Výsledky vyhledávání - "Jan Dalmolen"

Diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide

Autor: Quirinus B. Broxterman, Jan Dalmolen, B. De Lange, Michiel van der Sluis, Richard M. Kellogg, QB Broxterman, B Kaptein

Publikováno v: Organic letters, 3(24), 3943-3946. AMER CHEMICAL SOC INC

[GRAPHICS]The highly diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide is reported. Homoallylamines with high enantiomeric purity are obtained from the adducts in three steps on removal of the chiral auxi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d7e3d458bd845120a974ffdf95057df
https://doi.org/10.1021/ol016840f

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Accurate quantitation of pentaerythritol tetranitrate and its degradation products using liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry

Autor: Peter J. Schoenmakers, Hanneke Brust, Arian C. van Asten, Antoine E. D. M. van der Heijden, Jan Dalmolen, Mattijs Koeberg

Publikováno v: Journal of Chromatography A, 1338, 111-116
Journal of Chromatography A, 1338, 111-116. Elsevier

After an explosion of pentaerythritol tetranitrate (PETN), its degradation products pentaerythritol trinitrate (PETriN), dinitrate (PEDiN) and mononitrate (PEMN) were detected using liquid chromatography-atmospheric-pressure chemical-ionization-mass

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc9ccc60f591945258472821c7f26bea
https://pubmed.ncbi.nlm.nih.gov/24656542

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ChemInform Abstract: Diastereoselective Addition of Allylzinc Bromide to Imines Derived from (R)-Phenylglycine Amide

Autor: Quirinus B. Broxterman, Bernard Kaptein, Richard M. Kellogg, Jan Dalmolen, Ben De Lange, Marcel van der Sluis

Publikováno v: ChemInform. 33

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b8ec0b446c86d90532b36367ff918ad1
https://doi.org/10.1002/chin.200217026

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Synthesis of Enantiopure 1-Aryl-1-butylamines and 1-Aryl-3-butenylamines by Diastereoselective Addition of Allylzinc Bromide to Imines Derived from (R)-Phenylglycine Amide

Autor: Marcel van der Sluis, Ben de Lange, José W. Nieuwenhuijzen, Quirinus B. Broxterman, Auke Meetsma, Jan Dalmolen, Bernard Kaptein, Richard M. Kellogg

Publikováno v: European Journal of Organic Chemistry, 35(32), 1544-1557. WILEY-V C H VERLAG GMBH

The synthesis of enantiopure 1-aryl-1-butylamines via a highly diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide is reported. These are synthesised by a three-step procedure, which involves: (a) formation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77008a33de5b6dbbcc5e5a9a4b17a6f8
https://doi.org/10.1002/chin.200432084

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Akademický článek

The Dutch Resolution Variant of the Classical Resolution of Racemates by Formation of Diastereomeric Salts: Family Behaviour in Nucleation Inhibition.

Autor: Jan Dalmolen, Theodora D. Tiemersma-Wegman, José W. Nieuwenhuijzen, Marcel van der Sluis, Erik van Echten, Ton R. Vries, Bernard Kaptein, Quirinius B. Broxterman, Richard M. Kellogg

Publikováno v: Chemistry - A European Journal; Sep2005, Vol. 11 Issue 19, p5619-5624, 6p

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Akademický článek

Synthesis of Enantiopure 1-Aryl-1-butylamines and 1-Aryl-3-butenylamines by Diastereoselective Addition of Allylzinc Bromide to Imines Derived from (R)-Phenylglycine Amide.

Autor: Jan Dalmolen, Marcel van der Sluis, José W. Nieuwenhuijzen, Auke Meetsma, Ben de Lange, Bernard Kaptein, Richard M. Kellogg, Quirinus B. Broxterman

Publikováno v: European Journal of Organic Chemistry; Apr2004, Vol. 2004 Issue 7, p1544-1557, 14p

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