Enantioselective Synthesis of Both Enantiomers of Cathinone via the Microbiological Reduction of 2-Azido-1-phenyl-1-propanone
β Scribed by Besse, Pascale; Veschambre, Henri; Dickman, Michael; Chenevert, Robert
- Book ID
- 117993454
- Publisher
- American Chemical Society
- Year
- 1994
- Tongue
- English
- Weight
- 506 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0022-3263
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π SIMILAR VOLUMES
Asymmetric Synthesis of Both Enantiomers of 2-(Dimethylamino)-1-[3-methoxy-2-(1-methylethoxy)phenyl]ethanol. -The synthesis of both enantiomers of the title compound (IX) based on the Sharpless asymmetric dihydroxylation of the vinylbenzene (IV) is described. Evaluation of their in vitro uroselecti
hbama:. A new facile ffmlz~ of pyrrolo [2,l-c][l,4]bonzodazepne (PBD) ring system has been achieved by reductive cyclization of the azide ~naploying hexamethyldligilathiarlΒ’ (HMDST). pment mmul~ituted PBD and the natunfl product DC-81 have also been prepmed in good overall yields