Long-Range Diastereoselectivity in an Ugi Reaction: Stereocontrolled and Diversity-Oriented Synthesis of Tetrahydrobenzoxazepines
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Title
Long-Range Diastereoselectivity in an Ugi Reaction: Stereocontrolled and Diversity-Oriented Synthesis of Tetrahydrobenzoxazepines
Authors
Keywords
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Journal
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2013, Issue 23, Pages 5064-5075
Publisher
Wiley
Online
2013-07-02
DOI
10.1002/ejoc.201300541
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Note: Only part of the references are listed.- Recent Advances in Asymmetric Isocyanide-Based Multicomponent Reactions
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- Asymmetric synthesis of synthetic alkaloids by a tandem biocatalysis/Ugi/Pictet–Spengler-type cyclization sequence
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- A Marriage of Convenience: Combining the Power of Isocyanide-Based Multicomponent Reactions with the Versatility of (Hetero)norbornene Chemistry
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- Solvent effects on stereoselectivity: more than just an environment
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