Tetrahedron Letters

Stereoselectivity in micellar and vesicular reactions

RA Moss, T Taguchi, GO Bizzigotti

Index: Moss, Robert A.; Taguchi, Takayuki; Bizzigotti, George O. Tetrahedron Letters, 1982 , vol. 23, # 19 p. 1985 - 1988

Full Text: HTML

Citation Number: 15

Abstract

Abstract The diastereoselectivity of esterolytic cleavage of certain dipeptide and tripeptide activated esters is lower in thiol-functionalized vesicles than in comparable micelles. This is thought to be a mechanism-specific effect related to the greater molecular ordering in vesicular systems.

Related Articles:

Convenient synthesis of C-terminal di-and tri-peptide amides from N-protected dipeptidoylbenzotriazoles

[Celik, Ilhami; Abdel-Fattah, Ashraf A.A. Tetrahedron, 2009 , vol. 65, # 25 p. 4923 - 4929]

The efficient preparation of di-and tripeptides by coupling N-(Cbz-or Fmoc-α-aminoacyl) benzotriazoles with unprotected amino acids

[Katritzky, Alan R.; Angrish, Parul; Suzuki, Kazuyuki Synthesis, 2006 , # 3 p. 411 - 424]

More Articles...