Nazaret Corres scite author profile

Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3-Carboxamide-1,4-benzodiazepin-5-ones. -Starting from azido-or nitrobenzoic acids (I), isocyanides (II), glyoxals (III), and chiral methylbenzyl amine (IV), both diastereomers of benzodiazepinones [(VI) and (VII)] can be synthesized with a reversal of diastereoselectivity using different cyclization. -(PERTEJO, P.; CORRES, N.; TORROBA, T.; GARCIA-VALVERDE*, M.; Org. Lett. 17 (2015) 3, 612-615, http://dx.

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Nazaret Corres

Synthesis of pseudopeptidic (S)-6-amino-5-oxo-1,4-diazepines and (S)-3-benzyl-2-oxo-1,4-benzodiazepines by an Ugi 4CC Staudinger/aza-Wittig sequence

Synthesis of pseudopeptidic [(5H)-6-oxodibenzo[b,f][1,5]diazocine-5-yl]arylglycinamides by an Ugi 4CC/Staudinger/aza-Wittig sequence

Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3-Carboxamide-1,4-benzodiazepin-5-ones

ChemInform Abstract: Reversal of Diastereoselectivity in the Synthesis of Peptidomimetic 3‐Carboxamide‐1,4‐benzodiazepin‐5‐ones.

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