243987-96-4

Downstream Products

• 351885-00-2 4-Nitro-benzoic acid (1R,2R,5S,7R)-7-benzyloxymethyl-6,8-dioxa-bicyclo[3.2.1]oct-3-en-2-yl ester 
• 1283695-54-4 (1R,4S,5R,7R)-7-(benzyloxymethyl)-6,8-dioxabicyclo[3.2.1]oct-2-en-4-yloxy tert-butyldimethylsilane 
• 1283695-41-9 (1R,4S,5R,7R)-7-(benzyloxymethyl)-6,8-dioxabicyclo[3.2.1]oct-2-en-4-ol 
• 1283695-39-5 (1S,2R,5S,7R)-7-(benzyloxymethyl)-2-phenylthio-6,8-dioxabicyclo[3.2.1]oct-3-ene 
• 351885-01-3 4-Nitro-benzoic acid (1S,2R,3R,4S,5S,7R)-7-benzyloxymethyl-3,4-dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester 
• 351884-94-1 (1S,2S,3S,4S,5S,7R)-7-Benzyloxymethyl-2,3,4-tris-methoxymethoxy-6,8-dioxa-bicyclo[3.2.1]octane 
• 351885-02-4 (1S,2R,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 
• 351885-23-9 (1S,4R,5R,6S)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 
• 351885-27-3 4-Nitro-benzoic acid (1R,4R,5R,6R)-4,5,6-tris-methoxymethoxy-cyclohex-2-enyl ester 
• 351885-24-0 (1S,4S,5R,6R)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 
• 266693-94-1 (1S,4R,5R,6R)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 
• 351885-28-4 (1R,4R,5R,6R)-4,5,6-Tris-methoxymethoxy-cyclohex-2-enol 
• 4782-75-6 conduritol D 

Relevant academic research and scientific papers

Total synthesis of aspergillide A and B based on the transannular oxy-Michael reaction

Keys to the kingdom: A highly efficient and diastereoselective transannular oxy-Michael reaction for the construction of the syn- and anti-tetrahydropyran units from a common 14-membered macrolactone is the key step for the total synthesis of aspergillide

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.