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1986
DOI: 10.1016/s0040-4039(00)83885-x
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Synthesis of α-amino-β-hydroxy acids using -bis(trimethylsilyl)aminoketene bis(trimethylsilyl) acetal or its -methyl--trimethylsilyl analog

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Cited by 16 publications
(2 citation statements)
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“…The selectivity is not high when tert -butyl N,N -dimethylglycinate is the ester substrate. In contrast, trimethylsilyl N,N- bis(trimethylsilyl)glycinate ( 9 ) exclusively gave the ancat product 10 (Scheme ). , ( Ancat and syncat have been used as defined by Carey 6 …”
Section: A From Amino Acidsmentioning
confidence: 99%
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“…The selectivity is not high when tert -butyl N,N -dimethylglycinate is the ester substrate. In contrast, trimethylsilyl N,N- bis(trimethylsilyl)glycinate ( 9 ) exclusively gave the ancat product 10 (Scheme ). , ( Ancat and syncat have been used as defined by Carey 6 …”
Section: A From Amino Acidsmentioning
confidence: 99%
“…In contrast, trimethylsilyl N,N-bis(trimethylsilyl)glycinate (9) exclusively gave the ancat product 10 (Scheme 6). 40,41 (Ancat and syncat have been used as defined by Carey. 42 ) R-Amino esters can be converted to the corresponding imines; a popular choice is the imine 11 derived from benzophenone.…”
Section: A Introductionmentioning
confidence: 99%