882048-84-2

Upstream product

• 882048-55-7 3'-O-tert-butyldimethylsilyl-N-(p-methoxyphenyl)-O-(tetrahydro-2''H-pyran-2''-yl)-N-trifluoroacetyl-α-vinyl-m-tyrosinol 
• 882048-19-3 (E)-3-(3'-tert-butyldimethylsilyloxy)-benzyl-4-O-(tetrahydro-2'H-pyran-2'-yl)-2-buten-1,4-diol 
• 131362-25-9 [3-(bromomethyl)-phenoxy]dimethyl(1,1-dimethylethyl)silane 

Downstream Products

• 882048-85-3 N-(p-methoxyphenyl)-O-(tetrahydro-2''H-pyran-2''-yl)-N-trifluoroacetyl-3'-O-triisopropylsilyl-α-vinyl-m-tyrosinol 
• 882048-73-9 3'-O-triisopropylsilyl-α-vinyl-m-tyrosinol 
• 882048-66-0 N-(p-methoxyphenyl)-O-(tetrahydro-2''H-pyran-2''-yl)-3'-O-triisopropylsilyl-α-vinyl-m-tyrosinol 
• 882048-77-3 N-(9-fluorenylmethoxycarbonyl)-3'-O-triisopropylsilyl-α-vinyl-m-tyrosinol 
• 882048-81-9 N-(9-fluorenylmethoxycarbonyl)-3'-O-triisopropylsilyl-α-vinyl-m-tyrosine 
• 70118-17-1 α-vinyl-m-tyrosine 

Relevant academic research and scientific papers

A formal [3,3]-sigmatropic rearrangement route to quaternary α-vinyl amino acids: Use of allylic N-PMP trifluoroacetimidates

Pd(II)-mediated rearrangement of allylic N-PMP (p-methoxyphenyl) trifluoroacetimidates provides the first formal sigmatropic route to quaternary, α-vinylic amino acids, potential suicide substrates for PLP enzymes. The amino acid side chains enter via tra