A Concise Enantioselective Synthesis of (+)-L-733,060 and (+)-T-2328 via Sequential Proline Catalysis

The development of facile synthetic methods for stereodefined aliphatic cyclic amines is an important research field in synthetic organic chemistry since such scaffolds constitute a variety of natural products and biologically active compounds. N‐Acyl cyclic N,O‐acetals which prepared by electrochemical oxidation of the corresponding cyclic amines have proven to be useful and versatile precursors for the synthesis of such skeletons. In this Personal Account, we introduce our efforts toward the development of synthetic strategies for the diastereo‐ and/or enantioselective synthesis of cyclic amines by using electrochemically prepared cyclic N,O‐acetals. In addition, the investigation of the “memory of chirality” in the electrooxidative methoxylation of N‐acyl amino acid derivatives, the strategy for the synthesis of chiral azabicyclic compounds by utilizing electrochemical oxidation, and halogen cation‐mediated synthesis of nitrogen‐containing heterocycles are also described.

show abstract

Organocatalyzed α-aminooxylation/amination of aldehydes and their sequential reactions: A versatile tool for the synthesis of bioactive molecules

Ahuja

Sudalai

2020

Bioactive Natural Products

View full text Add to dashboard Cite

A Concise Enantioselective Synthesis of (+)-L-733,060 and (+)-T-2328 via Sequential Proline Catalysis

Cited by 6 publications

References 7 publications

ChemInform Abstract: A Concise Enantioselective Synthesis of (+)‐L‐733,060 and (+)‐T‐2328 via Sequential Proline Catalysis.

ChemInform Abstract: A Concise Enantioselective Synthesis of (+)‐L‐733,060 and (+)‐T‐2328 via Sequential Proline Catalysis.

Shono‐Type Oxidation for Functionalization of N‐Heterocycles

Organocatalyzed α-aminooxylation/amination of aldehydes and their sequential reactions: A versatile tool for the synthesis of bioactive molecules

Contact Info

Product

Resources

About