CONFORMATIONAL-ANALYSIS BY RING CURRENT METHOD - THE STRUCTURE OF 2,2,12,12-TETRAMETHYL[4.4]METACYCLOPHANE

被引：45
作者：
FUKAZAWA, Y
OGATA, K
USUI, S
机构：
来源：
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1988年 / 110卷 / 26期
关键词：
D O I：
10.1021/ja00234a018
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
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页码：8692 / 8693
页数：2
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共 37 条
[1]   RING CURRENTS, LOCAL ANISOTROPY, AND PROBLEM OF OUT-OF-PLANE PROTONS - REINVESTIGATION OF NUCLEAR MAGNETIC-RESONANCE SPECTRUM OF [10]-PARACYCLOPHANE [J].
AGARWAL, A ;
BARNES, JA ;
FLETCHER, JL ;
MCGLINCHEY, MJ ;
SAYER, BG .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1977, 55 (13) :2575-2581
[2]  
Allinger N. L., 1980, QCPE, P395
[3]   CONFORMATIONAL-ANALYSIS .130. MM2 - HYDROCARBON FORCE-FIELD UTILIZING V1 AND V2 TORSIONAL TERMS [J].
ALLINGER, NL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (25) :8127-8134
[4]   NUCLEAR MAGNETIC RESONANCE SPECTRAL ASSIGNMENTS FROM NUCLEAR OVERHAUSER EFFECTS [J].
ANET, FAL ;
BOURN, AJR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (22) :5250-&
[5]   CORRELATION OF INTRAMOLECULAR NUCLEAR OVERHAUSER EFFECT WITH INTERNUCLEAR DISTANCE [J].
BELL, RA ;
SAUNDERS, JK .
CANADIAN JOURNAL OF CHEMISTRY, 1970, 48 (07) :1114-&
[6]   THE CRYSTAL AND MOLECULAR-STRUCTURE OF 2,3,12,13-TETRATHIA[4,4]METACYCLOPHANE [J].
BEVERIDGE, KA ;
BUSHNELL, GW ;
MITCHELL, RH .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1983, 61 (07) :1603-1607
[7]  
Bovey F. A., 1969, NUCL MAGN RESON, P64
[8]   STEREOCHEMISTRY OF THE HYGROLIDINS [J].
COREY, EJ ;
PONDER, JW .
TETRAHEDRON LETTERS, 1984, 25 (39) :4325-4328
[9]   DYNAMIC STEREOCHEMISTRY OF 2,3,12,13-TETRATHIA-SELENA[4,4]METACYCLOPHANE AND 2,3,12,13-TETRASELENA[4,4]METACYCLOPHANE [J].
DIXON, KR ;
MITCHELL, RH .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1983, 61 (07) :1598-1602
[10]   CONFORMATIONAL STUDY OF THE CEMBRANOLIDE DITERPENE DENTICULATOLIDE BY MOLECULAR MECHANICS METHOD [J].
FUKAZAWA, Y ;
USUI, S ;
UCHIO, Y ;
SHIOBARA, Y ;
KODAMA, M .
TETRAHEDRON LETTERS, 1986, 27 (16) :1825-1828
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