141858-95-9

Upstream product

• 3587-60-8 Benzyloxymethyl chloride 
• 141858-87-9 (4S,5R,E)-5-[(tert-butyldimethylsilyl)oxy]-4-methylhept-2-en-1-ol 
• 111149-36-1 (2S,3S,4RS,5RS)-5-benzyloxymethyl-4-bromo-2-ethynyl-3-methyltetrahydrofuran 
• 111149-37-2 (2R,3S,4RS,5RS)-5-benzyloxymethyl-4-bromo-2-ethyl-3-methyltetrahydrofuran 
• 141858-86-8 (4S,5R)-(E)-1-benzyloxy-5-tert-butyldimethylsilyloxy-4-methyl-2-heptene 
• 111149-40-7 (3R,4S)-(E)-7-benzyloxy-4-methylhept-5-en-3-ol 
• 110339-29-2 (R)-(Z)-1-Benzyloxy-2-hydroxy-3-pentene 
• 120448-41-1 (3R,4S)-(E)-7-benzyloxy-4-methylhept-5-en-1-yn-3-ol 
• 123372-87-2 (3S,4S)-(E)-7-benzyloxy-4-methylhept-5-en-1-yn-3-ol 
• 141207-20-7 Benzoic acid (E)-(1S,2S)-5-benzyloxy-1-ethynyl-2-methyl-pent-3-enyl ester 
• 111149-31-6 (3R,4S)-(E)-7-benzyloxy-4-methyl-1-trimethylsilylhept-5-en-1-yn-3-ol 
• 120448-40-0 (R)-(Z)-1-benzyloxy-2-propargyloxy-3-pentene 
• 111149-29-2 (R)-(Z)-1-benzyloxy-2-(3'-trimethylsilylpropargyloxy)-3-pentene 

Downstream Products

• 103563-54-8 (3R,4S)-(E)-7-<(benzyloxy)methoxy>-4-methyl-5-hepten-3-ol 

Relevant academic research and scientific papers

AN ENANTIOCONTROLLED ROUTE TO PROTOMYCINOLIDE IV AND ITS PRESUMED BIOGENETIC PRECURSORS USING (S)-O-BENZYLGLYCIDOL

Starting with (S)-O-benzylglycidol (9) as only chiral building block, a formal synthesis of protomycinolide IV (1) and the first syntheses of its presumed biogenetic precursors methyl epimycinonate I (2), methyl mycinonate I (3), methyl mycinonate II (4),