351885-27-3

Upstream product

• 266693-94-1 (1S,4R,5R,6R)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 
• 62-23-7 4-nitro-benzoic acid 
• 266693-87-2 C₁₈H₁₉BrO₅ 
• 266693-92-9 C₁₇H₂₇BrO₇ 
• 266693-93-0 (1S,4R,4aS,5S,6R,7R,8R,8aR)-6,7,8-Tris-methoxymethoxy-1,4,4a,5,6,7,8,8a-octahydro-1,4-methano-naphthalen-5-ol 
• 173201-10-0 C₁₁H₁₃BrO₂ 
• 146830-39-9 C₁₃H₁₇BrO₃ 
• 351884-94-1 (1S,2S,3S,4S,5S,7R)-7-Benzyloxymethyl-2,3,4-tris-methoxymethoxy-6,8-dioxa-bicyclo[3.2.1]octane 
• 351884-93-0 (1S,2S,3R,4S,5S,7R)-7-Benzyloxymethyl-2-methoxymethoxy-6,8-dioxa-bicyclo[3.2.1]octane-3,4-diol 
• 351885-06-8 (1R,2S,3S,4S,5R,7S)-7-Iodomethyl-2,3,4-tris-methoxymethoxy-6,8-dioxa-bicyclo[3.2.1]octane 
• 351885-03-5 ((1S,2S,3S,4S,5S,7R)-2,3,4-Tris-methoxymethoxy-6,8-dioxa-bicyclo[3.2.1]oct-7-yl)-methanol 
• 351885-15-9 (3S,4R,5R,6R)-4,5,6-Tris-methoxymethoxy-oct-1-en-7-yn-3-ol 
• 351885-19-3 (3S,4R,5R,6R)-4,5,6-Tris-methoxymethoxy-octa-1,7-dien-3-ol 
• 351884-92-9 (1R,2S,5S,7R)-7-Benzyloxymethyl-2-methoxymethoxy-6,8-dioxa-bicyclo[3.2.1]oct-3-ene 

Downstream Products

• 137567-79-4 (1R,2R,3R,4R)-5-cyclohexene-1,2,3,4-tetrol 
• 351885-28-4 (1R,4R,5R,6R)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 

Relevant academic research and scientific papers

A New Convergent Route to Conduritols A-F from a Common Chiral Building Block

(matrix presented) A diastereocontrolled route to conduritols A-F has been developed starting from a common chiral building block containing an oxabicyclo-[3.2.1]octane framework.

Integrated synthesis of conduritols A-F using a single chiral building block

Six possible diastereomers of conduritols have been synthesized diastereoselectively in an integrated manner starting from a single chiral precursor, which served as a synthetic equivalent of chiral cis-1,4-dihydroxycyclohexa-2,5-diene.