101312-79-2

Usage

Uses

Used in Pharmaceutical Industry:
(1S,3aR)-1β,7-Dimethoxy-4β-(3-methoxy-4-hydroxyphenyl)-1,3,3aβ,4,9,9aα-hexahydronaphtho[2,3-c]furan-6-ol is used as a potential pharmaceutical candidate for its possible antioxidant or pharmacological properties. The presence of multiple methoxy and hydroxy groups, along with the naphthofuran ring system, may contribute to its biological activity, making it a promising compound for the development of new drugs.
Used in Organic Chemistry Research:
In the field of organic chemistry, (1S,3aR)-1β,7-Dimethoxy-4β-(3-methoxy-4-hydroxyphenyl)-1,3,3aβ,4,9,9aα-hexahydronaphtho[2,3-c]furan-6-ol serves as a subject of interest for researchers. Its complex structure and functional groups provide opportunities for studying synthesis methods, reactions, and potential applications in various organic chemical processes.
Note: The specific applications and uses of (1S,3aR)-1β,7-Dimethoxy-4β-(3-methoxy-4-hydroxyphenyl)-1,3,3aβ,4,9,9aα-hexahydronaphtho[2,3-c]furan-6-ol are not explicitly provided in the materials. The uses listed above are inferred based on the compound's structural features and potential for biological activity. Further research and experimentation would be required to confirm its actual applications and efficacy.

Upstream product

• 72724-00-6 1-(benzyloxy)-4-(bromomethyl)-2-methoxybenzene 
• 50766-69-3 2-(4-benzyloxy-3-methoxyphenyl)-1,3-dithiane 
• 89067-60-7 O-dibenzyl-β-conidendrine 
• 89067-60-7 (d,l)-O-dibenzyl α-conidendrine 
• 105783-67-3 O-dibenzyl-(+/-)-β-conidendral 
• 89067-57-2 (benzoxy-4 methoxy-3)benzyl-2(benzoxy-4 methoxy-3 α,α-propylenedithio)benzyl-3 butanolide 
• 89067-58-3 (+/-)-trans-2-(3-methoxy-4-benzyloxybenzyl)-3-(3'-metyhoxy-4'-benzyloxy-α-benzoyl)butyrolactone 
• 89067-59-4 O-dibenzylhydroxymatairesinol 
• 105783-66-2 (benzoxy-4 methoxy-3 α,α-propylene dithio)benzyl-3 butanolide 
• 105783-68-4 O-dibenzyl methyl-(+/-)-β-conidendral 
• 105783-67-3 O-dibenzyl epi-1-(+/-)-α-conidendral 
• 105783-68-4 O-dibenzyl methyl epi-1-(+/-)-α-conidendral 
• 71724-99-7 (1R,3aR,4S,9aR)-1,7-dimethoxy-4-(4'-hydroxy-3'-methoxyphenyl)-1,3,3a,4,9,9a-hexahydronaphtho<2,3-c>furan-6-ol 

Downstream Products

• 71724-99-7 (1R,3aR,4S,9aR)-1,7-dimethoxy-4-(4'-hydroxy-3'-methoxyphenyl)-1,3,3a,4,9,9a-hexahydronaphtho<2,3-c>furan-6-ol 
• 518-55-8 conidendrin 
• 71724-97-5 (1S,3aR,4S,9aR)-4-(4'-acetoxy-3'-methoxyphenyl)-1,7-dimethoxy-1,3,3a,4,9,9a-hexahydronaphtho<2,3-c>furan-6-yl acetate 
• 133694-85-6 (1S,3aR,4S,9aR)-4-(3,4-Dimethoxy-phenyl)-1,6,7-trimethoxy-1,3,3a,4,9,9a-hexahydro-naphtho[2,3-c]furan 
• 25047-22-7 (-)-O-Diacetyl-α-conidendrine 
• 133553-64-7 Acetic acid 4-(4-acetoxy-3-methoxy-phenyl)-7-methoxy-1-oxo-1,3-dihydro-naphtho[2,3-c]furan-6-yl ester 
• 71724-97-5 O-diacetyl methyl epi-1-(+/-)-α-conidendral 
• 5447-65-4 O-diacetyl-(+/-)-α-conidendrine 
• 71724-97-5 O-diacetyl methyl-(+/-)-β-conidendral 

Relevant academic research and scientific papers

ETUDES DE LIGNANES 7 - SYNTHESES TOTALES DES (+-)-α ET -β-CONIDENDRINES ET DES METHYL (+-)-α ET -β-CONIDENDRALS

Michael addition of the carbanion of the dithian 8 on butenolide, followed by alkylation with the benzylic bromide 11 and regeneration of the ketonic carbonyl group, gave the α,β-disubstituted lactone 13.Reduction of the ketonic carbonyl of the latter usi

Chemistry of the Podocarpaceae. LXIX. Further Lignans from the Wood of Dacrydium intermedium

Structures and absolute configurations are established for five new lignans isolated from the wood of the New Zealand podocarp Dacrydium intermedium Kirk.X-ray crystallography has been used to confirm the structure of one of the new lignans.Structures for two further inseparable lignans are provisionally assigned.The structure of one of three lignans previously isolated from the wood is revised.