FTIR spectral study of intramolecular hydrogen bonding in E-type of 15-keto-prostaglandins in dilute CCl4 solution: Structure-activity relationships
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry
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1. Synthesis of thromboxane A2
2. Biosynthesis of 9α,15-Dihydroxy-11-ketoprost-13-enoic Acid
3. Biosynthesis and chemistry of 9α, 15(S)-dihydroxy-11-oxo-13-trans-prostenoic acid
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. Study of substituent effects on intramolecular hydrogen bonding of (5Z)-7-[(1R,2R,3S,5S)-2-(4-substituted benzoylamino)-6,6-dimethylbicyclo[3.1.1]hept-3-yl]hept-5-enoic acids and their esters in dilute CCl4 solution by FTIR spectroscopy;Vibrational Spectroscopy;2003-09
2. Study of substituent effects on rotational isomers and monomer–dimer equilibria of the 3-carboxy group in 4-substituted (R)-2-(3,4-methylenedioxyphenyl)-6-isopropyloxy-2H-chromen-3-carboxylic acids in dilute CCl4 and CHCl3 solutions by FTIR spectroscopy;Vibrational Spectroscopy;2001-02
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