132169-30-3

Upstream product

• 90407-20-8 2-bromo-3-(hydroxymethyl)-1-nitrobenzene 
• 573-54-6 2-bromo-3-nitro-benzoic acid 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 156263-59-1 2-bromo-3-(tert-butyldimethylsilyloxymethyl)-N-allylaniline 
• 132169-32-5 3-(N-acetyl-N-allylamino)-2-bromobenzaldehyde 
• 132169-31-4 3-(N-acetyl-N-allylamino)-2-bromobenzyl alcohol 
• 132169-33-6 3-(N-acetyl-N-allylamino)-2-bromophenyl acetaldehyde 
• 132169-38-1 N-2-<3-(N-acetyl-N-allylamino)-2-bromophenyl>ethenyl-2-(phenythiomethyl)prop-2-enylmethylamine 
• 151883-04-4 N-Allyl-N-[2-bromo-3-((E)-2-methylamino-vinyl)-phenyl]-acetamide 
• 156263-62-6 3-(N-benzoyl-N-allylamino)-2-bromobenzaldehyde 
• 156263-63-7 3-(N-trifluoroacetyl-N-allylamino)-2-bromobenzaldehyde 
• 156263-61-5 3-(N-trifluoroacetyl-N-allylamino)-2-bromobenzyl alcohol 
• 156263-67-1 N-1-<2-(3'-N-acetyl-N-allylamino)-2'-bromophenyl>ethenylpyrrolidine 
• 156263-60-4 3-(N-benzoyl-N-allylamino)-2-bromobenzyl alcohol 
• 156263-66-0 3-(N-trifluoroacetyl-N-allylamino)-2-bromophenyl acetaldehyde 
• 156263-73-9 N-2-<3-(N-acetyl-N-allylamino)-2-bromophenyl>ethenyl-2-(methoxycarbonyl)prop-2-enylmethylamine 
• 151883-03-3 3-<3-(N-acetyl-N-allylamino)-2-bromophenyl>-5-(methoxycarbonyl)-1,4,5,6-tetrahydro-N-methylpyridine 

Relevant academic research and scientific papers

A Pd(0)-mediated indole (macro)cyclization reaction

Herein we report a systematic study of the Larock indole annulation designed to explore the scope and define the generality of its use in macrocyclization reactions, its use in directly accessing the chloropeptin I versus II DEF ring system as well as key

Tandem radical cyclisations: Synthesis of lysergic acid derivatives

A novel free radical cyclisation approach for the synthesis of lysergic acid analogues has been investigated. The homolytic cleavage of carbon- bromine bond, mediated by tri-n-butyltin hydride, led to the development of a method for the construction of 3,