Thioamide dianions derived from N-arylmethyl thioamides: Generation and application as carbon nucleophiles adjacent to the nitrogen atom

Articles in the same Issue

1. Preface
2. New vistas in fullerene endohedrals: Functionalization with compounds from main group elements
3. Molecular tweezers for fullerenes
4. Allium chemistry: Use of new instrumental techniques to “see” reactive organosulfur species formed upon crushing garlic and onion
5. Thioamide dianions derived from N-arylmethyl thioamides: Generation and application as carbon nucleophiles adjacent to the nitrogen atom
6. Anodic oxidation of m-terphenyl thio-, seleno- and telluroethers: Lowered oxidation potentials due to chalcogen···π interaction
7. Transition-metal-catalyzed cleavage of carbon–selenium bond and addition to alkynes and allenes
8. Asymmetric synthesis of aminophosphonic acids mediated by chiral sulfinyl auxiliary: Recent advances
9. Synthesis, structures, and aromaticity of phosphole-containing porphyrins and their metal complexes
10. Synthesis of homo- and heterocyclic silanes via intermediates with Si=Si bonds
11. Synthesis and structure of stable 1,2-diaryldisilyne
12. Alternating dialkylsilylene-divinylarene copolymers
13. Iron carbenoid-mediated ylide reactions
14. Heteroatoms moving protons: Synthetic and mechanistic studies of bifunctional organometallic catalysis
15. Polyfluorinated ligand-supported organometallic complexes of copper, silver, and gold
16. Gold-catalyzed synthesis of N,O-heterocycles
17. Asymmetric tandem reactions: New synthetic strategies
18. Explanatory dictionary of key terms in toxicology: Part II (IUPAC Recommendations 2010)
19. Name and symbol of the element with atomic number 112 (IUPAC Recommendations 2010)