3412-48-4Relevant academic research and scientific papers
An achiral manganese salen catalyst encapsulated in a peptidic phosphonate homochiral solid for the enantioselective formation of diols by consecutive epoxidation and hydration reactions
Milo, Anat,Neumann, Ronny
supporting information; experimental part, p. 2535 - 2537 (2011/04/26)
An insoluble, porous, amorphous, homochiral material based on a polypeptide titanium-phosphonate scaffold with an encapsulated achiral Mn III-salen was prepared and characterized. Consecutive epoxidation and hydration of styrene and its derivatives by aqueous hypochlorite in THF showed the highly enantioselective (>99%) formation of styrene diol derivatives.
Footprint catalysis. IX. Molecular footprint catalytic cavities imprinted with chiral hydantoins; enantioselective hydantoinase mimics
Matsuishi,Shimada,Morihara
, p. 748 - 756 (2007/10/02)
Imprinting using chiral 5-phenyhydantoins ((5R)- and (5S)-5-pheny-2,4-imidazolinedione) as templates could mark chiral molecular footprint-like cavities on a silica (alumina) gel surface. These cavities displayed evident enantioselective catalyses in reac
New routes to 1,4-benzodiazepin-2,5-diones
Akssira,Boumzebra,Kasmi,Dahdouh,Roumestant,Viallefont
, p. 9051 - 9060 (2007/10/02)
1,4-benzodiazepin-2,5-diones have been synthesized in good overall yields by two routes, the first one by cyclisation of dipeptides prepared from Boc anthranilic acid and α-amino acid methyl esters, the second one by reaction of N-carboxy α-amino acid anhydrides with Boc anthranilic acid.
