The Intramolecular Buchner Reaction of α-Diazo-β-Ketonitriles: Development and Application to the Total Synthesis of (+)-Salvileucalin B

The Intramolecular Buchner Reaction of α-Diazo-β-Ketonitriles: Development and Application to the Total Synthesis of (+)-Salvileucalin B

<p>Since its discovery in 1896, the Buchner reaction has fascinated chemists for more than a century. The highly reactive nature of the carbene intermediates allows for facile dearomatization of stable aromatic rings, and provides access to a diverse array of cyclopropane and seven-membered ri...

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Bibliographic Details
Main Author: Nani, Roger Rauhauser
Format: Others
Published: 2013
Online Access:https://thesis.library.caltech.edu/7847/1/Nani-R-R-2013thesis.pdf
Nani, Roger Rauhauser (2013) The Intramolecular Buchner Reaction of α-Diazo-β-Ketonitriles: Development and Application to the Total Synthesis of (+)-Salvileucalin B. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/2KGP-7X92. https://resolver.caltech.edu/CaltechTHESIS:06062013-031825238 <https://resolver.caltech.edu/CaltechTHESIS:06062013-031825238>

Internet

https://thesis.library.caltech.edu/7847/1/Nani-R-R-2013thesis.pdf
Nani, Roger Rauhauser (2013) The Intramolecular Buchner Reaction of α-Diazo-β-Ketonitriles: Development and Application to the Total Synthesis of (+)-Salvileucalin B. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/2KGP-7X92. https://resolver.caltech.edu/CaltechTHESIS:06062013-031825238 <https://resolver.caltech.edu/CaltechTHESIS:06062013-031825238>

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