共 10 条
- [1] Wolff rearrangement of Nα-protected α-aminodiazoketones in presence of substituted phenol as a method for the synthesis of 2,4,5-trichlorophenyl esters of Fmoc-/Boc-/Z-β-homoamino acids PROTEIN AND PEPTIDE LETTERS, 2000, 7 (01): : 33 - 36
- [2] Synthesis of Boc- and Z-protected amino acid fluorides employing DAST as a fluorinating agent INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY, 2000, 39 (05): : 384 - 386
- [3] Convenient and efficient synthesis of Boc-/Z-/Fmoc-β-amino acids employing N-protected α-amino acid fluorides JOURNAL OF PEPTIDE RESEARCH, 2000, 55 (04): : 289 - 294
- [5] Synthesis of Nα-tetrachlorophthaloyl (TCP)-protected amino acids under microwave irradiation (MWI) SYNTHESIS-STUTTGART, 2001, (09): : 1313 - 1320
- [6] Wolff rearrangement of diazo ketones derived from N-p-tolylsulfonyl-protected α- and β-amino acids JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1998, (12): : 1919 - 1923
- [7] Microwave Assisted Alcoholysis of Isocyanates Derived from Nα-[(9-fluorenylmethyl)oxy]carbonyl Amino Acids: Synthesis of N-Fmoc-N1-Z-/Boc-/Alloc-/Bsmoc-gem-diamines International Journal of Peptide Research and Therapeutics, 2007, 13 : 393 - 397