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Protecting groups, allyl-based deprotections complexes

A new protecting group for amines has been studied and used in the first chiral synthesis of anticapsin. The route involves initial bis-allylation to give a base-stable group resistant to nucleophiles, but which can be easily deprotected using the known allyl-to-propenyl isomerization reaction promoted by transition-metal complexes (Scheme 11). [Pg.223]


See other pages where Protecting groups, allyl-based deprotections complexes is mentioned: [Pg.67]    [Pg.67]    [Pg.293]    [Pg.297]    [Pg.95]    [Pg.1430]    [Pg.174]    [Pg.641]    [Pg.21]    [Pg.373]    [Pg.641]   
See also in sourсe #XX -- [ Pg.175 , Pg.176 ]




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Allyl group

Allylation complexes

Base protecting group

Complex allyl

Protected groups deprotection

Protecting group, allyl

Protecting groups, allyl-based deprotections

Protecting groups, deprotection

Protection -deprotection

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