A convenient synthesis of N-Boc-protected tert-butyl esters of phenylglycines from benzylamines

[1]  S. E. D. Laszlo,et al.  Deprotection of N-tert-butoxycarbonyl (Boc) groups in the presence of tert-butyl esters , 2000 .

[2]  A. Giumanini,et al.  Deprotection of t-Butyl Esters of Amino Acid Derivatives by Nitric Acid in Dichloromethane , 2000 .

[3]  P. Váchal,et al.  Enantioselective catalytic addition of HCN to ketoimines. Catalytic synthesis of quaternary amino acids. , 2000, Organic letters.

[4]  J. Yoshida,et al.  Formation and reaction of 2-metalated N-Boc-4,4-dimethyl-1,3-oxazolidines in the presence of (−)-sparteine: new chiral formyl anion equivalents , 1998 .

[5]  O. Hara,et al.  Novel N → C acyl migration reaction of acyclic imides: A facile method for α-aminoketones and β-aminoalcohols , 1998 .

[6]  M. R. Gagné,et al.  A Mild Protocol for the Conversion of Simple Esters to tert-Butyl Esters. , 1997, The Journal of organic chemistry.

[7]  S. Wright,et al.  Convenient preparations of t-butyl esters and ethers from t-butanol , 1997 .

[8]  C. Barberis,et al.  Enantioselective synthesis of phenylglycines using (−) sparteine•s-BuLi complex , 1997 .

[9]  P. Beak,et al.  Enantioselective Syntheses of α-, β-, and γ-Aryl Amino Acids and Esters , 1997 .

[10]  D. Ager,et al.  1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis. , 1996, Chemical reviews.

[11]  Mitsuru Watanabe,et al.  Stereoselective Synthesis of trans-4,5-Disubstituted 1,3-Imidazolidin-2-ones by Reaction of an alpha-Nitrogen Carbanion with Imines. , 1996, The Journal of organic chemistry.

[12]  D. Limat,et al.  Sparteine-mediated .alpha.-lithiation of N-BOC-N-methylbenzylamine: Rapid racemization and subsequent deracemization. , 1995 .

[13]  N. Voyer,et al.  An expedient enantioselective synthesis of N-t-Boc-Protected Phenylsarcosine. , 1995 .

[14]  H. Rapoport,et al.  Selective Removal of an N-BOC Protecting Group in the Presence of a tert-Butyl Ester and Other Acid-Sensitive Groups , 1994 .

[15]  Robert M. Williams.  Synthesis of optically active α-amino acids , 1989 .

[16]  H. Musso,et al.  New Naturally Occurring Amino Acids , 1983 .

[17]  P. Hodge,et al.  Protective groups in organic synthesis , 1981 .

[18]  S. Raucher,et al.  Organoselenium chemistry. 4. Deprotonations with potassium diisopropylamide-lithium tert-butoxide. Alkylation of 1-(phenylseleno)alkenes and bis(phenylseleno) acetals , 1978 .

[19]  I. Stirling,et al.  Selective removal of the -butyloxycarbonyl protecting group in the presence of t-butyl and p-methoxybenzyl esters , 1975 .

[20]  R. Hiskey,et al.  Sulfur-containing polypeptides. XV. Synthetic routes to the A 6-13 segment of ovine insulin. , 1972, The Journal of organic chemistry.

[21]  A. M. Khoujah,et al.  Selective cleavage of the t-butyloxycarbonyl protecting group , 1969 .