The stereoselective total synthesis of isocladosorpin
2013
Reddy, B.V Subba | Reddy, P Janardhan | Reddy, C Suresh
A highly stereoselective total synthesis of isocladosorpin is described. The key steps involved in this synthesis are oxa-Michael reaction, asymmetric propargylation, and Alder–Rickerts reaction.
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Bibliographic information
Publisher
Elsevier B.V.
Other Subjects
Oxa-michael reaction; Isocladosorpin; Alder–rickerts reaction; Asymmetric propargylation
Language
English
Type
Journal Article; Text
2024-02-27
MODS
Data Provider
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