Tetrahedron Letters

Diastereoselective synthesis of 3-amino-1, 2-diols by reductive alkylation of 2, 3-dialkoxynitriles

P Hutin, M Larchevêque

Index: Tetrahedron Letters, , vol. 41, # 14 p. 2369 - 2372

Full Text: HTML

Citation Number: 3

Abstract

... Please enable JavaScript to use all the features on this page. Tetrahedron Letters. Volume 41, Issue 14, 1 April 2000, Pages 2369–2372. Cover image Cover image. ... 14 Moreover, this separation was facilitated by the fact that, in all cases, the all syn isomer 4 was eluted first. ...

Related Articles:

An efficient and highly chemoselective N-Boc protection of amines, amino acids, and peptides under heterogeneous conditions

[Jahani, Fatemeh; Tajbakhsh, Mahmood; Khaksar, Samad; Azizi, Mohamad Reza Monatshefte fur Chemie, 2011 , vol. 142, # 10 p. 1035 - 1043]

Highly practical methodology for the synthesis of d-and l-α-amino acids, N-protected α-amino acids, and N-methyl-α-amino acids

[Myers, Andrew G.; Gleason, James L.; Yoon, Taeyoung; Kung, Daniel W. Journal of the American Chemical Society, 1997 , vol. 119, # 4 p. 656 - 673]

Versatile routes to chiral 4-substituted 2-oxazolidinones and. ALPHA.-amino acids. Use of chiron,(4+ 2) cycloadducts of dialkyl azodicarboxylates and 2-oxazolones.

[Chemical and Pharmaceutical Bulletin, , vol. 40, # 4 p. 1077 - 1079]

Highly practical methodology for the synthesis of d-and l-α-amino acids, N-protected α-amino acids, and N-methyl-α-amino acids

[Journal of the American Chemical Society, , vol. 119, # 4 p. 656 - 673]

Highly practical methodology for the synthesis of d-and l-α-amino acids, N-protected α-amino acids, and N-methyl-α-amino acids

[Journal of the American Chemical Society, , vol. 119, # 4 p. 656 - 673]

More Articles...