The homologation of aamino acids to ßamino acids by the twostep Arndt–Eister method is achieved by using Fmocaamino acid pentafluorophenyl esters for the acylation of diazomethane, synthesizing the key intermediates Fmocaminoacyldiazomethanes as crystalline solids in good yields and purity
A new and efficient method for the homologation of urethane protected alpha-amino acids to its beta-...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
A simple, efficient and stereospecific approach for the homologation of urethane-protected alpha-ami...
The homologation of alpha-amino acids to beta-amino acids by the two-step Arndt-Eister method is ach...
The Wolff rearrangement of alpha -aminodiazoketones derived from N-alpha-urethane protected alpha -a...
A simple, efficient and stereospecific approach for the homologation of urethane-protected a-amino a...
A new and efficient method for the synthesis of N-alpha-Fmoc-/Boc-/Z-beta-amino acids using the two-...
A new and efficient method for the synthesis of Nα-Fmoc-/Boc-/Z-β-amino acids using the two-st...
An efficient and stereospecific homologation of urethane-protected α-amino acids to β-amino acids ...
2152-2158An efficient and stereospecific homologation of urethane-protected α-amino acids to β-amin...
A simple approach for the homologation of α-amino acids to β-amino acids by the Arndt-Eistert meth...
The pentafluorophenyl esters of Boc-/Z-amino acids are used for the preparation of the key intermedi...
The use of Boc(2)O as a coupling agent in the homologation of N-urethane protected-alpha-amino acid ...
A new and efficient method for the synthesis ofNα-Fmoc-/Boc-/Z-β-amino acids using the two-step Arnd...
β-Amino acids X-NHCHRCH2CO2H (X = Z, Boc, or Fmoc protecting group; R = PhCH2, Me2CH, Ph, Me) were...
A new and efficient method for the homologation of urethane protected alpha-amino acids to its beta-...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
A simple, efficient and stereospecific approach for the homologation of urethane-protected alpha-ami...
The homologation of alpha-amino acids to beta-amino acids by the two-step Arndt-Eister method is ach...
The Wolff rearrangement of alpha -aminodiazoketones derived from N-alpha-urethane protected alpha -a...
A simple, efficient and stereospecific approach for the homologation of urethane-protected a-amino a...
A new and efficient method for the synthesis of N-alpha-Fmoc-/Boc-/Z-beta-amino acids using the two-...
A new and efficient method for the synthesis of Nα-Fmoc-/Boc-/Z-β-amino acids using the two-st...
An efficient and stereospecific homologation of urethane-protected α-amino acids to β-amino acids ...
2152-2158An efficient and stereospecific homologation of urethane-protected α-amino acids to β-amin...
A simple approach for the homologation of α-amino acids to β-amino acids by the Arndt-Eistert meth...
The pentafluorophenyl esters of Boc-/Z-amino acids are used for the preparation of the key intermedi...
The use of Boc(2)O as a coupling agent in the homologation of N-urethane protected-alpha-amino acid ...
A new and efficient method for the synthesis ofNα-Fmoc-/Boc-/Z-β-amino acids using the two-step Arnd...
β-Amino acids X-NHCHRCH2CO2H (X = Z, Boc, or Fmoc protecting group; R = PhCH2, Me2CH, Ph, Me) were...
A new and efficient method for the homologation of urethane protected alpha-amino acids to its beta-...
Coupling of Fmoc-amino acid chlorides mediated by activated commercial zinc dust for the synthesis o...
A simple, efficient and stereospecific approach for the homologation of urethane-protected alpha-ami...
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