42998-44-7Relevant articles and documents
Approaches to the Synthesis of Cytochalasans. Part 3. Synthesis of a Substituted Tetrahydroisoindolinone Moiety Possessing the Same Relative Configuration as Proxiphomin
Schmidlin, Tibur,Zuercher, Werner,Tamm, Christoph
, p. 235 - 250 (1981)
The total synthesis of the tetrahydroisoindolinone moiety corresponding to proxiphomin (1) is described, bearing functional groups for the attachment of the macrocyclic ring.Knoevenagel-Cope condensation of racemic 2-(benzyloxycarbonylamino)-3-phenylpropa
A concise and stereoselective synthesis of threo-γ-hydroxy-L-β-lysine lactone
Misiti, Domenico,Zappia, Giovanni,Delle Monache, Giuliano Delle
, p. 235 - 238 (2007/10/03)
A stereoselective synthesis of threo-γ-hydroxy-β-L-lysine lactone is reported. The threo-amino alcohol functionality is introduced by iodine-mediated cyclocarbamation of the electron poor allylamine 6. The D-phenylalanine was used as starting material as
Amino acids and peptides. XII. Phosphorus in organic synthesis. VIII. Reaction of malonic acid half esters with diphenyl phosphorazidate
Ninomiya,Shioiri,Yamada
, p. 1398 - 1404 (2007/10/08)
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