163395-22-0Relevant academic research and scientific papers
A New Access To 14-Membered Macrocycle: Synthesis of Model F-O-G ring of Teicoplanin
Beugelmans, Rene,Bourdet, Sebastien,Zhu, Jieping
, p. 1279 - 1282 (2007/10/02)
A new strategy based upon the intramolecular SNAr reaction was developped for the synthesis of 14-membered macrocycle.The reason for the easy macrocyclisation was advanced and supported by computational studies.
A Convergent Synthesis of 14-Membered F-O-G Ring Analogs of the Teicoplanin Binding Pocket via Intramolecular SNAr Reaction
Zhu, Jieping,Beugelmans, Rene,Bourdet, Sebastien,Chastanet, Jacqueline,Roussi, George
, p. 6389 - 6396 (2007/10/03)
An intramolecular SNAr reaction for efficient macrocyclization via biaryl ether formation was developed for syntheses of the 14-membered macrocycles 2 and 3 related to F-O-G ring of teicoplanin 1.Chloride as well as fluoride could be used as the leaving group in this reaction.However, the latter was prefered since it required milder conditions.Both ortho and para nitro, fluoro disubstituted aromatic rings were suitable for the macrocyclization reaction with tethered aryl oxides.The nonproteinogenic α-amino acid 23, required for the synthesis of 3, was prepared via an asymmetric Strecker synthesis using (R)-phenylglycinol as a chiral auxiliary.The overall synthetic strategy was convergent, and the cyclization could be performed in the presence of the highly sensitive arylglycine unit without racemization.
