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@article{405423,
author = {Marek, Radek and Marek, Jaromír and Dostál, Jiří and Táborská, Eva and Slavík, Jiří and Dommisse, Roger},
article_location = {West Sussex},
article_number = {11},
keywords = {alkaloid; isoquinoline; 15N NMR; X-ray},
language = {eng},
issn = {0749-1581},
journal = {Magnetic Resonance in Chemistry},
title = {Isoquinoline alkaloids: a 15N NMR and x-ray study. Part 2},
url = {http://www3.interscience.wiley.com/cgi-bin/abstract/98518855/START},
volume = {40},
year = {2002}
}
TY - JOUR
ID - 405423
AU - Marek, Radek - Marek, Jaromír - Dostál, Jiří - Táborská, Eva - Slavík, Jiří - Dommisse, Roger
PY - 2002
TI - Isoquinoline alkaloids: a 15N NMR and x-ray study. Part 2
JF - Magnetic Resonance in Chemistry
VL - 40
IS - 11
SP - 687
EP - 687
PB - John Wiley & Sons, Ltd.
SN - 07491581
KW - alkaloid
KW - isoquinoline
KW - 15N NMR
KW - X-ray
UR - http://www3.interscience.wiley.com/cgi-bin/abstract/98518855/START
N2 - Continuing our systematic 15N NMR study of isoquinoline alkaloids, we report a contribution extending our previous paper. The 15N NMR chemical shifts and 15N,1H long-range coupling pathways of tertiary and quaternary isoquinoline alkaloids of several constitutional types are presented. The selected compounds belong to the protoberberine, proaporphine, pavinane, rhoeadine and phtalideisoquinoline classes of alkaloids and were investigated by gradient-selected inverse-detected multiple bond correlation experiments (GHMBC and GSQMBC). In addition, x-ray data and the principal geometric parameters of stylopine, mecambridine, norchelerythrine, isothebaine and mecambrine are reported and discussed.
ER -
MAREK, Radek, Jaromír MAREK, Jiří DOSTÁL, Eva TÁBORSKÁ, Jiří SLAVÍK and Roger DOMMISSE. Isoquinoline alkaloids: a 15N NMR and x-ray study. Part 2. \textit{Magnetic Resonance in Chemistry}. West Sussex: John Wiley \&{} Sons, Ltd., 2002, vol.~40, No~11, p.~687-692. ISSN~0749-1581.
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