83198-63-4

Upstream product

• 528-63-2 galgravin 
• 10569-12-7 (-)-Galbelgin 
• 88497-87-4 manassantin A 
• 1536263-71-4 (7R,7′S,8R,8′R)-4,4′-dibenzyloxy-3,3′-dimethoxy-7,7′-epoxylignane-9,9′-diol 
• 528-63-2 veraguensin 
• 1536264-02-4 C₃₆H₄₀O₁₁S₂ 
• 1536263-72-5 (7R,7′R,8S,8′S)-4,4′-dibenzyloxy-3,3′-dimethoxy-7,7′-epoxylignane-9,9′-diol 
• 1536263-75-8 (7S,7′S,8R,8′R)-4,4′-dibenzyloxy-3,3′-dimethoxy-7,7′-epoxylignane-9,9′-diol 
• 1536263-89-4 (7R,7′S,8S,8′R)-4,4′-dibenzyloxy-3,3′-dimethoxy-7,7′-epoxylignane-9,9′-diol 

Downstream Products

• 91377-15-0 malabaricanol diacetate 
• 5701-82-6 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylbutane 
• 3569-00-4 (+/-)-trans-4-(3,4-dimethoxyphenyl)-3,4-dihydro-6,7-dimethoxy-2,3-dimethylnaphthalene 
• 528-63-2 veraguensin 
• 528-63-2 galgravin 
• 528-63-2 galbelgin 
• 10569-12-7 (-)-Galbelgin 

Relevant academic research and scientific papers

Synthesis of all stereoisomers of 3,3-Dimethoxy-7,7-epoxylignane-4,4-diol and their plant growth inhibitory activity

All stereoisomers of 3,3-dimethoxy-7,7-epoxylignane-4,4-diol were synthesized to examine the effect of stereochemistry on their plant growth inhibitory activity using lettuce and Italian ryegrass. The effect of structural modifications such as dehydroxyla

Synthesis of all stereoisomers of 3,3′-dimethoxy-7,7′- epoxylignane-4,4′-diol and their plant growth inhibitory activity

All stereoisomers of 3,3′-dimethoxy-7,7′-epoxylignane-4, 4′-diol were synthesized to examine the effect of stereochemistry on their plant growth inhibitory activity using lettuce and Italian ryegrass. The effect of structural modifications such as dehydro

Glycosides from the bark of Machilus robusta

Six new glycosidic constituents (1-6), together with 10 known analogs, have been isolated from the bark of Machilus robusta. Structures of the new compounds, including the absolute configurations, were determined by spectroscopic and chemical methods as (

O-demethylation of 7,7'-epoxylignans by Aspergillus niger

Biotransformation of the 7,7'-epoxylignans, (+)-veraguensin, (+)- galbelgin and galgravin by Aspergillus niger has been investigated. These lignans were converted to their corresponding 4,4'-O-demethyl derivatives, (+)-verrucosin, (+)-fragransin A2/

MANASSANTINS A/B AND SAUCERNEOL: NOVEL BIOLOGICALLY ACTIVE LIGNOIDS FROM SAURURUS CERNUUS

From the extract of Saururus cernuus two toxic principles, manassantins A and B and a related substance, saucerneol, were isolated.They have novel dineolignan or sesquineolignan type structures.Although toxic, manassantin A showed potential neuroleptic activity.