24164-73-6Relevant articles and documents
Synthesis of N-methyl L-phenylalanine for total synthesis of pepticinnamin e
Sun, Dequn,Zhang, Lingzi,Wang, Jin
, p. 319 - 322 (2012/09/07)
The target compounds 3, 10 and 11 were synthesized through different N-methylation strategies. The concise and efficient preparation of them in large scale was developed and 3, 10 and 11 were obtained in suitable form used for both nitrogen-end and oxygen-end extension in next coupling reaction in peptides synthesis, specifically in total synthesis of natural pepticinnamin E.
Antibacterial cyclopeptide alkaloids from the bark of Condalia buxifolia.
Morel, Ademir F,Araujo, Carla A,da Silva, Ubiratan F,Hoelzel, Solange C S M,Zachia, Renato,Bastos, Nelci R
, p. 561 - 566 (2007/10/03)
The cyclopeptide alkaloid, named condaline-A, was isolated from the root bark of Condalia buxifolia Reissek (Rhamnaceae), along with the known compounds adouetine-Y', scutianine-B, and scutianine-C. Their structures were determined by spectroscopic analys
Novel formation and crystal structure of 2-(2,2,2-trifluoroethylidene)-6-trifluoro-methyl-2,3-dihydro-4H-1,4-oxazin-3- ones from N-acetyl-N-alkyl-α-amino acids
Kawase, Masami,Saito, Setsuo,Kikuchi, Hiroyuki,Miyamae, Hiroshi
, p. 2185 - 2195 (2007/10/03)
The title compounds (2a-g) were formed from N-acetyl-N-alkyl-α-amino acids (1a-g) on treatment with trifluoroacetic anhydride in the presence of pyridine. The structure of the product (2a) was determined by single crystal X-Ray analysis.