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79951989613
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For more synthetic studies from the groups of Fuchs, Heathcock, Winterfeldt, Taber and Shair see ther following and references cited therein
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5
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8
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0037863136
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19
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79951962098
-
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CCDC 791575 contains the supplementary crystallographic data for 16.These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
CCDC 791575 contains the supplementary crystallographic data for 16.These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
-
-
-
-
21
-
-
79952000658
-
-
The 23(R) stereochemistry of the major adduct 4 was confirmed by X-ray crystallography of its 3-hydroxyl derivative (CCDC 791577, see Supporting Information)
-
The 23(R) stereochemistry of the major adduct 4 was confirmed by X-ray crystallography of its 3-hydroxyl derivative (CCDC 791577, see Supporting Information).
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22
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0343432002
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23
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79951975137
-
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The structure of 22 was confirmed by X-ray crystallography of its 3-silyl ether derivative (CCDC 791576, see Supporting Information)
-
The structure of 22 was confirmed by X-ray crystallography of its 3-silyl ether derivative (CCDC 791576, see Supporting Information).
-
-
-
-
27
-
-
79951999722
-
-
See Supporting Information for the synthesis of chiral aldehyde 27
-
See Supporting Information for the synthesis of chiral aldehyde 27.
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29
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0000423772
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79951984977
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Thioketal could be unmasked under cycloaddtion conditions, while removal of acid-sensitive protecting groups and E/F-ring ketalization could take place simultaneously during reductive cleavage of the O-O bond (Zn powder in HOAc)
-
Thioketal could be unmasked under cycloaddtion conditions, while removal of acid-sensitive protecting groups and E/F-ring ketalization could take place simultaneously during reductive cleavage of the O-O bond (Zn powder in HOAc).
-
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34
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25444498936
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N2' reaction to complete the functionalization of the D ring as the key transformation in their synthesis of south 7 hemisphere
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