Chemoselectivity and enantiocontrol in catalytic intramolecular metal carbene reactions of diazo acetates linked to reactive functional groups by naphthalene-1,8-dimethanol

Chemical Communications

Volumn , Issue 17, 1999, Pages 1691-1692

  Doyle, Michael P ^a   Ene, Doina G ^a   Forbes, David C ^a   Pillow, Thomas H ^a  

^a University of Arizona ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DIAZO ACETATE; DIAZONIUM COMPOUND; FUNCTIONAL GROUP; NAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; DRUG DECOMPOSITION; DRUG SELECTIVITY; DRUG STRUCTURE; DRUG TRANSFORMATION; ENANTIOMER;

EID: 0033533476     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a904530i     Document Type: Article

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14. Only one product was observed by GC and NMR analyses and, based on results reported in ref. 10, this product is assumed to be the erythro isomer.
15. 2: C, 78.77; H, 5.08. Found: C, 77.95; H, 5.14%).