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- Stereoselection in the synthesis of threo- and erythro-3-amino-2-hydroxy-4-phenyl-butanoic acid using chiral acetal templates. Rosario Herranz, Julia Castro-Pichel, Soledad Vinuesa, M. Teresa García-López
, J. Chem. Soc., Chem. Commun.
, 1989
, 938
- Regio- and stereo-specific synthesis of threo-3-amino-2-hydroxy-acids, novel amino-acids contained in aminopeptidase inhibitors of microbial origin. Kuniki Kato, Tetsushi Saino, Rinzo Nishizawa, Tomohisa Takita, Hamao Umezawa
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 1618
- A case study of the MAC (masked acyl cyanide) oxyhomologation of N,N-dibenzyl-l-phenylalaninal with anti diastereoselectivity: preparation of (2S,3S)-allophenylnorstatin esters. Xuefeng He, Marie Buchotte, Régis Guillot, Sandrine Deloisy, David J. Aitken
, Org. Biomol. Chem.
, 2022
, 20
, 1769
- Recent advances in the total synthesis of polyhydroxylated alkaloids via chiral oxazines. Seokhwi Park, In-Soo Myeong, Won-Hun Ham
, Org. Biomol. Chem.
, 2024
, 22
, 894
- Novel and efficient synthesis of difficult sequence-containing peptides through O–N intramolecular acyl migration reaction of O-acyl isopeptides. Youhei Sohma, Masato Sasaki, Yoshio Hayashi, Tooru Kimura, Yoshiaki Kiso
, Chem. Commun.
, 2004
, 124