202798-30-9

Upstream product

• 149820-68-8 1,2-O-isopropylidene-D-chiro-inositol 
• 202798-29-6 3,4,5,6-tetra-O-benzyl-D-chiro-inositol 
• 628312-96-9 1,2-O-isopropylidene-3,4,5,6-tetra-O-benzyl-D-chiro-inositol 

Downstream Products

• 260447-16-3 1-D-6-O-allyl-2,3,4,5-tetra-O-benzyl-myo-inositol 
• 142436-07-5 2,3,4,5-O-Tetrabenzyl-D-myo-inositol 
• 132437-54-8 1-O-allyl-2,3,4,5-tetra-O-benzyl-D-myo-inositol 
• 202845-39-4 Acetic acid (1S,2R,3R,4S,5R,6R)-2,3,4,5-tetrakis-benzyloxy-6-hydroxy-cyclohexyl ester 

Relevant academic research and scientific papers

Ready routes to key myo-inositol component of GPIs employing microbial arene oxidation or Ferrier reaction

Microbial arene oxidation or Ferrier reaction of enol acetates provides versatile complementary routes that greatly facilitate preparation of inositol synthon(s) for GPI assembly.