- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Cyclopeptide Synthesis by Ring-Closing Metathesis ; volume:18 ; number:05 ; year:2022 ; pages:0565
Synfacts ; 18, Heft 05 (2022), 0565
- DOI
-
10.1055/s-0041-1737572
- URN
-
urn:nbn:de:101:1-2022060911074495760320
- Rechteinformation
-
Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:31 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Ähnliche Objekte (12)
Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis
Olefin metathesis – ring-closing reaction
Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy
Ring-closing-metathesis-based synthesis of annellated coumarins from 8-allylcoumarins
Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis
Synthesis of macrocyclic lactams related to the antitumor antibiotic geldanamycin by ring closing metathesis
Synthesis of bioactive peptides and conformationally restricted analogs including ring closing metathesis : = Synthese von bioaktiven Peptiden und konformativ eingeschränkten Analoga inklusive Ring-Closing-Metathesis
A short stereoselective synthesis of (+)-(6R,2S)-cryptocaryalactone via ring-closing metathesis
Synthesis of Various Heterocycles Having a Dienamide Moiety by Ring-Closing Metathesis of Ene-ynamides
Functionalizable Stereocontrolled Cyclopolyethers by Ring‐Closing Metathesis as Natural Polymer Mimics
Functionalizable Stereocontrolled Cyclopolyethers by Ring‐Closing Metathesis as Natural Polymer Mimics
Ring closing metathesis : a gateway to medium size ring ethers
Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis
Olefin metathesis – ring-closing reaction
Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy
Ring-closing-metathesis-based synthesis of annellated coumarins from 8-allylcoumarins
Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis
Synthesis of macrocyclic lactams related to the antitumor antibiotic geldanamycin by ring closing metathesis
Synthesis of bioactive peptides and conformationally restricted analogs including ring closing metathesis : = Synthese von bioaktiven Peptiden und konformativ eingeschränkten Analoga inklusive Ring-Closing-Metathesis
A short stereoselective synthesis of (+)-(6R,2S)-cryptocaryalactone via ring-closing metathesis
Synthesis of Various Heterocycles Having a Dienamide Moiety by Ring-Closing Metathesis of Ene-ynamides
Functionalizable Stereocontrolled Cyclopolyethers by Ring‐Closing Metathesis as Natural Polymer Mimics
Functionalizable Stereocontrolled Cyclopolyethers by Ring‐Closing Metathesis as Natural Polymer Mimics
Ring closing metathesis : a gateway to medium size ring ethers
Synthesis of Berkeleylactone A by Ring‐Closing Alkyne Metathesis
Olefin metathesis – ring-closing reaction
Synthesis of Bioactive Macrocycles Involving Ring-Closing Metathesis Strategy
Ring-closing-metathesis-based synthesis of annellated coumarins from 8-allylcoumarins
Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis
Synthesis of macrocyclic lactams related to the antitumor antibiotic geldanamycin by ring closing metathesis
Synthesis of bioactive peptides and conformationally restricted analogs including ring closing metathesis : = Synthese von bioaktiven Peptiden und konformativ eingeschränkten Analoga inklusive Ring-Closing-Metathesis
A short stereoselective synthesis of (+)-(6R,2S)-cryptocaryalactone via ring-closing metathesis
Synthesis of Various Heterocycles Having a Dienamide Moiety by Ring-Closing Metathesis of Ene-ynamides
Functionalizable Stereocontrolled Cyclopolyethers by Ring‐Closing Metathesis as Natural Polymer Mimics
Functionalizable Stereocontrolled Cyclopolyethers by Ring‐Closing Metathesis as Natural Polymer Mimics