Title of article :
En route to sugar–alkaloid conjugates Original Research Article
Author/Authors :
Carsten-Endres Sowa، نويسنده , , Joachim Thiem، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2011
Pages :
5
From page :
1546
To page :
1550
Abstract :
After stereoselective addition of N-iodosuccinimide to glycals subsequent dehalogenation results in formation of N-glycopyranosyl succinimides. By UV irradiation both azepindiones and preferentially [5.3.1.02,6] tricyclic oxalactams could be obtained. Their transformation into a number of novel sugar conjugates resembling some prominent alkaloid N-pyrrol components by thiation and reduction is reported.
Keywords :
Simplexin oxa-analogs , Glycopyranosyl-N-pyrrol , N-2-Deoxyglycopyranosyl succinimides , 2 , 6] Oxalactams
Journal title :
Carbohydrate Research
Serial Year :
2011
Journal title :
Carbohydrate Research
Record number :
967217
Link To Document :
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