Sin carga. Con carga. Grupo amino. Grupo guanidino. Grupo imidazol.

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Example of a chiral center the carbon atom , with the two enantiomers shown. From Wikimedia Commons, the free media repository. File information. Structured data. Captions English Add a one-line explanation of what this file represents.

Summary [ edit ] Description Chiral. You cannot overwrite this file. The following other wikis use this file: Usage on ar. Structured data Items portrayed in this file depicts. Category : Enantiomers. Namespaces File Discussion. Views View Edit History. This page was last edited on 3 June , at Files are available under licenses specified on their description page. All structured data from the file and property namespaces is available under the Creative Commons CC0 License ; all unstructured text is available under the Creative Commons Attribution-ShareAlike License ; additional terms may apply.

By using this site, you agree to the Terms of Use and the Privacy Policy. Description Chiral. Made by myself with the free software program Inkscape. The source code of this SVG is valid. This vector image was created with Inkscape. Public domain Public domain false false. This work has been released into the public domain by its author, I, Isilanes. This applies worldwide. In some countries this may not be legally possible; if so: I, Isilanes grants anyone the right to use this work for any purpose , without any conditions, unless such conditions are required by law.


Compuesto meso

It is further claimed, obtaining R 2-aminoethyl 6,8-difluorochromanyl -1,3-didihidroimidazolthione. Reivindicacion Un proceso para preparar el enantiomero R o S de un compuesto de formula 3 que comprende formar el enantiomero R o S de un compuesto de formula 1 mediante un proceso de acuerdo con cualquiera de las reivindicaciones precedentes, seguido por convertir el enantiomero R o S del compuesto 1 en el respecto enantiomero R o S de un compuesto de formula 3. Claim A process for preparing the R or S enantiomer of a compound of formula 3 comprising forming the R or S enantiomer of a compound of formula 1 by a process according to any of the preceding claims, followed by converting the R or S enantiomer of compound 1 in the R or S enantiomer to a compound of formula 3. Reivindicacion El compuesto de formula 1 , estando el compuesto en la forma del enantiomero R sustancialmente puro, el enantiomero S sustancialmente puro, o una mezcla de los enantiomeros R y S, donde X es CH2, oxigeno o azufre; Claim The use of a chiral catalyst comprising a complex of transition metals comprising a chiral ligand in the asymmetric hydrogenation of a compound of formula 2 wherein X, R1, R2, R3 and R4 have the same meanings as defined in claim 1. USP true


Inducción asimétrica

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