𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of enantiomerically pure constrained γ-hydroxy-α-amino acids by directed hydroxylation

✍ Scribed by Alberto Avenoza; Carlos Cativiela; Miguel París; Jesús M. Peregrina; Beatriz Saenz-Torre


Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
512 KB
Volume
8
Category
Article
ISSN
0957-4166

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Synthesis of γ-hydroxy-α-amino acids by
✍ Alberto Avenoza; Carlos Cativiela; Jesús M. Peregrina 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 531 KB

The amide group of y&unsaturated amino acids can be used for the preparation of yhydroxya-amino acids. Product 2, which is easily obtained by hydrolysis of the spiro-oxazoloneadduct formed in the Diels-Alder reaction between (Z)-2-phenyl-4-benzylidene-5(4H)-oxaxolone 1 and 1,3butadiene. was converte

Synthesis of a new type of conformationa
✍ Alberto Avenoza; Carlos Cativiela; Miguel París; Jesús M. Peregrina 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 596 KB

Optically active cis-, 8a and 8b, and trans-l-aminomethyl-2-phenylcyclohexane-1carboxylic acids, 9a and 9b, were obtained starting from 1,3-butadiene using Diels-Alder cycloadditions with chiral (E)-2-cyanocinnamates as key steps and following a protocol of stereocontrolled reactions. Subsequent cyc