Direktes Verfahren zur Synthese vonN-Boc-L-3,4-Didehydroprolin
1980; Wiley; Volume: 92; Issue: 9 Linguagem: Alemão
10.1002/ange.19800920931
ISSN1521-3757
AutoresJean‐Robert Dormoy, Bertrand Castro, Georges Chappuis, U. Fritschi, P. Grogg,
Tópico(s)Chemical Synthesis and Reactions
ResumoAngewandte ChemieVolume 92, Issue 9 p. 761-761 Zuschrift Direktes Verfahren zur Synthese von N-Boc-L-3,4-Didehydroprolin† Dr. Jean-Robert Dormoy, Dr. Jean-Robert Dormoy Laboratoire de Chimie Organique II, Université de Nancy I Case officielle 140, F-54037 Nancy (Frankreich)Search for more papers by this authorProf. Dr. Bertrand Castro, Prof. Dr. Bertrand Castro Laboratoire de Chimie Organique II, Université de Nancy I Case officielle 140, F-54037 Nancy (Frankreich)Search for more papers by this authorDr. Georges Chappuis, Dr. Georges Chappuis Bachem Feinchemikalien AG CH-4416 Bubendorf (Schweiz)Search for more papers by this authorUlrich-Stefan Fritschi, Ulrich-Stefan Fritschi Bachem Feinchemikalien AG CH-4416 Bubendorf (Schweiz)Search for more papers by this authorDr. Peter Grogg, Dr. Peter Grogg Bachem Feinchemikalien AG CH-4416 Bubendorf (Schweiz)Search for more papers by this author Dr. Jean-Robert Dormoy, Dr. Jean-Robert Dormoy Laboratoire de Chimie Organique II, Université de Nancy I Case officielle 140, F-54037 Nancy (Frankreich)Search for more papers by this authorProf. Dr. Bertrand Castro, Prof. Dr. Bertrand Castro Laboratoire de Chimie Organique II, Université de Nancy I Case officielle 140, F-54037 Nancy (Frankreich)Search for more papers by this authorDr. Georges Chappuis, Dr. Georges Chappuis Bachem Feinchemikalien AG CH-4416 Bubendorf (Schweiz)Search for more papers by this authorUlrich-Stefan Fritschi, Ulrich-Stefan Fritschi Bachem Feinchemikalien AG CH-4416 Bubendorf (Schweiz)Search for more papers by this authorDr. Peter Grogg, Dr. Peter Grogg Bachem Feinchemikalien AG CH-4416 Bubendorf (Schweiz)Search for more papers by this author First published: September 1980 https://doi.org/10.1002/ange.19800920931Citations: 4 † Dehydroaminosäuren, 1. Mitteilung AboutPDF ToolsRequest permissionAdd to favorites ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Abstract Natürlich vorkommendes L-4-Hydroxyprolin als Edukt der Titelverbindung (1) ermöglicht eine viel einfachere Synthese als ältere Verfahren, die eine Racematspaltung erforderten. Schlüsselschritt ist die Pyrolyse des veresterten und in das S-Methyl-xanthogenat umgewandelten Edukts. Citing Literature Volume92, Issue9September 1980Pages 761-761 This is the German version of Angewandte Chemie. Note for articles published since 1962: Do not cite this version alone. Take me to the International Edition version with citable page numbers, DOI, and citation export. We apologize for the inconvenience. RelatedInformation
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