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1. Metalation of p -Excessive Heteroaromatics. Thermodynamic Acidities of π - Excessive Heteroaromatics. Kinetic Acidities of π - Excessive Heteroaromatics. Synthetic Use of Metalated non-DMG Furans and Thiophenes. Conversions into other Heterocycles.
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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