Cargando…
An intramolecular inverse electron demand Diels–Alder approach to annulated α-carbolines
Intramolecular inverse electron demand cycloadditions of isatin-derived 1,2,4-triazines with acetylenic dienophiles tethered by amidations or transesterifications proceed in excellent yields to produce lactam- or lactone-fused α-carbolines. Beginning with various isatins and alkynyl dienophiles, a p...
Autores principales: | Ma, Zhiyuan, Ni, Feng, Woo, Grace H C, Lo, Sie-Mun, Roveto, Philip M, Schaus, Scott E, Snyder, John K |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388871/ https://www.ncbi.nlm.nih.gov/pubmed/23015831 http://dx.doi.org/10.3762/bjoc.8.93 |
Ejemplares similares
-
An Advanced ‘clickECM’ That Can be Modified by the Inverse‐Electron‐Demand Diels‐Alder Reaction
por: Nellinger, Svenja, et al.
Publicado: (2021) -
Application of the Inverse-Electron-Demand Diels-Alder Reaction for Metabolic Glycoengineering
por: Haiber, Lisa Maria, et al.
Publicado: (2021) -
Synthesis of some novel annulated pyrido[2,3-d]pyrimidines via stereoselective intramolecular hetero Diels–Alder reactions of 1-oxa-1,3-butadienes
por: Deb, Mohit L, et al.
Publicado: (2010) -
Mechanistic studies of an L-proline-catalyzed pyridazine formation involving a Diels–Alder reaction with inverse electron demand
por: Schnell, Anne, et al.
Publicado: (2019) -
Approach Matters: The Kinetics of Interfacial Inverse‐Electron Demand Diels–Alder Reactions
por: Sen, Rickdeb, et al.
Publicado: (2017)