Enantioselective total synthesis of (-)-xialenon A.

The first total synthesis of (-)-xialenon A (1) via conjugate allylation of a 1,5-cyclooctadiene-derived bicyclo[3.3.0]octenone 3 and an alpha'-hydroxylation on the more hinderd face of enone 9 using hypervalent iodine chemistry, is described.

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Hodgson, D, Galano, J, Christlieb, M
التنسيق: Journal article
اللغة:English
منشور في: 2002
الوصف
الملخص:The first total synthesis of (-)-xialenon A (1) via conjugate allylation of a 1,5-cyclooctadiene-derived bicyclo[3.3.0]octenone 3 and an alpha'-hydroxylation on the more hinderd face of enone 9 using hypervalent iodine chemistry, is described.