Highly Enantioselective Access to Primary Propargylamines: 4-Piperidinone as a Convenient Protecting Group

Highly Enantioselective Access to Primary Propargylamines: 4-Piperidinone as a Convenient Protecting Group

ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform , please click on HTML or PDF.

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Bibliographische Detailangaben
Veröffentlicht in:ChemInform 2006-10, Vol.37 (40), p.no-no
Hauptverfasser: Aschwanden, Patrick, Stephenson, Corey R. J., Carreira, Erick M.
Format: Artikel
Sprache:eng
Schlagworte:
amination
amination, N‐alkylation, N‐arylation
amines (acyclic compounds)
amines (benzene compounds)
deprotection
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
multicomponent reactions
N-alkylation
N-arylation
protection
protection, deprotection
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Beschreibung
Zusammenfassung:ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform , please click on HTML or PDF.
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.200640037