Preparation of enantioenriched iodinated pyrrolinones by iodocyclization of α-amino-ynones-Reference-Cited by-同舟云学术

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Preparation of enantioenriched iodinated pyrrolinones by iodocyclization of α-amino-ynones

Published:2012 Issue:45 Volume:10 Page:9085
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Spina Rosella,Colacino Evelina,Gabriele Bartolo,Salerno Giuseppe,Martinez Jean,Lamaty Frédéric

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB26427G

Reference44 articles.

1. The use ofN-urethane-protectedN-carboxyanhydrides (UNCAs) in amino acid and peptide synthesis

2. Urethane-protected α-amino acid N-carboxyanhydrides and peptide synthesis

3. Solvent-Free Synthesis of Peptides

4. Synthesis of chiral N-protected α-amino aldehydes by reduction of N-protected N-carboxyanhydrides (UNCAs)

5. Diastereoselective Synthesis of N-Protected β-Amino-α-hydroxyacids (Norstatines) from Urethane N-Carboxyanhydrides (UNCAs)

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2. A dual mode ‘turn-on’ fluorescence-Raman (SERS) response probe based on a 1H-pyrrol-3(2H)-one scaffold for monitoring H₂S levels in biological samples;Analytical Methods;2023

3. Facile three-component reactions for the synthesis of N-unsubstituted 1H-pyrrol-3(2H)-ones and base induced divergent N–H and C–C bond derivatizations;Tetrahedron;2022-10

4. A micro-flow rapid dual activation approach for urethane-protected α-amino acid N-carboxyanhydride synthesis;Organic & Biomolecular Chemistry;2022

5. Sc(OTf)3-Catalyzed Iodocyclization/Ritter-Type Amidation of N-Alkoxypropiolamides: A Synthetic Strategy for Isoxazol-3(2H)-ones;The Journal of Organic Chemistry;2021-10-20

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