Synthesis of (Carbo)nucleoside analogues by [3+2] annulation of aminocyclopropanes

Angewandte Chemie - International Edition

Volumn 53, Issue 32, 2014, Pages 8484-8487

  Racine, Sophie ^a   Denanteuil, Florian ^a   Serrano, Eloisa ^a   Waser, Jérôme ^a  

^a EPFL   (Switzerland)

Author keywords

annulation; catalysis; cyclopropanes; nucleosides; stereoselective synthesis

Indexed keywords

CATALYSIS; KETONES; PROPANE; STEREOCHEMISTRY; STEREOSELECTIVITY;

ANNULATION; BIOACTIVE COMPOUNDS; CYCLOPROPANES; DONOR-ACCEPTOR CYCLOPROPANES; NUCLEOSIDE ANALOGUES; NUCLEOSIDE DERIVATIVES; NUCLEOSIDES; STEREOSELECTIVE SYNTHESIS;

BIOMOLECULES;

CYCLOPROPANE DERIVATIVE; NUCLEOSIDE;

CHEMICAL STRUCTURE; CHEMISTRY; CYCLOADDITION; STEREOISOMERISM; SYNTHESIS;

CYCLOADDITION REACTION; CYCLOPROPANES; MOLECULAR STRUCTURE; NUCLEOSIDES; STEREOISOMERISM;

EID: 84905394892     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201404832     Document Type: Article

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58. The stereochemistry of compounds 8e, 8i, and 9a has been determined by X-ray crystallography. CCDC995573, 994735, and 994948 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif. The stereochemistry of the other compounds has been assigned by analogy or NMR experiments. See Supporting Information for further details.