1394245-86-3

Upstream product

• 6386-26-1 O¹,O²-isopropylidene-O⁵-benzyl-α-D-glucofuranose 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 5111-13-7 (1S,3R,4R,5S,8S)-8-benzyloxy-7-keto-3,4-isopropylidenedioxy-2,6-dioxabicyclo[3.3.0]octane 
• 142719-12-8 C₂₂H₃₆O₆Si 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 1394245-90-9 C₃₉H₇₂O₉Si₄ 
• 864512-90-3 trans-caffeoyl-6-O-D-glucono-γ-lactone 
• 1394245-97-6 C₂₅H₃₂O₇ 
• 1394245-92-1 C₂₀H₂₂O₆ 
• 1394245-94-3 C₃₉H₇₂O₉Si₄ 
• 1394245-99-8 (5S)-epi-vittarilide A 
• 1394245-87-4 C₂₅H₃₂O₇ 
• 1394245-89-6 C₂₀H₂₂O₆ 
• 94686-95-0 5,6-Di-O-benzyl-D-glucofuranose 

Relevant academic research and scientific papers

First total synthesis and absolute stereochemical assignment of vittarilide-A, an antioxidant extractive component isolated from Vittaria anguste-elongata Hayata

The first stereocontrolled synthesis of vittarilide-A and its C5-epimer was completed from d-glucuronolactone. Comparison with the spectroscopic properties reported for authentic material has given a clear indication as to the absolute stereochemistry of the natural vittarilide-A.