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Highly Diastereoselective Dioxetane Formation in the Photooxygenation of Enecarbamates with an Oxazolidinone Chiral Auxiliary: Steric Control in the [2 + 2] Cycloaddition of Singlet Oxygen through Conformational Alignment

โœ Scribed by Adam, Waldemar; Bosio, Sara G.; Turro, Nicholas J.

Book ID
126274539
Publisher
American Chemical Society
Year
2002
Tongue
English
Weight
51 KB
Volume
124
Category
Article
ISSN
0002-7863

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๐Ÿ“œ SIMILAR VOLUMES

Enecarbamates as Selective Substrates in
Enecarbamates as Selective Substrates in Oxidations: Chiral-Auxiliary-Controlled Mode Selectivity and Diastereoselectivity in the [2 + 2] Cycloaddition and Ene Reaction of Singlet Oxygen and in the Epoxidation by DMD and mCPBA.
โœ Waldemar Adam; Sara G. Bosio; Nicholas J. Turro; Barbara T. Wolff ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons โš– 310 KB ๐Ÿ‘ 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.