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Journal ArticleDOI

Preference for photodissociation over internal [2 + 2]-cycloaddition during irradiation of an unsaturated α,β-enone

E. J. Corey, +1 more
- 01 Jan 1994 - 
- Vol. 35, Iss: 5, pp 663-664
TLDR
In this article, it was shown that irradiation of 2, its trimethylsilyl ether or acetate ester using ultraviolet light of wavelength > 290 nm results not in internal olefin cycloaddition, but exclusively in photodissociation either of the intercyclic bond (for 2 or the TMS ether) or the COAc bond for the acetates ester.
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This article is published in Tetrahedron Letters.The article was published on 1994-01-01. It has received 11 citations till now. The article focuses on the topics: Ultraviolet light & Cycloaddition.

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Journal ArticleDOI

Biocatalytic approaches towards the stereoselective synthesis of vicinal amino alcohols

TL;DR: This comprehensive report seeks to provide an overview of recent (chemo)enzymatic methods, focusing on the strategy employed (use of transaminases, kinetic resolution, dynamic kineticresolution, biocatalytic C–C bond formation or enantioconvergent processes) and the type ofBiocatalyst(s) used for the preparation of enantiopure vicinal amino alcohols.
Journal ArticleDOI

Cyclic trans-β-amino alcohols: preparation and enzymatic kinetic resolution

TL;DR: In this article, enantioenriched cyclic β-amino alcohols, trans-2-aminocyclohexanols (ee, > 99%), trans 2-aminocylopentanols, trans 1amino-2indanols and trans 2amino 1-indanol were obtained via an Arthrobacter sp.
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