As two coexisting and fast-growing research fields in modern synthetic chemistry, the
merging of organocatalysis and C–H bond functionalization is well foreseeable, and the joint …

C− C bond formation is a fundamental transformation in organic synthesis. The development
of new synthetic methodology could be considered as a way of pursuing a novel method for …

Thieme E-Journals - SynOpen / Full Text DE EN Home Products Journals Books Book Series
Service Library Service Help Contact Portal SynOpen Full-text search Full-text search Author …

Intramolecular Morita–Baylis–Hillman and Rauhut–Currier reactions are important tools
which have constantly grown over several years. This review summarizes and highlights …

A method for the C (sp3)–H alkenylation of N-aryl-tetrahydroisoquinoline (THIQ) has been
developed by the combination of electrooxidation and a copper catalyst. The corresponding …

C (sp3)–H alkenylation of tetrahydroisoquinoline by merging Shono oxidation and the Morita–
Baylis–Hillman reaction is developed, employing 4-dimethylaminopyridine as an …

Asymmetric cross-dehydrogenative coupling (CDC) of C (sp3)–H bonds shows great
potential for rapid and stereoselective construction of C–C bonds and use of molecular …

1, 2, 3, 4-Tetrahydroisoquinoline is one of the most important “privileged scaffolds” present
in natural products. C1-chiral tetrahydroisoquinolines have exhibited a wide variety of …

Chiral N-heterocyclic carbenes (NHCs) have been recently established as powerful
catalysts for enantioselective bond-forming processes via noncovalent interactions. The …

Oxidative Povarov reaction of N-benzylanilines was realized under catalytic radical cation
salt induced conditions. The mechanism studies revealed that a radical intermediate was …