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Stereoselective synthesis of 2-aminocyclobutanols via photocyclization of α-amido alkylaryl ketones: Mechanistic implications for the Norrish/Yang reaction

Author
GRIESBECK, Axel G1 ; HECKROTH, Heike1
[1] Contribution from the Institute of Organic Chemistry, Greinstrasse 4, 50939 Köln, Germany
Source

Journal of the American Chemical Society. 2002, Vol 124, Num 3, pp 396-403

CODEN
JACSAT
ISSN
0002-7863
Scientific domain
Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Butyrophénone dérivé Composé benzénique Cyclisation Diastéréosélectivité Diradical libre organique Enlèvement hydrogène Etude expérimentale Intermédiaire réaction Liaison hydrogène intramoléculaire Rayonnement UV proche Réaction photochimique Solvant organique Spectrométrie RMN Transfert hydrogène Cyclobutanol dérivé Réaction Norrish Yang
Keyword (en)
Butyrophenone derivatives Benzenic compound Cyclization Diastereoselectivity Organic free biradical Hydrogen abstraction Experimental study Reaction intermediate Intramolecular hydrogen bond Near ultraviolet radiation Photochemical reaction Organic solvent NMR spectrometry Hydrogen transfer
Keyword (es)
Butirofenona derivado Compuesto bencénico Ciclización Diastereoselectividad Dirradical libre orgánico Abstracción hidrógeno Estudio experimental Intermediario reacción Enlace hidrógeno intramolecular Radiación ultravioleta próxima Reacción fotoquímica Solvente orgánico Espectrometría RMN Transferencia hidrógeno
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01F Physical chemistry of induced reactions (with radiations, particles and ultrasonics) / 001C01F01 Photochemistry

Discipline
General chemistry and physical chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
13517887

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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