scholarly journals Traceless Solid-Phase Synthesis of Ketones via Acid-Labile Enol Ethers: Application in the Synthesis of Natural Products and Derivatives

Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1406 ◽  
Author(s):  
Eva Schütznerová ◽  
Anna Krchňáková ◽  
Viktor Krchňák

In solid-phase organic synthesis, Wang resin is traditionally used for the immobilization of acids, alcohols, phenols, and amines. We report the use of Wang resin for the traceless synthesis of ketones via acid-labile enol ethers. We demonstrate the practicality of this synthetic strategy on the solid-phase synthesis of pyrrolidine-2,4-diones, which represent the core structure of several natural products, including tetramic acid. Base-triggered condensation of pyrrolidine-2,4-diones yielded 4-hydroxy-1,1′,2′,5-tetrahydro-2H,5′H-[3,3′-bipyrrole]-2,5′-diones.

2018 ◽  
Vol 360 (19) ◽  
pp. 3693-3699 ◽  
Author(s):  
Eva Schütznerová ◽  
Allen G. Oliver ◽  
Adam Přibylka ◽  
Viktor Krchňák

1992 ◽  
Vol 57 (8) ◽  
pp. 1707-1718
Author(s):  
Wolfgang Voelter ◽  
Gerhard Breipohl ◽  
Chryssa Tzougraki ◽  
Eveline Jungfleisch-Turgut

The solid phase synthesis of an amidated somatostatin analogue based on the principle of differentiated acidolysis is described. The acid labile and smoothly cleavable t-Bumeoc moiety (1% TFA/DCM) is used for temporary Nα-protection of D- and L-amino acids and [4-[[[9H-fluoren-9-yl-methoxycarbonyl]amino](4-methoxyphenyl)methyl]-2-methylphenoxy]acetic acid, attached to an aminomethylated polystyrene resin is used as acid sensitive linker of the solid carrier which releases the peptide in its amide form by treatment with TFA. Its preparation is described in detail.


Peptides ◽  
1992 ◽  
pp. 601-602 ◽  
Author(s):  
Roger J. Bontems ◽  
Peter Hegyes ◽  
Susan L. Bontems ◽  
Fernando Albericio ◽  
George Barany

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