Tetrahedron: Asymmetry

Efficient synthesis of benzyl 2-(S)-[(tert-butoxycarbonyl) amino]-ω-iodoalkanoates

Y Koseki, H Yamada, T Usuki

Index: Koseki, Yohei; Yamada, Haruka; Usuki, Toyonobu Tetrahedron Asymmetry, 2011 , vol. 22, # 5 p. 580 - 586

Full Text: HTML

Citation Number: 22

Abstract

Abstract The efficient synthesis of four benzyl 2-(S)-[(tert-butoxycarbonyl) amino]-ω- iodoalkanoates {benzyl 2-(S)-[(tert-butoxycarbonyl) amino]-3-iodopropanoate, benzyl 2-(S)- [(tert-butoxycarbonyl) amino]-4-iodobutanoate, benzyl 2-(S)-[(tert-butoxycarbonyl) amino]-5- iodopentanoate, benzyl 2-(S)-[(tert-butoxycarbonyl) amino]-6-iodohexanoate} from natural or protected l-amino acids is described.

Related Articles:

Synthesis of L-selenocystine, L-[77 Se] selenocystine and L-tellurocystine

[Stocking, Emily M.; Schwarz, Jessie N.; Senn, Hans; Salzmann, Michael; Silks, Louis A. Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 16 p. 2443 - 2447]

Preparation of enantiomerically pure protected 4-oxo. alpha.-amino acids and 3-aryl. alpha.-amino acids from serine

[Journal of Organic Chemistry, , vol. 57, # 12 p. 3397 - 3404]

Efficient synthesis of benzyl 2-(S)-[(tert-butoxycarbonyl) amino]-ω-iodoalkanoates

[Tetrahedron Asymmetry, , vol. 22, # 5 p. 580 - 586]

More Articles...