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Asymmetric Domino Aza-Michael Addition/[3+2] Cycloaddition Reactions as a Versatile Approach to alpha,beta,gamma,-Triamino Acid Derivatives

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F14%3A10277920" target="_blank" >RIV/00216208:11310/14:10277920 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/14:00427700

  • Result on the web

    <a href="http://dx.doi.org/10.1021/ol403660w" target="_blank" >http://dx.doi.org/10.1021/ol403660w</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/ol403660w" target="_blank" >10.1021/ol403660w</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Asymmetric Domino Aza-Michael Addition/[3+2] Cycloaddition Reactions as a Versatile Approach to alpha,beta,gamma,-Triamino Acid Derivatives

  • Original language description

    Nonproteinogenic amino acids are prepared by an unprecedented domino aza-Michael addition-1,3-dipolar cycloaddition, leading to enantiopure highly substituted pyrrolidinopyrazolines. Nonaflyl azide serves as highly effective diazo transfer reagent, forming the link between the conjugate addition and cycloaddition steps. The resulting pyrrolidinopyrazolines can be rapidly transformed to either alpha,beta,gamma-triamino acids or 3,4-methano-beta-prolines. Peptide coupling can be regioselectively conductedat each of the amino groups.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Organic Letters

  • ISSN

    1523-7060

  • e-ISSN

  • Volume of the periodical

    16

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    4

  • Pages from-to

    1088-1091

  • UT code for WoS article

    000331926800015

  • EID of the result in the Scopus database