351884-95-2

Downstream Products

• 351884-99-6 (1S,2S,3R,4S,5S,7R)-7-Benzyloxymethyl-2,3,4-tris-methoxymethoxy-6,8-dioxa-bicyclo[3.2.1]octane 
• 351884-97-4 Benzoic acid (1S,2S,4S,5S,6S,7R)-7-benzyloxymethyl-3,8,9-trioxa-tricyclo[4.2.1.0^2,4]non-5-yl ester 
• 351884-98-5 (1R,2S,3R,4S,5S,7R)-7-Benzyloxymethyl-6,8-dioxa-bicyclo[3.2.1]octane-2,3,4-triol 
• 184886-36-0 (1S,4R,5S,6R)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 
• 146830-44-6 (4R,5S,6S)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enone 
• 146830-45-7 (1R,4R,5S,6R)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 
• 123238-09-5 (1R,2R,3S,4R)-cyclohex-5-ene-1,2,3,4-tetrol 
• 526-87-4 conduritol A 
• 351884-96-3 (1S,2S,4S,5S,6R,7R)-7-Benzyloxymethyl-3,8,9-trioxa-tricyclo[4.2.1.0^2,4]nonan-5-ol 

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.