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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Theoretical and applied genetics 63 (1982), S. 177-181 
    ISSN: 1432-2242
    Schlagwort(e): Cytogenetics ; Interspecific hybrid ; Nicotiana debneyi ; N. umbratica ; Colchiploids
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary Interspecific F1 hybrids of Nicotiana debneyi Domin (2n=48) and N. umbratica Burbidge (2n=46), both belonging to the section Suaveolentes, showed a high degree of meiotic chromosome pairing. Two of the five F2 plants obtained exhibited chromosome mosaicism. The first colchiploid generation (C1) had the expected chromosome number of 2n=94 while C2 showed 2n=88, a loss of three pairs of chromosomes. This same chromosome number continued in further colchiploid generations, followed up to C5, except for a few plants in C3 which showed chromosome mosaicism. The F1 phenotype was stable through C1 to C5 and fertility was normal in colchiploids through all generations in spite of the loss of three pairs of chromosomes and chromosome mosaicism. This stability and fertility apparently reflect the tolerance of the genomes to the genetic adjustment of chromosome complements which is believed to be associated with the originally polyploid nature of the parental species and the chromosome doubling brought about in the amphidiploids.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Amino acids 6 (1994), S. 97-105 
    ISSN: 1438-2199
    Schlagwort(e): Amino acids ; Chirospecific ; D-Glucosamine hydrochloride ; D-Mannosamine hydrochloride ; L-N-t-Butyloxycarbonylserinal ; D-N-t-Butyloxycarbonylserinal ; D-p-Chlorohomophenylalanine N-t-Boc DCHA salt ; L-p-Chlorohomophenylalanine N-t-Boc DCHA salt
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The chirospecific conversions of D-glucosamine hydrochloride and D-mannosamine hydrochloride to the configurationally stable L and D isomers of N-t-butyloxycarbonylserinal were carried out byt-butylcarbonylation followed by sodium borohydride reduction and sodium meta-periodate oxidation. Reaction of the L and D aldehydes with the Wittig reagent prepared from 4-chlorobenzyltriphenylphosphonium chloride and butyl lithium followed by catalytic hydrogenation, Jones oxidation and salt formation with dicyclohexylamine gave the DCHA salts of the D and L isomers ofp-chlorohomophenylalanine N-t-Boc in high enatiomeric excess. The optical purity of the title compounds was established by hydrolysis to the respective free amino acids, followed by chiral derivatization and HPLC analysis.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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