Beilstein J. Org. Chem.2013,9, 97–105, doi:10.3762/bjoc.9.13
blocks 34 or 35 was performed by using an automated oligosaccharide synthesizer (Scheme 5, Supporting Information File 1). This synthesizer is an improved version of a recently disclosed synthesizer prototype [20] whereby a separate unit to accommodate aqueouschemistry was added. To avoid cross
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Graphical Abstract
Scheme 1:
Solid-phase synthesis of biopolymers. X represents a reactive site such as an amino group for pepti...
Beilstein J. Org. Chem.2010,6, 1219–1228, doi:10.3762/bjoc.6.140
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Keywords: allyl substituent effect; allyl sulfides; aqueouschemistry; olefin metathesis; protein modifications; Review
Olefin metathesis is one of the most useful chemical transformations for forming carbon–carbon bonds in organic synthesis (Scheme 1) [1][2][3][4]. The broad utility of olefin metathesis
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Graphical Abstract
Scheme 1:
a) Variation of olefin metathesis: CM = cross-metathesis; RCM = ring-closing metathesis; ROM = ring...