A vitamin E derivative as a novel, extremely advantageous amino-protecting group

T Rosenau, CL Chen, WD Habicher

Index: Journal of Organic Chemistry, , vol. 60, # 25 p. 8120 - 8121

Full Text: HTML

Citation Number: 13

Abstract

... Page 2. Communications J. Org. Chem., Vol. 60, No. 25, 1995 8121 ... This procedure resembles the sequence presented in Scheme 1. N-Alkylation of amino acids is less common in syn- thetic organic chemistry than the coupling of amino acids to di- 'or oligopeptides. ...

Related Articles:

Lewis acid-promoted 3-aza-Cope rearrangement of N-alkyl-N-allyl enamines

[Cook, Gregory R.; Barta, Nancy S.; Stille, John R. Journal of Organic Chemistry, 1992 , vol. 57, # 2 p. 461 - 467]

Secondary amine formation from reductive amination of carbonyl compounds promoted by Lewis acid using the InCl3/Et3SiH system

[Organic Letters, , vol. 11, # 15 p. 3302 - 3305]

Lewis acid-promoted 3-aza-Cope rearrangement of N-alkyl-N-allyl enamines

[Journal of Organic Chemistry, , vol. 57, # 2 p. 461 - 467]

More Articles...