1,721,028 research outputs found

    UNUSUAL SULFUR AND SELENIUM AMINO ACIDS

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    Presentation of synthetic methods for novel, unnatural sulfur and selenium containing amino acid

    Large Scale Homologation of alpha-Amino Acids

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    Presentation of a synthetic procedure for large scale homologation of alpha-amino acid

    Enantiopure b3-amino acids-2,2-d2 via homologation of proteinogenic a-amino acids

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    A procedure for the synthesis of enantiopure β3-amino acids from proteinogenic α-amino acids, developed by our group a few years ago, has been modified to enable the production of C-2 fully deuterated, C-protected β3-amino acids and, even more important, the synthesis of valuable deuterium labelled N(Boc)-protected chiral synthons, such as 2-aminoalcohols, 2-aminoiodides, and β3-amino nitriles

    Real Time RT-PCR and flow cytometry to investigate wheat kernel hardness: role of puroindoline genes and proteins

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    Developing seeds from Triticum aestivum (wheat) cultivars were collected after flowering and analysed for puroindoline a and b gene expression by Real Time RT-PCR. Mature seeds were investigated for the presence and the amount of starch-associated puroindoline a and b proteins by flow cytometry. Puroindoline a gene and protein were found to have a predominant role in controlling wheat kernel hardness

    SURROGATI DEL LEGAME AMMIDICO: NUOVE METODOLOGIE DI SINTESI IN FASE SOLIDA DI TIOMETILENPSEUDOPEPTIDI

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    E' STATA PRESENTATA UNA NUOVA METODOLOGIA SINTETICA PER OTTENERE TIOMETILENPSEUDOPEPTIDI UTILIZZANDO GLI ENANTIOPURI N-FMOC BETA-IODOAMMINE E L'ACIDO TIOGLICOLICO, ANCH'ESSO PROTETTO ALL'ATOMO DI ZOLFO CON IL GRUPPO FMOC

    Emerging Chemistry from alpha-Amino Acid Homologation Intermediates

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    PRESENTATION OF NEW RESULTS CONCERNIG THE SYNTHESIS OF ENANTIOPURE ORTHOGONALLY PROTECTED EITHER S-(AMINOALKYL) OR Se-(AMINOALKYL) ALPHA-AMINO ACIDS FROM BETA-IODOAMINES AND CYSTEINE OR SELENOCYSTINE RESPECTIVELY IN CONCERT WITH THE PROGRESS IN THE SYNTHESIS OF ENANTIOPURE BETA2,3-AMINO ACIDS FROM n-PROTECTED BETA3-AMINO NITRILES

    Novel thiol- and thioether-containing amino acids: cystathionine and homocysteine families

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    Natural L-homocysteine and L,L-cystathionine, along with a series of unnatural analogues, have been prepared from L-aspartic and L-glutamic acid. Manipulation of the protected derivatives provided x-iodoamino acids, which were used in thioalkylation reactions of sulfur nucleophiles, such as the ester of L-cysteine and potassium thioacetate
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