873876-95-0

Upstream product

• 108-98-5 thiophenol 
• 873876-88-1 (E)-(5S,7R)-5,7-Dihydroxy-oct-2-enoic acid methyl ester 
• 300-87-8 3,5-dimethyl-1,2-oxazole 
• 873876-94-9 (1R,3R,5R)-1-Pyrrol-1-yl-hexane-1,3,5-triol 
• 873876-93-8 (Z)-(R)-5-Amino-1-hydroxy-1-pyrrol-1-yl-hex-4-en-3-one 
• 1026583-98-1 (R)-6-Hydroxy-6-pyrrol-1-yl-hexane-2,4-dione 
• 873876-92-7 (R)-2-(3-Methyl-isoxazol-5-yl)-1-pyrrol-1-yl-ethanol 
• 873876-90-5 2-(3-methyl-isoxazol-5-yl)-1-pyrrol-1-yl-ethanone 

Downstream Products

• 873876-96-1 3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionic acid (R)-1-methyl-2-((R)-6-oxo-4-phenylsulfanyl-tetrahydro-pyran-2-yl)-ethyl ester 
• 131613-66-6 (-)-<5(S),7(R)>-7-<5-(oct-2-enolide)-3',4'-bis-(t-butyldimethylsilyloxy)>-dihydrocinnamate 
• 71939-67-8 (R)-1-methyl-2-[(S)-6-oxo-3,6-dihydro-2H-pyran-2-yl]ethyl 3-(3,4-dihydroxyphenyl)propanoate 

Relevant academic research and scientific papers

A total synthesis of tarchonanthuslactone exploiting N-pyrrole carbinols as efficient stereocontrolling elements

(Chemical Equation Presented) A short stereoselective total synthesis of the polyketide natural product, tarchonanthuslactone, has been achieved. The key sequence involves the first reported catalytic enantioselective reduction of an N-acyl pyrrole and su