A Total, Asymmetric Synthesis of 2-Deoxy-L-fucose from Furan
摘要:
The Diels-Alder adduct (+)-l of furan to 1-cyanovinyl (1'S)-camphanate was converted to methyl 3,5-O-diacetyl-2,6-dideoxy-beta-L-lyxo-hexofurano-side ((+)-12), a protected form of 2-deoxy-L-fucose, in 8 steps and 16.6% overall yield.
A Total, Asymmetric Synthesis of 2-Deoxy-L-fucose from Furan
作者:Durgnat、Warm、Vogel
DOI:10.1080/00397919208021319
日期:1992.7
The Diels-Alder adduct (+)-l of furan to 1-cyanovinyl (1'S)-camphanate was converted to methyl 3,5-O-diacetyl-2,6-dideoxy-beta-L-lyxo-hexofurano-side ((+)-12), a protected form of 2-deoxy-L-fucose, in 8 steps and 16.6% overall yield.