121330-23-2

Upstream product

• 121330-22-1 (1R,2R,3S,4S,1'S)-3-exo-(1'-hydroxy-2'(E)-octan-1'-yl)-7-oxabicyclo<2.2.1>hept-5-ene-2-exo-methanol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 61307-38-8 1-heptynylmagnesium bromide 
• 628-71-7 1-Heptyne 
• 68940-38-5 exo-4.7-Epoxy-1.3.3a.4.7.7a-hexahydroisobenzofuran-1-ol 
• 121421-29-2 (1R,2R,3R,4S,1'R)-3-exo-(1'-hydroxy-2'-octyn-1'-yl)-7-oxabicyclo<2.2.1>hept-5-ene-2-exo-methanol 

Downstream Products

• 121330-25-4 (1R,2R,3R,4S,3'S)-2-exo-<(tert-butyldiphenylsilyl)oxy>-3-exo-(3'-acetoxy-1'(E)-octen-1'-yl)-7-oxabicyclol<2.2.1>hept-5-ene 
• 121330-26-5 1-<(tert-butyldiphenylsilyl)oxy>-6(S)-acetoxy-2(Z),4(E)-undecadiene 
• 121330-24-3 (1R,2R,3S,4S,1'S)-2-exo-<(tert-butyldiphenylsilyl)oxy>-3-exo-(1'-acetoxy-2'(E)-octen-1'-yl)-7-oxabicyclol<2.2.1>hept-5-ene 

Relevant academic research and scientific papers

Efficient Synthesis of Sterically and Optically Pure E,Z Conjugated Hydroxy Dienes. A New Approach to Hydroxyeicosatetraenoic Acids

A new strategy for the synthesis of optically active E,Z conjugated hydroxy dienes, important intermediates for the synthesis of HETEs, is described.It involves as its key steps two successive chirality transfers starting from the tricyclic lactol 5, easi