Tetrahedron letters

Synthese stereospecifique de l'ester methylique de l'acide amino-2 oxo-8 epoxy-9, 10 decanoique (2s, 9r) N-protege.

R Jacquier, R Lazaro, H Raniriseheno, P Viallefont

Index: Jacquier, R.; Lazaro, R.; Raniriseheno, H.; Viallefont, P. Tetrahedron Letters, 1984 , vol. 25, # 48 p. 5525 - 5528

Full Text: HTML

Citation Number: 13

Abstract

Abstract The first stereospecific synthesis of methyl (2S, 9R) N-tBOC 2-amino 8-oxo 9, 10- epoxydecanoate has been carried out by using two steps allowing a chirality control: a stereospecific alkylation of the Schiff base 4 and Sharpless epoxidation of the allylic alcohol 6.

Related Articles:

Synthesis of (5Z)-5, 13-tetradecadien-1-yl acetate and (3E, 5Z)-3, 5, 13-tetradecatrien-1-yl acetate (the secretion of the larvae of the lepidopterous Cossus …

[Garanti,L. et al. Gazzetta Chimica Italiana, 1976 , vol. 106, p. 187 - 196]

Synthesis of (5Z)-5, 13-tetradecadien-1-yl acetate and (3E, 5Z)-3, 5, 13-tetradecatrien-1-yl acetate (the secretion of the larvae of the lepidopterous Cossus …

[Garanti,L. et al. Gazzetta Chimica Italiana, 1976 , vol. 106, p. 187 - 196]

Total synthesis of viridiofungin A

[Morokuma, Kenji; Takahashi, Keisuke; Ishihara, Jun; Hatakeyama, Susumi Chemical Communications, 2005 , # 17 p. 2265 - 2267]

More Articles...