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Cover Picture: Divergent Syntheses of Resorcylic Acid Lactones: L‐783277, LL‐Z1640‐2, and Hypothemycin / Synthesis of a Resorcylic Acid Lactone (RAL) Library Using Fluorous‐Mixture Synthesis and Profile of its Selectivity Against a Panel of Kinases (Chem. Eur. J. 43/2009)
Author(s) -
Dakas PierreYves,
Jogireddy Rajamalleswaramma,
Valot Gaëlle,
Barluenga Sofia,
Winssinger Nicolas
Publication year - 2009
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.200990168
Subject(s) - chemistry , combinatorial chemistry
The different faces of chemical biology, synthesis, compound libraries, functional annotation. On the front face of the cube, the synthesis of a resorcyclic acid library is represented as a circuit combining the different library components along the synthetic pathway based on fluorous isolation technology. The top face represents the functional annotation of the library members in the kinome. For details on the synthesis and activities of this library, see the articles by N. Winssinger et al. on pages 11490 ff. and 11498 ff.