EFFICIENT SYNTHESIS OF 3-MONO AND DISUBSTITUTED LACTAMS USING MEERWEIN-ESCHENMOSER [3,3] SIGMATROPIC REARRANGEMENTS

Autoria(s): COATES, B; MONTGOMERY, DJ; STEVENSON, PJ; Stevenson, Paul
Data(s)

28/03/1994
Resumo

<p>3-Allyl substituted five six and seven membered ring lactams, are readily available in good yields and reasonable selectivity by a formal Meerwein Eschenmoser [3,3] rearrangement, using readily available methoxymethyleniminium salts and lithium alkoxides derived from allyl alcohols.</p>
Identificador

http://pure.qub.ac.uk/portal/en/publications/efficient-synthesis-of-3mono-and-disubstituted-lactams-using-meerweineschenmoser-33-sigmatropic-rearrangements(ff588331-e4d8-4f02-a85a-92aa297f8734).html
Idioma(s)

eng
Direitos

info:eu-repo/semantics/restrictedAccess
Fonte

COATES , B , MONTGOMERY , D J , STEVENSON , P J & Stevenson , P 1994 , ' EFFICIENT SYNTHESIS OF 3-MONO AND DISUBSTITUTED LACTAMS USING MEERWEIN-ESCHENMOSER [3,3] SIGMATROPIC REARRANGEMENTS ' Tetrahedron , vol 50 , no. 13 , pp. 4025-4036 .
Palavras-Chave #STEREOCHEMICAL CONTROL #CLAISEN REARRANGEMENT
Tipo

article
Acesso ao item digital