Title of article :
The aza-Diels–Alder reaction protocol—a useful approach to chiral, sterically constrained α-amino acid derivatives
Author/Authors :
Sophie K Bertilsson، نويسنده , , Jenny K Ekegren، نويسنده , , Stefan A Modin، نويسنده , , Pher G Andersson، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2001
Pages :
8
From page :
6399
To page :
6406
Abstract :
Different types of polycyclic α-amino acid derivatives are prepared from chiral imines by using well-established aza-Diels–Alder reaction conditions. Simply by varying the diene moiety, different products such as spirocyclic compounds 8 and 9, anthracene 10, and tetrahydroquinolines 15–21 are formed.
Keywords :
aza-Diels–Alder reaction , tetrahydroquinoline , ?-amino acid , Anthracene
Journal title :
Tetrahedron
Serial Year :
2001
Journal title :
Tetrahedron
Record number :
1082245
Link To Document :
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