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Ruthenium-catalyzed ring closing olefin metathesis of non-natural α-amino acids

✍ Scribed by Floris P.J.T. Rutjes; Hans E. Schoemaker


Book ID
104256136
Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
255 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


The use of various enantiopure amino acid-derived diolefins as substrates for the ring closing olefin metathesis reaction (RCM) has been investigated. This reaction has been shown to be an efficient transformation for providing highly functionalized 6-and 7-membered ring amino acids.


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