it possible to achieve not only high …
A review on recent progress in synthesis and biological activities of spiropyrrolidine and its derivatives
A Rahman, MZ Alam, A Jahan, S Syed… - Journal of Molecular …, 2025 - Elsevier
Spiro heterocyclic compounds, particularly those containing the spiropyrrolidine scaffold, are
widely found in numerous natural alkaloids and are recognized for their exceptional …
widely found in numerous natural alkaloids and are recognized for their exceptional …
Highly diastereoselective synthesis of trifluoromethyl containing spiro [pyrrolidin-3, 2′-oxindoles] from N-2, 2, 2-trifluoroethylsubstituted isatin imines and β, γ …
Y Xiong, XX Han, Y Lu, HJ Wang, M Zhang, XW Liu - Tetrahedron, 2021 - Elsevier
Inspired by the chemistry and biology of fluorine-containing molecules and pyrrolidinyl
spirooxindoles, herein we report a highly diastereoselective [3+ 2] cycloaddition reaction of …
spirooxindoles, herein we report a highly diastereoselective [3+ 2] cycloaddition reaction of …
New Synthetic Approaches to Benzo-Fused Spiro Heterocycles
IZ Musabirov, RR Gataullin - Russian Journal of Organic Chemistry, 2022 - Springer
The review describes syntheses of new benzo-fused spiro heterocycles by reactions of
isatins, oxindoles, and indenoquinoxalines with nitroalkenes, chalcones in the presence of …
isatins, oxindoles, and indenoquinoxalines with nitroalkenes, chalcones in the presence of …
Decarboxylative, Diastereoselective and exo-Selective 1, 3-Dipolar Cycloaddition for Diversity-Oriented Construction of Structural Spiro [Butyrolactone–Pyrrolidine …
DG Guo, Z Li, XX Han, L Zhang, M Zhang, XL Liu - Synlett, 2021 - thieme-connect.com
Inspired by the chemistry and biology of butyrolactones, pyrrolidines, and chromanones, we
successfully developed a simple domino 1, 3-dipolar cycloaddition of homoserine-lactone …
successfully developed a simple domino 1, 3-dipolar cycloaddition of homoserine-lactone …
Учредители: Российская академия наук
ИЗ МУСАБИРОВ, РР ГАТАУЛЛИН - ЖУРНАЛ ОРГАНИЧЕСКОЙ …, 2022 - elibrary.ru
Описан синтез новых спиросочлененных с циклоалканами бензоксазинов из N-тозил-N-
(2-циклоалк-1-ен-1-илфенил)-N'-фенилмочевин. При взаимодействии этих карбамидов …
(2-циклоалк-1-ен-1-илфенил)-N'-фенилмочевин. При взаимодействии этих карбамидов …
Novas reações de cicloadições formais [3+ 3] entre ácidos cumarino-3-carboxílicos e enaminonas na síntese de carbo-E heterociclos polifuncionalizados.
IS Jesus - 2021 - repositorio.ufba.br
Neste trabalho, foi realizado pela primeira vez, o estudo da reatividade de ácidos cumarino-
3-carboxílicos frente à enaminonas cíclicas de cinco membros em reações de cicloadições …
3-carboxílicos frente à enaminonas cíclicas de cinco membros em reações de cicloadições …