The assembly of architecturally complex alkaloids embedding the indole nucleus is of
paramount importance for the target oriented synthesis of biologically active molecules. 1 A …

The tetrahydro-β-carboline (THBC) nucleus is a predominant feature of a vast array of
naturally occurring alkaloids. Most of these alkaloids have been found to exhibit significant …

The development of cost-effective and sustainable catalytic methods for the production of
enantiomerically pure chiral amines is a key challenge facing the pharmaceutical and fine …

Chiral SPINOL‐phosphoric acids are highly enantioselective catalysts for the asymmetric
Pictet–Spengler reaction of N b‐α‐naphthylmethyl tryptamines with a series of aliphatic and …

Tetrahydro-β-carboline skeletons are prominent and ubiquitous in an extraordinary range of
indole alkaloid natural products and pharmaceutical compounds. Powerful synthetic …

Azomethine ylide annulations: facile access to polycyclic ring systems - Chemical Science (RSC
Publishing) DOI:10.1039/C0SC00432D Royal Society of Chemistry View PDF VersionPrevious …

Erfolgreiches Tandem: In der Titelreaktion isomerisieren Doppelbindungen, die bei der
Ringschlussmetathese erzeugt werden, wobei reaktive Iminiumintermediate entstehen, die …

Stereoselective methods for the synthesis of tetrahydro‐ß‐carbolines are of significant
interest due to the broad spectrum of biological activity of the target molecules. In the plant …

Chiral tetrahydro‐β‐carboline (THβC) is not only a prevailing structural feature of many
natural alkaloids but also a versatile synthetic precursor for a vast array of monoterpenoid …

Metal‐coordinated frameworks derived from small peptidic ligands have received much
attention thanks to peptides' vast structural and functional diversity. Various peptides with …