Stereoselective synthesis of (−)-desethyleburnamonine, (−)-vindeburnol and (−)-3-epitacamonine: observation of a substrate dependent diastereoselectivity reversal of an aldol reaction
2016 ◽
Vol 14
(44)
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pp. 10394-10406
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(−)-Acetoxyglutarimide was used for synthesis of target compounds wherein an acetoxy group induced enantioselectivity and functioned as a source of ketones.
2014 ◽
Vol 356
(16)
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pp. 3370-3376
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Keyword(s):
1992 ◽
Vol 57
(5)
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pp. 1324-1326
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2018 ◽
Vol 84
(2)
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pp. 1079-1084
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Keyword(s):
2002 ◽
Vol 67
(10)
◽
pp. 3231-3234
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Keyword(s):