文摘
N-Furoylated <span class="smallcaps">lspan>-threonine-, serine-, or cysteine-based aminoacetals are coupled with o-aminoketones or aldehydes to offer rapid access to diverse enantiopure polyheterocycles possessing conformationally locked aminoglycoside-containing molecular scaffolds. The key step involves photogeneration of azaxylylenes which undergo [4 + 4] or [4 + 2] cycloadditions to the tethered furoyl pendants.
Keywords:
conformationally locked ribofuranosylamines; enantiopure polyheterocycles; molecular scaffolds; photogeneration of azaxylylenes; [4 + 2] and [4 + 4] photocycloadditions