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Journal article
Peer reviewed
Synthesis of batzelladine E and its E isomer
Barry B Snider
and
Jinsheng Chen
Tetrahedron letters, Vol.39(32), pp.5697-5700
08/06/1998
DOI:
https://doi.org/10.1016/S0040-4039(98)01196-4
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Abstract
Biginelli reaction
guanidines
The synthesis of 4E established that batzelladine E (4Z) has the Z- rather than the E-stereochemistry previously depicted. Batzelladine E (4Z) has been synthesized by an efficient 9-step route in 3% overall yield.
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Title
Synthesis of batzelladine E and its E isomer
Creators
Barry B Snider
Jinsheng Chen
Publication Details
Tetrahedron letters, Vol.39(32), pp.5697-5700
Publisher
Elsevier Ltd
Identifiers
9924012825601921
Copyright
© 1998 Published by Elsevier Ltd.
Academic Unit
Department of Chemistry
Language
English
Resource Type
Journal article
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