research article

A novel synthesis of K-13

Beugelmans, Rene
•
Bigot, Antony
•
Zhu, Jieping  
1994
Tetrahedron Letters

A new and concise synthesis of the 17-membered macrocyclic tripeptide K-13 is achieved featuring an intramol. SNAr reaction as a key step. [on SciFinder (R)]

Type
research article
DOI
10.1016/0040-4039(94)85322-3
Author(s)
Beugelmans, Rene
Bigot, Antony
Zhu, Jieping  
Date Issued

1994

Publisher

Elsevier

Published in
Tetrahedron Letters
Volume

35

Issue

40

Start page

7391

End page

4

Subjects

Ring closure and formation (A novel synthesis of K-13 via intramol. SNAr reaction)

•

K13 total synthesis; ring closure K13 total synthesis

Note

CAN 122:82023

34-3

Amino Acids, Peptides, and Proteins

Inst. Chimie Substances Naturelles,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

446-34-4; 3978-80-1; 17355-19-0; 109838-85-9; 131858-37-2 Role: RCT (Reactant), RACT (Reactant or reagent) (A novel synthesis of K-13 via intramol. SNAr reaction); 160247-84-7P; 160247-85-8P; 160247-87-0P; 160247-88-1P; 160247-89-2P; 160247-90-5P; 160247-91-6P; 160247-92-7P; 161697-32-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (A novel synthesis of K-13 via intramol. SNAr reaction); 108890-90-0P (K-13); 160247-86-9P Role: SPN (Synthetic preparation), PREP (Preparation) (A novel synthesis of K-13 via intramol. SNAr reaction)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58573