An Alkyne Linchpin Strategy for Drug:Pharmacophore Conjugation: Experimental and Computational Realization of a meta-selective Inverse Sonogashira Coupling

This folder contains the output log files of the study of Pd-catalysed alkynylation entitled "A Linchpin Approach to Access Drug-Pharmacophore Conjugate by Inverse Sonogashira at meta-Position: Experimental and Computational Exploration" The folder structure is organised as below: /0_sm/: starting materials for the reactions /1_alkynylation_of_1b/: alkynylation reaction using substrate 1b, including regioconvergence studies /2_alkynylation_of_1b_aa_ligand/: alkynylation (C-H activation and 1,2-migratory insertion) reaction using MPAA ligand instead of acetate /3_alkynylation_of_1b_copper/: alkynylation involving Cu(OAc)2 additive /4_arene_site_selectivity_ortho_para/: site selectivity studies for C-H activation /5_alternative_oxidative_addition_TSs/: oxidative addition TSs that all have higher activation barriers that 1,2-migratory insertion TSs /6_ethynyltrimethylsilane_1c/: alkynylation reaction using substrate 1c, including regioconvergence studies /7_bromoethynylbenzene_1d/: alkynylation reaction using substrate 1d, including regioconvergence studies /8_other_substrates/: alkynylation reaction using - substrates 1e-1h (TIPS-, TBDMS-, TES-alkynyl bromide and siloxy-substituted alkynyl bromide), - arene substrates 4, 5, 12 having different substituents - substrates for products 17-19 with different DG tether lengths including regioconvergence studies