780820-87-3

Upstream product

• 185617-14-5 (R)-homotyrosine hydrobromide 
• 477289-51-3 (D)-(-)-methyl homotyrosinate 
• 780820-85-1 3-(tert-butyl-diphenyl-silanyloxymethyl)-octahydro-4-thia-3a-aza-cyclopenta[c]indene 4,4-dioxide 
• 2984-50-1 1,2-Epoxyoctane 
• 780820-77-1 (R)-2-Hydroxymethyl-1-methanesulfonyl-1-aza-spiro[4.5]deca-6,9-dien-8-one 
• 780820-79-3 2-(tert-butyl-diphenyl-silanyloxymethyl)-1-methanesulfonyl-1-aza-spiro[4.5]deca-6,9-dien-8-one 
• 780820-97-5 (D)-(+)-N,O-bis(methanesulfonyl)-methyl homotyrosinate 
• 780820-98-6 (D)-(+)-N,4'O-bis(methanesulfonyl)-homotyrosinol 
• 780820-76-0 (D)-(-)-N-methanesulfonyl-homotyrosinol 

Downstream Products

• 780820-93-1 (3R,5R,7aR,11aR)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-5-hexyl-octahydro-pyrrolo[2,1-j]quinolin-7-one 
• 780821-00-3 (3R,5S,7aR,11aR)-3-[[(tert-butyldiphenylsilyl)oxy]methyl]-5-hexyloctahydro-pyrrolo-1H-pyrrolo[2,1-j]quinolin-7(7aH)-one 
• 780820-96-4 (3R,5S,7S,7aS,11aR)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-5-hexyl-7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-decahydro-pyrrolo[2,1-j]quinoline 
• 780820-91-9 (S)-1-[(2R,5R,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-1-aza-spiro[4.5]dec-6-yl]-1-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-nonan-3-one 
• 780820-92-0 (3R,5R,7S,7aR,11aR)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-5-hexyl-decahydro-pyrrolo[2,1-j]quinolin-7-ol 
• 780820-99-7 (3R,5S,7aR,11aR)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-5-hexyl-decahydro-pyrrolo[2,1-j]quinolin-7-ol 

Relevant academic research and scientific papers

Synthetic ventures inspired by biosynthetic hypotheses: the evolution of a method for the oxidative amidation of phenols

We describe the development of a technique for the oxidative conversion of 4-alkyl phenols to derivatives of the corresponding 4-alkyl-4-amino-2,5-cyclohexanediones. This transformation, which was inspired by biogenetic considerations, constitutes a key s

Fully stereocontrolled total syntheses of (-)-cylindricine C and (-)-2-epicylindricine C: A departure in sulfonamide chemistry

A common intermediate was used in the total syntheses of (-)-cylindricine C and (-)-2-epicylindricine C (see picture) in a process that involves the initial oxidative spirocyclization of a phenolic sulfonamide. The remainder of the molecules is constructe