A novel synthetic route of diaza-bridged heterocycles based on natural 3,9-diazabicyclo[3.3.1]non-6-ene scaffold has been accomplished. The synthetic approach consists of a Pictet-Spengler condensation of the l-Dopa-OMe with an appropriate aldehyde, Fmoc-Aa-H, followed by intramolecular lactamization. This approach generated two configurationally distinct products (cis and trans-isomers), increasing the stereochemical diversity of these compounds
Diastereomerically enriched heterocyclic compounds play a significant role in medicinal chemistry an...
The first synthesis of 6-phenyl-2,6-diazabicyclo[3.2.0]heptane 1 and its orthogonally protected prec...
This thesis describes a new approach towards a formal synthesis of the marine natural product diazon...
A novel synthetic route of diaza-bridged heterocycles based on natural 3,9-diazabicyclo[3.3.1]non-6-...
Abstract The compound 5, containing the novel hetero-cycle 2-oxa-4,7-diazabicyclo[3.3.1]non-3-ene, h...
This work suggests a new general synthetic methodology combining organofluorine and heterocyclic che...
While the benzodiazepine drug class has been amongst the most prescribed medication globally since i...
Template Directed C-H Insertion Reactions for Stereocontrolled Synthesis of Heterocycles Orobosa Mar...
A synthesis of hitherto unknown heterocyclic system 1(5)H-1,5-diazacycl[3.3.2]azine-2,4-dione (5) is...
While the benzodiazepine drug class has been amongst the most prescribed medication globally since i...
A domino reaction sequence involving aldol condensation, alkene isomerization, and intramolecular he...
The biological significance of sp3-rich synthetic scaffolds with natural product-like features yet d...
A practical strategy for the synthesis of diazabenz[e]aceanthrylene-based heterocycles is reported. ...
The core structure of a natural product was selected as scaffold for combinatorial library synthesis...
The preparation of bridged benzo[1,5]oxazocines and benzo[1,4]diazepines is demonstrated from simple...
Diastereomerically enriched heterocyclic compounds play a significant role in medicinal chemistry an...
The first synthesis of 6-phenyl-2,6-diazabicyclo[3.2.0]heptane 1 and its orthogonally protected prec...
This thesis describes a new approach towards a formal synthesis of the marine natural product diazon...
A novel synthetic route of diaza-bridged heterocycles based on natural 3,9-diazabicyclo[3.3.1]non-6-...
Abstract The compound 5, containing the novel hetero-cycle 2-oxa-4,7-diazabicyclo[3.3.1]non-3-ene, h...
This work suggests a new general synthetic methodology combining organofluorine and heterocyclic che...
While the benzodiazepine drug class has been amongst the most prescribed medication globally since i...
Template Directed C-H Insertion Reactions for Stereocontrolled Synthesis of Heterocycles Orobosa Mar...
A synthesis of hitherto unknown heterocyclic system 1(5)H-1,5-diazacycl[3.3.2]azine-2,4-dione (5) is...
While the benzodiazepine drug class has been amongst the most prescribed medication globally since i...
A domino reaction sequence involving aldol condensation, alkene isomerization, and intramolecular he...
The biological significance of sp3-rich synthetic scaffolds with natural product-like features yet d...
A practical strategy for the synthesis of diazabenz[e]aceanthrylene-based heterocycles is reported. ...
The core structure of a natural product was selected as scaffold for combinatorial library synthesis...
The preparation of bridged benzo[1,5]oxazocines and benzo[1,4]diazepines is demonstrated from simple...
Diastereomerically enriched heterocyclic compounds play a significant role in medicinal chemistry an...
The first synthesis of 6-phenyl-2,6-diazabicyclo[3.2.0]heptane 1 and its orthogonally protected prec...
This thesis describes a new approach towards a formal synthesis of the marine natural product diazon...