102367-86-2

Upstream product

• 98-88-4 benzoyl chloride 
• 117212-74-5 2,3-dehydro-4α-methyl-9β-hydroxydihydroagarofuran 
• 102367-84-0 (1R,3R,6S,9R)-3-Hydroxy-6,10,10-trimethyl-2-methylene-11-oxa-tricyclo[7.2.1.0^1,6]dodecan-7-one 
• 102367-85-1 (1R,2S,3R,6S,9R)-3-Hydroxy-2,6,10,10-tetramethyl-11-oxa-tricyclo[7.2.1.0^1,6]dodecan-7-one 
• 102342-22-3 (1S,2R,6R,9S)-2,6,10,10-Tetramethyl-11-oxa-tricyclo[7.2.1.0^1,6]dodec-3-en-7-one 
• 85249-30-5 9-keto-α-agarofuran 
• 117212-74-5 (1S,2R,6S,7S,9R)-2,6,10,10-Tetramethyl-11-oxa-tricyclo[7.2.1.0^1,6]dodec-3-en-7-ol 
• 102367-84-0 3β-hydroxy-9-keto-α-agarofuran 
• 117937-24-3 3β,4β-epoxy-9-keto-α-agarofuran 
• 79367-90-1 9-keto-α-agarofuran 
• 102367-85-1 3β-hydroxy-4α-methyl-9-ketodihydroagarofuran 
• 102342-22-3 2,3-dehydro-4α-methyl-9-ketodihydroagarofuran 

Downstream Products

• 102342-23-4 C₂₂H₂₈O₄ 
• 102342-24-5 Benzoic acid (1R,2S,3R,6R,7R,9S)-3-hydroxy-2,6,10,10-tetramethyl-11-oxa-tricyclo[7.2.1.0^1,6]dodec-4-en-7-yl ester 
• 102342-25-6 Benzoic acid (1S,2R,3R,4S,5R,6S,7S,9R)-3,4,5-trihydroxy-2,6,10,10-tetramethyl-11-oxa-tricyclo[7.2.1.0^1,6]dodec-7-yl ester 
• 102342-26-7 C₂₅H₃₄O₅ 
• 59812-47-4 (+/-)-isocelorbicol 
• 117212-75-6 2α-selenophenyl-3β-hydroxy-4α-methyl-9β-benzoyloxydihydroagarofuran 
• 117212-73-4 1α,2α-O-isopropylidene-3β-hydroxy-4α-methyl-9β-benzoyloxydihydroagarofuran 
• 102342-26-7 1α,2α-O-isopropylidene-4α-methyl-9β-benzoyloxydihydroagarofuran 
• 102342-25-6 1α,2α,3β-trihydroxy-4α-methyl-9β-benzoyloxydihydroagarofuran 
• 102342-24-5 1,2-dehydro-3β-hydroxy-4α-methyl-9β-benzoyloxydihydroagarofuran 
• 88703-20-2 Benzoic acid (6S,7S)-2,6,10,10-tetramethyl-4-oxo-11-oxa-tricyclo[7.2.1.0^1,6]dodec-2-en-7-yl ester 
• 102342-23-4 2β,3β-epoxy-4α-methyl-9β-benzoyloxydihydroagarofuran 

Relevant academic research and scientific papers

STEREOSELECTIVE TOTAL SYNTHESIS OF (+/-)-ISOCELORBICOL

A completely stereoselective total synthesis of the naturally occuring polyhydroxyagarofuran, (+/-)-isocelorbicol (1) is described.The readily available α-agarofuran derivative 3 was converted to 3β-hydroxy-9-keto-β-agarofuran (6) by epoxidation followed

Stereoselective Total Synthesis of (+/-)-Isocelorbicol

The naturally occurring trihydroxyagarofuran (+/-)-isocelorbicol (1) has been synthesized in 15 steps (3.2percent) from 9-keto-α-agarofuran (2).This completely stereoselective synthesis includes an osmium tetraoxide oxidation in which the reagent attacks