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Nature Chemical Biology, ISSN 1552-4450, 2012, Volume 8, Issue 2, pp. 179 - 184
In biology-oriented synthesis, the scaffolds of biologically relevant compound classes inspire the synthesis of focused compound collections enriched in... 
NUCLEOPHOSMIN | COMPLEX | BIOCHEMISTRY & MOLECULAR BIOLOGY | DRUGS | BIOLOGY-ORIENTED SYNTHESIS | INHIBITOR | EFFICIENT | CANCER | Proteins | Cell division | Biosynthesis | Catalysis | Cellular biology | Natural products | Alkaloids | natural products | Transformation | scaffolds | Indole | Centrosomes | Evolution | Supernumerary | Chromosomes | Spindles
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2015, Volume 54, Issue 1, pp. 315 - 317
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2016, Volume 55, Issue 27, pp. 7586 - 7605
Journal Article
Synlett, ISSN 0936-5214, 12/2017, Volume 28, Issue 20, pp. 2918 - 2922
Abstract Guided by the principle of biology-oriented synthesis, a collection of compounds with decahydro-4,8-epoxyazulene scaffold occurring in bioactive... 
letter | biology-oriented synthesis | azulene | cycloaddition | carbonyl ylides | rhodium | SESQUITERPENES | 4+3 CYCLOADDITION REACTION | (-)-ENGLERIN | CHEMISTRY, ORGANIC | DIAZO-COMPOUNDS | CARBONYL-YLIDE | ENGLERIN
Journal Article
Synthesis, ISSN 0039-7881, 01/2017, Volume 49, Issue 1, pp. 87 - 95
Abstract A biology-oriented synthesis of 3,3-spiro(2-tetrahydrofuranyl)oxindole derivatives is realized through the rhodium(II)-catalyzed three-component... 
paper | biology-oriented synthesis | multicomponent reactions | spirooxindoles | cycloaddition | carbonyl ylides | rhodium | 1,3-DIPOLAR CYCLOADDITIONS | ENANTIOSELECTIVE SYNTHESIS | ONE-POT SYNTHESIS | DIOXOLANES | 3-COMPONENT REACTION | CHEMISTRY, ORGANIC | ACID-A | MOLECULES
Journal Article