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Oxime formation of 4-epi-(acetylamino)-5-oxo-4-deoxy-avermectin B1

Author
CVETOVICH, R. J; LEONARD, W. R; AMATO, J. S; DIMICHELE, L. M; REAMER, R. A; SHUMAN, R. F; GRABOWSKI, E. J. J
Merck Research Laboratories, dep. process res., Division Merck & Co., Inc., Rahway NJ 07065, United States
Source

Journal of organic chemistry. 1994, Vol 59, Num 19, pp 5838-5840 ; ref : 11 ref

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)
Acide Lewis Acétal Alcool Catalyse acide Cétoxime Epimère Hydroxylamine Hétérocycle oxygène Lactone Macrocycle Spirane Zinc II Chlorure Avermectine B1(4s-acétamido-4s-désoxy) Hydroxylamine(O-triméthylsilyl) Phosphorodichloridate Propan-2-ol
Keyword (en)
Lewis acid Acetal Alcohol Acid catalysis Ketoxime Epimer Hydroxylamine Oxygen heterocycle Lactone Macrocycle Spiran Zinc II Chlorides
Keyword (es)
Acido Lewis Acetal Alcohol Catálisis ácida Cetoxima Epímero Hidroxilamina Heterociclo oxígeno Lactona Macrociclo Espirano Zinc II Cloruro
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4228040

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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