934808-43-2

Upstream product

• 69739-34-0 t-butyldimethylsiyl triflate 
• 748154-79-2 (2S,3S,5S,6S)-2-Iodomethyl-6-methoxy-5-(4-methoxy-benzyloxy)-tetrahydro-pyran-3-ol 

Downstream Products

• 863997-73-3 6-(4-methoxy-benzyloxy)-7,7a-dihydro-6H-benzofuran-2-one 
• 748154-83-8 (diethoxy-phosphoryl)-acetic acid 5-(4-methoxy-benzyloxy)-2-oxo-cyclohex-3-enyl ester 
• 863997-70-0 2-(tert-butyl-dimethyl-silanyloxy)-5-hydroxy-4-(4-methoxy-benzyloxy)-cyclohexanone 
• 863997-71-1 6-(tert-butyl-dimethyl-silanyloxy)-4-(4-methoxy-benzyloxy)-cyclohex-2-enone 
• 863997-72-2 6-hydroxy-4-(4-methoxy-benzyloxy)-cyclohex-2-enone 
• 863997-69-7 tert-butyl-[6-methoxy-5-(4-methoxy-benzyloxy)-2-methylene-tetrahydro-pyran-3-yloxy]-dimethyl-silane 

Relevant academic research and scientific papers

Direct observation of a target cell of the leaf-closing factor by using novel fluorescence-labeled phyllanthurinolactone

We report the synthesis of the fluorescence-labeled probe 2 based on phyllanthurinolactone 1, which is a leaf-closing substance of Phyllanthus urinaria L. Bioorganic studies using probe 2 showed leaf-closing activity at 1 × 10-5 M, which was on

Fluorescence study on the nyctinasty of Phyllanthus urinaria L. using novel fluorescence-labeled probe compounds

We report the synthesis of fluorescence-labeled probes based on phyllanthurinolactone 1, which is a leaf-closing substance of Phyllanthus urinaria L. The fluorescence study using biologically active probe 2 and inactive probes (epi-2 and 31) revealed that