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Front Cover: Stereospecific Protodeauration/Transmetalation Generating Configurationally Stable P‐Metalated Nucleoside Derivatives (Eur. J. Org. Chem. 19/2018)
Author(s) -
Richard Marcia E.,
Ciccarelli Rosa M.,
Garcia Kevin J.,
Miller Erica J.,
Casino Stephanie L.,
Pike Robert. D.,
Stockland Jr Robert A.
Publication year - 2018
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Reports
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201800672
Subject(s) - transmetalation , chemistry , stereospecificity , front cover , nucleoside , stereochemistry , reactivity (psychology) , metalation , cover (algebra) , organic chemistry , catalysis , mechanical engineering , engineering , medicine , alternative medicine , pathology
The Front Cover shows the generation and reactivity of configurationally stable P‐metallated nucleoside derivatives. The examples shown in this illustration were prepared through a series of stereospecific protodemetalation and transmetalation reactions. The aurated examples were successfully used as substrates in stereospecific base‐free P‐arylation reactions leading to functionalized nucleosides. The authors thank Barbara Stockland for the design of the cover. More information can be found in the Communication by R. A. Stockland Jr et al.