99623-84-4

Upstream product

• 61227-22-3 methyl 2-hydroxy-5-(phenylmethoxy)benzoate 
• 142592-60-7 <2S(S),3R,6S,8S>-N-<6-hydroxy-2-(methoxycarbonyl)-3-<<2-(trimethylsilyl)ethoxy>methoxy>phenyl>-2-<1-<<1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-pyrrolidyl>carbonyl>ethyl>-1,7-dioxaspiro<5.5>undecane-8-acetamide 
• 142592-61-8 <2<2S(S),3R,6S,8S>> methyl 5-hydroxy-2-<3-methyl-2-<1-<<1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-pyrrolidyl>carbonyl>ethyl>-1,7-dioxaspiro<5.5>undecan-8-yl>-4-benzoxazolecarboxylate 
• 142592-58-3 <2S(2S,3R,6S,8S)>-2-<3-methyl-8-<2-(benzyloxy)ethyl>-1,7-dioxaspiro<5.5>undecan-2-yl>-1-<1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-pyrrolidyl>-1-propanone 
• 142592-76-5 (βR,2S,3R,6S,8S)-2-<α-(tert-butyldiphenylsilyloxy)ethyl>-8-<2-(benzyloxy)ethyl>-β,3-dimethyl-1,7-dioxaspiro<5.5>undecane 
• 142592-59-4 <2S(S),3R,6S,8S>-3-methyl-2-<1-<<1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-pyrrolidyl>carbonyl>ethyl>-1,7-dioxaspiro<5.5>undecane-8-acetic acid 
• 144604-71-7 (βR,2S,3R,6S,8S)-2-[α-(tert-butyldiphenylsilyloxy)ethyl]-β,3-dimethyl-1,7-dioxaspiro[5.5]undecane-8-ethanol 
• 144604-78-4 (S)-2-[(2S,3R,6S,8S)-8-(2-Hydroxy-ethyl)-3-methyl-1,7-dioxa-spiro[5.5]undec-2-yl]-1-[1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrol-2-yl]-propan-1-one 
• 142592-55-0 methyl 5-oxo-6-<(phenylselenyl)imino>-2-<<2-(trimethylsilyl)ethoxy>methoxy>-1,3-cyclohexadienecarboxylate 
• 142592-52-7 5-Benzyloxy-2-(2-trimethylsilanyl-ethoxymethoxy)-benzoic acid methyl ester 
• 142592-41-4 (2RS,6S)-6-<2-(benzyloxy)ethyl>tetrahydro-2-(phenylsulphonyl)-2H-pyran 
• 142592-57-2 (αR,2S,3R,6S,8S)-8-<2-(benzyloxy)ethyl>-α,3-dimethyl-1,7-dioxaspiro<5.5>undecane-2-ethanal 
• 142592-56-1 (βR,2S,3R,6S,8S)-8-<2-(benzyloxy)ethyl>-β,3-dimethyl-1,7-dioxaspiro<5.5>undecane-2-ethanol 
• 142592-43-6 methyl 2-amino-3-hydroxy-6-<<2-(trimethylsilyl)ethoxy>methoxy> benzoate 

Relevant academic research and scientific papers

Eight-step synthesis of routiennocin

Routiennocin is a member of a family of polycyclic pyrrole ether antibiotics that simultaneously uncouple oxidative phosphorylation and inhibit ATPase as a result of selective complexation of divalent metal ions. We describe a concise synthesis of routien

Total synthesis of the ionophore antibiotic CP-61,405 (routiennocin)

The total synthesis of the spiroketal ionophore antibiotic routiennocin 1 (CP-61,405) employing π-allyltricarbonyl iron lactone complexes is described. These complexes were used as precursors for the preparation of substituted 2-phenylsulphonyl pyrans whi