320 likes | 337 Views
Explore the reactivity of heteroaromatic compounds, such as furans, thiophenes, pyrroles, and indoles, through metalation processes. Discover the diverse synthetic uses of metalated compounds in the formation of various heterocycles.
E N D
Synthetic Use of Metalated non-DMG Furans and Thiophenes. Conversions into other Heterocycles
Synthetic Use of Metalated non-DMG Furans and Thiophenes. Oxidative Pathways
Use of Metalated non-DMG Thiophenes. Historical Industrial Practice
Directed ortho Metalation (DoM) Reactivity of Furans and Thiophenes
DoM Chemistry of Furans and Thiophenes. Carbon-Based DMG’s. DMG = 2-oxazolino
DoM Reactivity of Furans and Thiophenes. Dianion Equivalents with Carbon-based DMGs
DoM Reactivity of Furans and Thiophenes. “DMG” = CO2-
DoM Chemistry of Furans and Thiophenes. Heteroatom - Based DMGs, DMG = SO2R
DoM Reactivity of Indoles. N-DMG = CO2t-Bu. Indirect C-7 Substitution
DoM Reactivity of Indoles. Non-N DMG Indoles. DMG = CONR2
DoM Reactivity of Indoles. Non-N DMG Indoles. DMG = CH2NR2
DoM Reactivity of Non-N DMG Indoles. DMG = OCONEt2. Benzenoid Ring Functionalization
DoM Reactivity of p-Excessive Heteroaromatics. Pyrrazoles. N DMGs
DoM Reactivity of Pyrrazoles. Non-N DMGs. DMG = SO2N-R
DoM Reactivity of Pyrrazoles. Total Synthesis Application
DoM Reactivity of Imidazoles. DMG = N-SO2NR2. Silicon Protection
Metalation and DoM Reactivity of Methyl Substituted Oxazoles and Thiazoles