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Stereocontrol of 2-pyridone [4 + 4] photocycloaddition : a thermal-photochemical cycle to produce exclusively trans cycloadducts

Author
SIEBURGH, S. M; CHAO-HSIUNG LIN
State univ. New York Stony Brook, dep. chemistry, Stony Brook NY 11794-3400, United States
Source

Journal of organic chemistry. 1994, Vol 59, Num 13, pp 3597-3599

CODEN
JOCEAH
ISSN
0022-3263
Scientific domain
Biochemistry, molecular biology, biophysics; Organic chemistry
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Composé tétracyclique Cycle 6 chaînons Hétérocycle azote Lactame Photoaddition Réaction intramoléculaire Réaction photochimique Réaction thermique Stéréoisomère trans Stéréosélectivité Transposition Cope 3,6p-Triméthylènedipyridin-2-one(1,1p-diméthyl-1,1p,2,2p-tétrahydro) 3,9a:4,6a-Diéthénocyclopenta[b]-1,5-diazocine dérivé
Keyword (en)
Tetracyclic compound Six membered ring Nitrogen heterocycle Lactam Photoaddition Intramolecular reaction Photochemical reaction Thermal reaction Trans stereoisomer Stereoselectivity Cope rearrangement
Keyword (es)
Compuesto tetracíclico Ciclo 6 eslabones Heterociclo nitrógeno Lactamo Fotoadición Reacción intramolecular Reacción fotoquímica Reacción térmica Estereoisómero trans Estereoselectividad Transposición Cope
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4130362

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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