After the carbene precursor is prepared, it can be used to react with an alcohol (methanol in this case) to form the quaternary carbon at the anomeric position. This step is crucial for introducing the sugar moiety into the molecule. The reaction typically occurs under mild conditions, and the carbene reacts with the alcohol to form the desired pyranoside product.
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methyl 4,6-O-benzylidene-2-O-diazoacetyl-3-O-pivaloyl-α-D-mannopyranoside
