82299-37-4

Upstream product

• 302968-94-1 2-(benzo-1,3-dioxol-5-yl)-1,3-dimethylimidazolidine 
• 7797-83-3 2H-benzo[d]1,3-dioxolane-4-carbaldehyde 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 82299-36-3 bromo-5 hydroxy-4 benzodioxole-1,3 
• 24677-78-9 2,3-dihydroxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 69393-72-2 2H-benzo[d][1,3]dioxolan-4-ol 
• 120-57-0 piperonal 
• 23780-59-8 4-hydroxybenzo[d][1,3]dioxole-5-carbaldehyde 
• 93-61-8 N-methyl-N-phenylformamide 
• 115943-52-7 4-(phenylmethoxy)-1,3-benzodioxole 
• 100-44-7 benzyl chloride 

Downstream Products

• 82299-38-5 acide (benzyloxy-2 methylenedioxy-3,4 phenyl)-4 methoxycarbonyl-3 butene-3 oique 
• 1025823-93-1 6-Benzoyl-5-[(4-benzyloxy-benzo[1,3]dioxol-5-yl)-hydroxy-methyl]-5,6-dihydro-[1,3]dioxolo[4,5-g]isoquinoline-5-carbonitrile 
• 180728-47-6 (4-Benzyloxy-benzo[1,3]dioxol-5-yl)-[1,3]dioxolo[4,5-g]isoquinolin-5-yl-methanone 
• 180728-46-5 (4-Benzyloxy-benzo[1,3]dioxol-5-yl)-[1,3]dioxolo[4,5-g]isoquinolin-5-yl-methanol 
• 82314-35-0 (5aS,8aR)-10-Benzyloxy-5-hydroxy-5-(3,4,5-trimethoxy-phenyl)-5,8,8a,9-tetrahydro-5aH-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6-one 
• 82299-45-4 (5aR,8aR)-10-Benzyloxy-5-(3,4,5-trimethoxy-phenyl)-5,8,8a,9-tetrahydro-5aH-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6-one 
• 477-50-9 (+/-)-iso β-peltatine 
• 92830-78-9 (benzyloxy-2 methylenedioxy-3,4 benzyl)-4 <(trimethoxy-3,4,5-phenyl)hydroxymethyl>-3 dihydro-3H-furannone-2 
• 82299-45-4 O-benzyl (+/-)-iso-β-peltatine 
• 477-50-9 (+/-)-iso-β-peltatine 
• 82299-39-6 (benzyloxy-2 methylenedioxy-3,4 benzylidene)-4 dihydro-3H-furannone-2 
• 82299-41-0 (benzyloxy-2 methylenedioxy-3,4 benzyl)-4 dihydro-3H-furannone-2 
• 302969-13-7 [2-(4-benzyloxy-benzo[1,3]dioxol-5-ylmethyl)-piperidin-1-yl]-(4-benzyloxy-3,5-dimethoxy-phenyl)-methanone 
• 302969-11-5 2-[1-(4-Benzyloxy-benzo[1,3]dioxol-5-yl)-meth-(E)-ylidene]-piperidine-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

First synthesis and pharmacological evaluation of benzoindolizidine and benzoquinolizidine analogues of α- and β-peltatin

The benzoindolizidine and-quinolizidine analogues of α- and β-peltatin were designed and synthesized by two different synthetic routes involving as the key step the Bischler-Napieralski cyclization of suitably substituted N-acyl-2-arylmethylpyrrolidine and -piperidine derivatives. The in vitro biological activity of these analogues as well as some of their derivatives was subsequently evaluated. Copyright (C) 2000 Elsevier Science Ltd.

Topical Nonsteroidal Antipsoriatic Agents. 2. 2,3-(Alkylidenedioxy)naphthalene Analogues of Lonapalene

A series of 2,3-(alkylidenedioxy)naphthalene analogues (5a-p) of lonapalene (RS-43179,1), a 5-lipoxygenase inhibitor currently under clinical investigation for the treatment of psoriasis, has been prepared and evaluated for topical inhibitory activity aga

SYNTHESE TOTALES DE LA (+/-) ISO β-PELTATINE ET DE SES ANALOGUES

α-Hydroxyalkylation of a β-(2-alkoxy 3,4-methylenedioxy benzyl)-γ-butyrolactone (17 or 25) with 3,4,5-trimethoxybenzaldehyde or syringaldehyde 27, followed by cyclisation, afforded good yields of the corresponding (+/-) isopeltatins.