## Abstract The enantiomers of 1βmethylβ3β(10__H__βphenothiazineβ10βylmethyl)β1βazoniabicyclo[2,2,2]octane iodide (1) were prepared by chiral chromatographic resolution of the precursor mequitazine (2). The (+)β(S)βenantiomer 1b is 10βfold more potent than (β)β(R)βenantiomer 1a as a histamine antag
β¦ LIBER β¦
Syntheses and Determination of Absolute Configurations and Biological Activities of the Enantiomers of the Longtailed Mealybug Pheromone
β Scribed by Ramesh, Remya; Swaroop, Pandrangi Siva; Gonnade, Rajesh G.; Thirupathi, Choppari; Waterworth, Rebeccah A.; Millar, Jocelyn G.; Reddy, D. Srinivasa
- Book ID
- 120393291
- Publisher
- American Chemical Society
- Year
- 2013
- Tongue
- English
- Weight
- 545 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0022-3263
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