Absolute configuration ofcis-5,6-dihydrodiol enantiomers derived from helical conformers of 1,12-dimethylbenz[a]anthracene
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry
Reference7 articles.
1. An X-ray determination of the crystal structures of 1,12-dimethylbenz[a]anthracene
2. Circular Dichroic Spectroscopy. Exciton Coupling in Organic Stereochemistry. Mill Valley, CA: University Science Books, 1983.
3. Absolute configurations of enantiomeric K-region cis-5,6-dihydrodiols of 12-methylbenz[A] anthracene and 7-bromo-12-methylbenz[A] anthracene
4. Elution order—absolute configuration relationship of k-region dinhydrodiol enantiomers of benz[a]anthracene derivatives in chiral stationary phase high-performance liquid chromatography
5. Direct enantiomeric resolution of some 7,12-dimethylbenz[a]anthracene derivatives by high-performance liquid chromatography with ionically and covalently bonded chiral stationary phases
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Regio- and Stereoselective Metabolism of 7,12-Dimethylbenz[ a ]anthracene by Mycobacterium vanbaalenii PYR-1;Applied and Environmental Microbiology;2003-07
2. Ultrafast semiinsulating InP:Fe-InGaAs:Fe-InP:Fe MSM photodetectors: modeling and performance;IEEE Journal of Quantum Electronics;1992
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