O-17 NMR-SPECTROSCOPY - GEOMETRIC EFFECTS ON INTRAMOLECULAR HYDROGEN-BONDING IN RIGID CARBONYL SYSTEMS

被引：13

作者：

BAUMSTARK, AL ^{[1
]}

GRAHAM, SS ^{[1
]}

BOYKIN, DW ^{[1
]}

机构：

[1] GEORGIA STATE UNIV,MICROBIOL & BIOCHEM SCI LAB,ATLANTA,GA 30303

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 07期

关键词：

D O I：

10.1016/S0040-4039(00)94402-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

17O NMR data for the carbonyl groups of a series of intramolecular hydrogen-bonded fluorenones and anthraquinones showed dependency on hydrogen bond angle and distance as well as relative acidity of NH donors. © 1990.

引用

页码：957 / 960

页数：4

共 16 条

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[3]

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[4]

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[5]

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[6] O-17 NMR-STUDIES OF TORSION ANGLE RELATIONSHIPS IN ARYL ALKYL KETONES AND AROMATIC-ALDEHYDES [J].

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[7] O-17 NMR-SPECTROSCOPY - ASSESSMENT OF STERIC PERTURBATION OF STRUCTURE IN ORGANIC-COMPOUNDS [J].

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[8] ABINITIO MO CALCULATIONS AND O-17 NMR AT NATURAL ABUNDANCE OF PARA-SUBSTITUTED ACETOPHENONES [J].

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[9]

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[10]

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