852327-49-2

Upstream product

• 13154-24-0 triisopropylsilyl chloride 
• 258263-05-7 triisopropyl-(2-oxiranyl-ethoxy)-silane 
• 852327-44-7 trifluoro-methanesulfonic acid 7-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-2,2-dimethyl-4-oxo-4H-benzo[1,3]dioxin-5-yl ester 
• 852327-36-7 1-Methoxy-4-[(S)-1-(2-triisopropylsilanyloxy-ethyl)-4-trimethylsilanyl-but-3-ynyloxymethyl]-benzene 
• 852327-51-6 [(E)-(S)-6-Iodo-3-(4-methoxy-benzyloxy)-hex-5-enyloxy]-triisopropyl-silane 
• 852327-43-6 7-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-hydroxy-2,2-dimethyl-benzo[1,3]dioxin-4-one 
• 852327-50-5 ((S)-3-(4-methoxybenzyloxy)hex-5-ynyloxy)triisopropylsilane 
• 852327-35-6 (S)-1-Triisopropylsilanyloxy-6-trimethylsilanyl-hex-5-yn-3-ol 
• 852327-46-9 7-(2-hydroxy-ethoxy)-2,2-dimethyl-5-(3-methyl-but-2-enyl)-benzo[1,3]dioxin-4-one 
• 852327-33-4 6-iodo-1-triisopropylsilanyloxy-hex-5-en-3-ol 
• 852327-34-5 Triisopropyl-((R)-2-oxiranyl-ethoxy)-silane 
• 438187-00-9 4-(methoxyimino)-(2E)-butenamide 
• 169310-77-4 1-triisopropylsiloxy-3-butene 
• 137571-73-4 5,7-dihydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one 

Downstream Products

• 1027170-53-1 4-{2-[3-(4-Benzoyl-phenyl)-propionylamino]-ethoxy}-2-hydroxy-6-(3-methyl-but-2-enyl)-benzoic acid (E)-(S)-4-((E)-4-methoxyimino-but-2-enoylamino)-1-(2-triisopropylsilanyloxy-ethyl)-but-3-enyl ester 

Relevant academic research and scientific papers

Synthesis of photoactivatable acyclic analogues of the lobatamides

(Chemical Equation Presented) The lobatamides and related salicylate enamide natural products are potent mammalian V-ATPase inhibitors. To probe details of binding of the lobatamides to mammalian V-ATPase, three photoactivatable analogues bearing benzophe