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.
Автори: | Moloney, M, Yaqoob, M |
---|---|
Формат: | Journal article |
Мова: | English |
Опубліковано: |
2008
|
Схожі ресурси
Схожі ресурси
-
Functionalised bicyclic tetramates derived from cysteine as antibacterial agents.
за авторством: Panduwawala, TD, та інші
Опубліковано: (2019) -
Chemoselective formation and reaction of densely functionalised bicyclic tetramic acids and their biological activity
за авторством: Moloney, M, та інші
Опубліковано: (2017) -
Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives
за авторством: Andrews, MD, та інші
Опубліковано: (1998) -
Novel chiral skeletons for drug discovery: antibacterial tetramic acids.
за авторством: Holloway, C, та інші
Опубліковано: (2011) -
Stereoselectivity in the reduction of bicyclic tetramates
за авторством: Josa-Cullere;, L, та інші
Опубліковано: (2016)