Microwave-enhanced alpha-functionalisation of tetramates
Bicyclic tetramic acids may be efficiently allylated or arylated either directly or via the corresponding triflate, using a microwave-enhanced protocol; under these conditions, the yield and diastereoselectivity are very high. © Georg Thieme Verlag Stuttgart.
Главные авторы: | Moloney, M, Yaqoob, M |
---|---|
Формат: | Journal article |
Язык: | English |
Опубликовано: |
2008
|
Схожие документы
-
Functionalised bicyclic tetramates derived from cysteine as antibacterial agents.
по: Panduwawala, TD, и др.
Опубликовано: (2019) -
Chemoselective formation and reaction of densely functionalised bicyclic tetramic acids and their biological activity
по: Moloney, M, и др.
Опубликовано: (2017) -
Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives
по: Andrews, MD, и др.
Опубликовано: (1998) -
Novel chiral skeletons for drug discovery: antibacterial tetramic acids.
по: Holloway, C, и др.
Опубликовано: (2011) -
Stereoselectivity in the reduction of bicyclic tetramates
по: Josa-Cullere;, L, и др.
Опубликовано: (2016)