875439-73-9

Upstream product

• 875439-71-7 3-[3-tert-butoxycarbonylamino-5-(tert-butyl-diphenyl-silanyloxy)-phenyl]-1-trimethylsilyl-propyne 
• 875439-72-8 3-[3-tert-butoxycarbonylamino-5-hydroxy-phenyl]-1-propyne 
• 75-24-1 trimethylaluminum 

Downstream Products

• 875439-60-4 N,O-bis(2-trimethylsilylethoxycarbonyl)-3-amino-5-[(E)-3-iodo-2-methylallyl]-phenol 
• 936824-96-3 N,O-bis(2-trimethylsilylethoxycarbonyl)-3-amino-5-(2-methyl-penta-2,4-dienyl)-phenol 
• 936824-92-9 3-(tert-butyl-diphenyl-silanyloxy)-5-(2-methyl-penta-2,4-dienyl)-phenylamine 
• 936824-93-0 C₅₃H₈₀O₆Si₃IN 
• 936824-95-2 C₅₅H₈₃O₆Si₃N 
• 875439-83-1 3,7-bis-(tert-butyl-dimethyl-silanyloxy)-10-methoxy-4,6,14-trimethyl-9-oxo-15-[3-(2-trimethylsilanyl-ethoxycarbonylamino)-5-(2-trimethylsilanyl-ethoxycarbonyloxy)-phenyl]-pentadeca-4,11,13-trienethioic acid S-(2-acetylamino-ethyl) ester 
• 875439-82-0 (4E,11E,13E)-(3S,6S,7S,10R)-3,7-Bis-(tert-butyl-dimethyl-silanyloxy)-10-methoxy-4,6,14-trimethyl-9-oxo-15-[3-(2-trimethylsilanyl-ethoxycarbonylamino)-5-(2-trimethylsilanyl-ethoxycarbonyloxy)-phenyl]-pentadeca-4,11,13-trienoic acid 
• 875439-68-2 Carbonic acid 3-[(2E,4E,11E)-(6R,7R,9S,10S,13S)-9,13-bis-(tert-butyl-dimethyl-silanyloxy)-7,15-dihydroxy-6-methoxy-2,10,12-trimethyl-pentadeca-2,4,11-trienyl]-5-(2-trimethylsilanyl-ethoxycarbonylamino)-phenyl ester 2-trimethylsilanyl-ethyl ester 
• 875439-81-9 Carbonic acid 3-[(2E,4E,11E)-(6R,9S,10S,13S)-9,13-bis-(tert-butyl-dimethyl-silanyloxy)-6-methoxy-2,10,12-trimethyl-7,15-dioxo-pentadeca-2,4,11-trienyl]-5-(2-trimethylsilanyl-ethoxycarbonylamino)-phenyl ester 2-trimethylsilanyl-ethyl ester 
• 875439-84-2 (4E,11E,13E)-(3S,6S,7S,10R)-3,7-Dihydroxy-10-methoxy-4,6,14-trimethyl-9-oxo-15-[3-(2-trimethylsilanyl-ethoxycarbonylamino)-5-(2-trimethylsilanyl-ethoxycarbonyloxy)-phenyl]-pentadeca-4,11,13-trienethioic acid S-(2-acetylamino-ethyl) ester 

Relevant academic research and scientific papers

Chemoenzymatic approaches toward dechloroansamitocin P-3

Equation Presented The enantioselective total synthesis of proansamitocin, a key biosynthetic intermediate of the highly potent antitumor agent ansamitocin P-3, is described which bears a diene-ene RCM as the key macrocyclization step. Feeding of proansam

Synthesis of the N-acetylcysteamine thioester of seco-proansamitocin

(Chemical Equation Presented) The enantioselective total synthesis of the N-acetylcysteamine thioester of seco-proansamitocin, a key biosynthetic intermediate of the highly potent antitumor agent ansamitocin, is described, which twice utilizes the Nagao a