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22
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0344311826
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23 was low-yielding in the presence of the acyl camphor sultam
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23 was low-yielding in the presence of the acyl camphor sultam.
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23
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0000986355
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24
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0037988256
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The cycloreversion of phenyl-substituted isoxazolidines to release cyclic nitrones in situ appears to be novel, although it has recently been used to regenerate a nitrone by flash pyrolysis. See Coskun, N.; Ay, M. Heterocycles 1998, 48, 537.
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Coskun, N.1
Ay, M.2
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25
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0001647908
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2 was used to generate the ylid at -30 °C, and the precipitated potassium salts were then removed to give a salt-free, yellow solution of the ylid which was added via cannula to a solution of the aldehyde in THF at -78 °C
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2 was used to generate the ylid at -30 °C, and the precipitated potassium salts were then removed to give a salt-free, yellow solution of the ylid which was added via cannula to a solution of the aldehyde in THF at -78 °C.
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Stork, G.1
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9644285669
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Sonogashira, R.K.1
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Hagihara, N.3
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28
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0345174276
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Cleavage of the N-O bond in the presence of the desilylated enynes was accompanied by reduction of the acetylenic groups to give a mixture of HTX, dihydro-HTX, neodihydro-HTX, and tetrahydro-HTX
-
Cleavage of the N-O bond in the presence of the desilylated enynes was accompanied by reduction of the acetylenic groups to give a mixture of HTX, dihydro-HTX, neodihydro-HTX, and tetrahydro-HTX.
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29
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0344744165
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note
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2 = 0.837.
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