The stereochemistry and absolute configuration of narcotine
β Scribed by A.R. Battersby; H. Spencer
- Publisher
- Elsevier Science
- Year
- 1964
- Tongue
- French
- Weight
- 112 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
In the previous paper, we reported the stereochemistry of coronatine 1) , in which amino acid part, (+) -coronamic acid, was described as the enantiomer ofA on the basis of application of sector rule. 3) In this communication, we would like to describe further investigation on the stereochemistry of
DiTialon of chemioal PhJmfom, chomloal Xemewh Laborrtorieo, c.a.m.o., BOX 60 p.o., myton, vi0t0e, htrilia.
## Abstract For Abstract see ChemInform Abstract in Full Text.
The CD exciton chirality method was applied to determine the absolute stereochemistry of the strevertenes, antifungal pentaene macrolides produced by Streptoverticillium sp. LL-30F848. The CD difference spectrum of strevertene A methyl ester 15-dimethylaminobenzoate showed a positive couplet between