127627-96-7

Upstream product

• 104791-93-7 (+)-(1R,5R,7R)-7-mesyloxymethyl-6,8-dioxabicyclo<3.2.1>octane 
• 100-51-6 benzyl alcohol 
• 89927-11-7 Methanesulfonic acid (1R,3S,5R,7R)-3-(toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-ylmethyl ester 

Downstream Products

• 495-20-5 (+)-conhydrine 
• 127627-99-0 (R)-2-Benzyloxy-6-((R)-1-benzyloxy-propyl)-tetrahydro-pyran 
• 127628-01-7 (5R,6R)-6-Benzyloxy-5-hydroxy-octanoic acid methyl ester 
• 127628-00-6 (R)-6-((R)-1-Benzyloxy-propyl)-tetrahydro-pyran-2-one 
• 127628-02-8 (S)-6-((R)-1-Benzyloxy-propyl)-piperidin-2-one 
• 127627-98-9 (R)-1-((R)-6-Benzyloxy-tetrahydro-pyran-2-yl)-propan-1-ol 
• 127628-03-9 O-benzylconhydrine 
• 127627-97-8 (R)-2-Benzyloxy-6-(R)-oxiranyl-tetrahydro-pyran 

Relevant academic research and scientific papers

Enantiospecific synthesis of optically active natural (+)-conhydrine from (S,S)-tartaric acid

The first enantiospecific synthesis of (+)-conhydrine, one of the poisonous alkaloids of the hemlock was achieved via partial ring opening of 6,8-dioxabicyclo[3.2.1]-octane skeleton prepared from (S,S)-tartaric acid