Literature DB >> 11073639

Substituted guanidines: introducing diversity in combinatorial chemistry.

M del Fresno1, A El-Faham, L A Carpino, M Royo, F Albericio.   

Abstract

The guanidine moiety is an important motif present in many biologically active compounds. Fully substituted guanidines are of key importance for the development of bioactive molecules. The present paper reports on an efficient procedure for the direct solid-phase conversion of amines to fully substituted guanidines under very mild conditions.

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Year:  2000        PMID: 11073639     DOI: 10.1021/ol006322p

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Solid-phase synthesis of a library of amphipatic hydantoins. Discovery of new hits for TRPV1 blockade.

Authors:  Guillermo Gerona-Navarro; Rosario González-Muñiz; Asia Fernández-Carvajal; José M González-Ros; Antonio Ferrer-Montiel; Cristina Carreño; Fernando Albericio; Miriam Royo
Journal:  ACS Comb Sci       Date:  2011-07-08       Impact factor: 3.784

2.  Investigation of the N-Terminus Amino Function of Arg10-Teixobactin.

Authors:  Shimaa A H Abdel Monaim; Sikabwe Noki; Estelle J Ramchuran; Ayman El-Faham; Fernando Albericio; Beatriz G de la Torre
Journal:  Molecules       Date:  2017-09-28       Impact factor: 4.411

3.  Solid-phase synthesis of new Trp(Nps)-containing dipeptide derivatives as TRPV1 channel blockers.

Authors:  Ma Jesús Pérez de Vega; Ma Teresa García-López; Laura Zaccaro; Miriam Royo; Fernando Albericio; Asia Fernández-Carvajal; Antonio Ferrer-Montiel; Rosario González-Muñiz
Journal:  Molecules       Date:  2010-07-15       Impact factor: 4.411

  3 in total

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