One Diels-Alder adduct of furan to 1-cyanovinyl acetate is converted to 8-oxabicyclo[3,2,1] oct-6-en-2-one which is transformed into beta-C-hexopyranosides including 2-deoxy and 2,3-unsaturated derivatives
A highly stereocontrolled synthesis of a beta-D-ribo-hept-6-ulopyranosuronamide derivative, a useful...
Zinc iodide‐catalyzed cycloaddition of furan to 1‐cyanovinyl (1′S)‐camphanate or 1‐cyanovinyl (1′R)‐...
A simple and effective method for the synthesis of 7-oxabicyclo[2.2.1] heptanes and 8-oxabicyclo[3.2...
(1R,2R,4R)-2-exo-Cyano-7-oxabicyclo[2.2.1]hept-5-en-2-yl (1S)-camphanate [1, Diels Alder adduct of f...
The Diels-Alder adduct (-)-5 (a "naked sugar") of furan to 1-cyanovinyl (1R')-camphanate was convert...
The "naked sugar" (+)-(1R,2S,4R)-2-cyano-7-oxa-bicyclo[2.2.1]hept-5-en-2-yl (1S)-camphanate [(+)-3] ...
Two new deoxycarbaheptopyranoses, 5a-carba-6-deoxy-alpha-DL-galacto-heptopyranose and 5a-carba-6-deo...
Since the initial report by Diels and Alder in 1928, the [4+2] cycloaddition remains one of the most...
The [4+2] cycloaddition leads to rapid formation of molecular complexity that can be achieved in a s...
The racemic 7-oxanorborn-5-en-2-one has been converted into 1,5-anhydro-3-deoxy-3-[1'-(alpha-furyl)-...
The Oshima-Nozaki (Et2AlI) condensation of isolevoglucosenone (4) with 2,6-anhydro-3,4,5,7-tetra-O-b...
Cycloaddition of 1,3-dibromo-2-oxyallyl cation to 2-(benzyloxymethyl)furan provided a 8-oxabicyclo[3...
A new stereocontrolled synthesis of BETA-D-mannopyranosides was defined relying on a high yielding s...
A few novel furanylalkyl hex- and pentenopyranones have been synthesized from the corresponding hexe...
A highly stereocontrolled synthesis of a beta-D-ribo-hept-6-ulopyranosuronamide derivative, a useful...
A highly stereocontrolled synthesis of a beta-D-ribo-hept-6-ulopyranosuronamide derivative, a useful...
Zinc iodide‐catalyzed cycloaddition of furan to 1‐cyanovinyl (1′S)‐camphanate or 1‐cyanovinyl (1′R)‐...
A simple and effective method for the synthesis of 7-oxabicyclo[2.2.1] heptanes and 8-oxabicyclo[3.2...
(1R,2R,4R)-2-exo-Cyano-7-oxabicyclo[2.2.1]hept-5-en-2-yl (1S)-camphanate [1, Diels Alder adduct of f...
The Diels-Alder adduct (-)-5 (a "naked sugar") of furan to 1-cyanovinyl (1R')-camphanate was convert...
The "naked sugar" (+)-(1R,2S,4R)-2-cyano-7-oxa-bicyclo[2.2.1]hept-5-en-2-yl (1S)-camphanate [(+)-3] ...
Two new deoxycarbaheptopyranoses, 5a-carba-6-deoxy-alpha-DL-galacto-heptopyranose and 5a-carba-6-deo...
Since the initial report by Diels and Alder in 1928, the [4+2] cycloaddition remains one of the most...
The [4+2] cycloaddition leads to rapid formation of molecular complexity that can be achieved in a s...
The racemic 7-oxanorborn-5-en-2-one has been converted into 1,5-anhydro-3-deoxy-3-[1'-(alpha-furyl)-...
The Oshima-Nozaki (Et2AlI) condensation of isolevoglucosenone (4) with 2,6-anhydro-3,4,5,7-tetra-O-b...
Cycloaddition of 1,3-dibromo-2-oxyallyl cation to 2-(benzyloxymethyl)furan provided a 8-oxabicyclo[3...
A new stereocontrolled synthesis of BETA-D-mannopyranosides was defined relying on a high yielding s...
A few novel furanylalkyl hex- and pentenopyranones have been synthesized from the corresponding hexe...
A highly stereocontrolled synthesis of a beta-D-ribo-hept-6-ulopyranosuronamide derivative, a useful...
A highly stereocontrolled synthesis of a beta-D-ribo-hept-6-ulopyranosuronamide derivative, a useful...
Zinc iodide‐catalyzed cycloaddition of furan to 1‐cyanovinyl (1′S)‐camphanate or 1‐cyanovinyl (1′R)‐...
A simple and effective method for the synthesis of 7-oxabicyclo[2.2.1] heptanes and 8-oxabicyclo[3.2...
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