22882-57-1

Upstream product

• 2065-66-9 methyl-triphenylphosphonium iodide 
• 1309586-76-2 ent-10β,13-dihydroxy-2α,3α-epoxy-16-oxo-17,20-dinorgibberellane-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 1309586-75-1 ent-10β,13-dihydroxy-2α,3α-epoxy-16-oxo-17,20-dinorgibberellane-7,19-dioic acid 7-methoxymethyl ester 19,10-lactone 
• 1309586-72-8 ent-13-acetoxy-2α,3α-epoxy-10β-hydroxy-16-oxo-17,20-dinorgibberellane-7,19-dioic acid 7-methoxymethyl ester 19,10-lactone 
• 1309586-73-9 C₂₂H₂₆O₈ 
• 67-56-1 methanol 
• 81010-90-4 C₂₉H₃₅BrO₈Si 
• 22883-04-1 C₂₃H₃₂O₆Si 

Downstream Products

• 1309586-78-4 ent-3α,13-bis-tetrahydropyran-2-yloxy-10β-hydroxy-2β-phenylmethoxy-20-norgibberell-16-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 1309586-79-5 ent-2β-phenylmethoxy-3α,10β,13-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 19,10-lactone 
• 1309586-82-0 ent-3α,13-bis-tetrahydropyranyloxy-10β-hydroxy-2β-phenethyloxy-20-norgibberell-16-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 1309586-84-2 ent-2β-phenethyloxy-3α,10β,13-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 19,10-lactone 
• 1309586-88-6 ent-10β,13-dihydroxy-2β-(3-phenylpropanoxy)-3α-tetrahydropyran-2-yloxy-20-norgibberell-16-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 1309586-87-5 ent-3α,13-bis-tetrahydropyran-2-yloxy-10β-hydroxy-2β-(3-phenylpropanoxy)-20-norgibberell-16-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 1309586-89-7 ent-2β-(3-phenylpropanoxy)-3α,10β,13-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 19,10-lactone 
• 1309586-86-4 ent-2β-(3-phenylpropanoxy)-3α,10β,13-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 1309586-80-8 ent-2β-phenethyloxy-3α,10β,13-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 
• 1309586-77-3 ent-2β-phenylmethoxy-3α,10β,13-trihydroxy-20-norgibberell-16-ene-7,19-dioic acid 7-methyl ester 19,10-lactone 

Relevant academic research and scientific papers

Studies directed towards the preparation of probes for the photoaffinity labelling of gibberellin receptors

Model studies for the preparation of photoaffinity probes designed to explore the nature of gibberellin receptor sites have provided a wide range of gibberellin derivatives that should afford useful scaffolds incorporating auxiliary groups attached to C-2

CHLOROETHOXY(TRIMETHYL)SILANE : A HARD-BASE TRAP WHICH PRESERVES TMS ETHER GROUPS AND IMPROVES THE WITTIG METHYLENATION OF GIBBERELLINS

A reagent, 2-chloroethoxy(trimethyl)silane (CETS), has been devised which ensures the preservation of TMS ether groups during Wittig methylenation in protic media and which makes this formerly capricious reaction with 16-keto gibberellins a reliable and straightforward procedure.