1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride-mediated oxazole rearrangement: Gaining access to a unique marine alkaloid scaffold

Journal of Organic Chemistry

Volumn 74, Issue 9, 2009, Pages 3406-3413

  Hupp, Christopher D ^a   Tepe, Jetze J ^a  

^a MICHIGAN STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBODIIMIDE HYDROCHLORIDES; GAINING ACCESS; HYDANTOINS; MARINE ALKALOIDS; NATURAL PRODUCTS; OXAZOLE; QUATERNARY STEREOCENTER; STEREOCENTERS; STRUCTURAL DIVERSITY; SYNTHETIC UTILITY; TOTAL SYNTHESIS;

GARNETS;

SCAFFOLDS;

1 (3 DIMETHYLAMINOPROPYL) 3 ETHYLCARBODIIMIDE; 2 AMINO 5 (1H INDOL 3 YL) 5 (2 OXOPROPYL) 1H IMIDAZOL 4 (5H) ONE; 5 (1H INDOL 3 YL) 5 (2 OXOPROPYL)IMIDAZOLIDINE 2,4 DIONE; ALKALOID; OXAZOLE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; GROSSULARIACEAE; REACTION ANALYSIS;

ALKALOIDS; ANIMALS; BIOLOGICAL PRODUCTS; ETHYLDIMETHYLAMINOPROPYL CARBODIIMIDE; INDOLES; OCEANS AND SEAS; OXAZOLES; UROCHORDATA;

EID: 66449126274     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900264p     Document Type: Article

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