Detailed Information on Publication Record
2002
Isoquinoline alkaloids: a 15N NMR and x-ray study. Part 2
MAREK, Radek, Jaromír MAREK, Jiří DOSTÁL, Eva TÁBORSKÁ, Jiří SLAVÍK et. al.Basic information
Original name
Isoquinoline alkaloids: a 15N NMR and x-ray study. Part 2
Authors
MAREK, Radek (203 Czech Republic, guarantor), Jaromír MAREK (203 Czech Republic), Jiří DOSTÁL (203 Czech Republic), Eva TÁBORSKÁ (203 Czech Republic), Jiří SLAVÍK (203 Czech Republic) and Roger DOMMISSE (56 Belgium)
Edition
Magnetic Resonance in Chemistry, West Sussex, John Wiley & Sons, Ltd. 2002, 0749-1581
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10401 Organic chemistry
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 0.994
RIV identification code
RIV/00216224:14310/02:00006431
Organization unit
Faculty of Science
UT WoS
000178816300002
Keywords in English
alkaloid; isoquinoline; 15N NMR; X-ray
Tags
Změněno: 22/6/2009 12:56, doc. RNDr. Jiří Dostál, CSc.
Abstract
V originále
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.
Links
| LN00A016, research and development project |
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