226885-93-4

Upstream product

• 72904-78-0 methyl 3-deoxy-4,6-O-phenylmethylene-α-D-arabinohexopyranoside 
• 226885-92-3 (4S,6R)-4-<(4-methoxybenzyl)oxy>-6-<(methoxymethyl)oxy>-2-cyclohexene-1-one 
• 226885-87-6 methyl 4,6-O-benzylidene-3-deoxy-2-O-(4-methoxybenzyl)-α-D-arabinopyranoside 
• 226885-89-8 methyl 3,6-dideoxy-6-iodo-2-O-(4-methoxybenzyl)-4-O-methoxymethyl-α-D-arabinopyranoside 
• 226885-90-1 methyl 3,6-dideoxy-2-O-(4-methoxybenzyl)-4-O-methoxymethyl-α-D-threo-hex-5-enopyranoside 
• 748154-80-5 (2S,4S)-5-Hydroxy-4-(4-methoxy-benzyloxy)-2-methoxymethoxy-cyclohexanone 
• 226885-88-7 methyl 3-deoxy-2-O-(4-methoxybenzyl)-α-D-arabinopyranoside 
• 748154-79-2 (2S,3S,5S,6S)-2-Iodomethyl-6-methoxy-5-(4-methoxy-benzyloxy)-tetrahydro-pyran-3-ol 
• 226885-91-2 (4S,6S)-4-<(4-methoxybenzyl)oxy>-6-<(methoxymethyl)oxy>-2-cyclohexene-1-one 

Downstream Products

• 226885-96-7 (3S,4S,6R)-3-<(N,N-dimethylaminocarbonyl)methyl>-4-<(4-methoxybenzyl)oxy>-6-<(methoxymethyl)oxy>-cyclohexene 
• 21764-32-9 (+)-paniculide A 
• 162599-60-2 (1aR,2aS,5S,5aS,6S,6aS)-2,2a,5,5a,6,6a-hexahydro-1a-methyl-5-(4-methyl-3-pentenyl)-5-phenylseleno-6-<(triethylsilyl)oxy>oxirenobenzofuran-4(1aH)-one 
• 226885-99-0 (3aR,4S,6R,7S,7aR)-4-<(4-methoxybenzyl)oxy>-6-<(methoxymethyl)oxy>-3a,4,5,6,7,7a-hexahydrobenzofuran-2(3H)-one 
• 226885-97-8 (3aR,4S,6R,7S,7aR)-7-iodo-4-<(methoxybenzyl)oxy>-6-<(methoxymethyl)oxy>-3a,4,5,6,7,7a-hexahydrobenzofuran-2(3H)-one 
• 226886-01-7 (3S,3aR,4S,6R,7aS)-6-hydroxy-4-<(4-methoxybenzyl)oxy>-3-(4-methyl-3-pentenyl)-3a,4,5,6,7,7a-hexahydrobenzofuran-2(3H)-one 
• 226886-00-6 (3S,3aR,4S,6R,7aR)-4-<(4-methoxybenzyl)oxy>-6-<(methoxymethyl)oxy>-3-(4-methyl-3-pentenyl)-3a,4,5,6,7,7a-hexahydrobenzofuran-2(3H)-one 
• 226886-02-8 (3S,3aR,4S,6R,7aS)-6-<(methanesulfonyl)oxy>-4-<(4-methoxybenzyl)oxy>-3-(4-methyl-3-pentenyl)-3a,4,5,6,7,7a-hexahydrobenzofuran-2(3H)-one 

Relevant academic research and scientific papers

Total synthesis of paniculide a from D-glucose

The chiral total synthesis of paniculide A (1), a highly oxygenated sesquiterpene possessing a bisabolane skeleton, starting from D-glucose is described. The two different approaches, both involved Ferrier's carbocyclization reaction to construct the cycl