75759-30-7

Upstream product

• 98-88-4 benzoyl chloride 
• 510-50-9 gibberellic acid methyl ester 
• 75759-23-8 C₂₁H₂₈O₉ 
• 75759-25-0 C₂₁H₂₆O₇ 
• 75759-26-1 C₂₁H₂₆O₇ 
• 79936-49-5 C₂₇H₃₂O₁₀S 
• 75759-22-7 C₂₇H₃₂O₁₀S 
• 75759-22-7 C₂₇H₃₂O₁₀S 
• 75759-24-9 C₂₈H₃₁BrO₉ 
• 75759-28-3 C₂₈H₃₀O₉ 
• 75759-29-4 C₂₆H₂₆O₈ 
• 75758-88-2 (+/-)-(1α,2α,4aα,4bβ,10β)-8,8-(Ethylenedioxy)-2,7-dihydroxy-10-(methoxycarbonyl)-1-methylgibbane-1,4a-carbolactone 
• 75759-27-2 C₃₀H₃₅NO₈ 
• 80994-37-2 C₂₉H₃₄O₈Si 

Downstream Products

• 79936-42-8 ent-13-acetoxy-3α-benzoyloxy-10β-hydroxy-20-norgibberella-1,16-diene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 75759-29-4 ent-3α-benzoyloxy-10β,13-hydroxy-16-oxo-17,20-dinorgibberell-1-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 79936-43-9 ent-13-acetoxy-3α-benzoyloxy-10β-hydroxy-16-oxo-17,20-dinorgibberell-1-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 75759-22-7 ent-16,16-ethylenedioxy-10β,13-dihydroxy-3α-phenylsulfonyloxy-17,20-dinorgibberellane-17,19-dioic acid 7-methyl ester 19,10-lactone 
• 510-50-9 gibberellic acid methyl ester 

Relevant academic research and scientific papers

Improved Procedures for the Degradation of Gibberellic acid. The Preparation of Substrates for Synthetic Studies

Gibberellic acid has been efficiently degraded to methyl 16-oxo-17-norgibberellate (8), to 16-oxo-17-norgibberellin A1 methyl ester (9), and to (15), the 3α-epimer of (9).Both (9) and (15) were protected as their acetal derivatives (10) and (16) respectiv