том 114 издание 26 страницы 10203-10213

Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives

Тип публикацииJournal Article
Дата публикации1992-12-01
scimago Q1
wos Q1
БС1
SJR5.489
CiteScore24.4
Impact factor15.6
ISSN00027863, 15205126
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Краткое описание
The absolute configuration of the stereogenic carbinol centers in nine annonaceous acetogenins has been determined by careful 1 H- and 19 F-NMR analysis of (S)- and (R)-Mosher ester [methoxy(trifluoromethyl)phenylacetate or MTPA] derivatives. These acetogenins include five adjacent bis-tetrahydrofuran acetogenins [uvaricin (3), bullatacin (4), bullatacinone (5), asimicin (6), and rolliniastatin 1 (7)] and four mono-tetrahydrofuran acetogenins [reticulatacin (8), isoannonacin-10-one (9), annonacin-10-one (10), and annonacin (11)]
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ГОСТ |
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Rieser M. J. et al. Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives // Journal of the American Chemical Society. 1992. Vol. 114. No. 26. pp. 10203-10213.
ГОСТ со всеми авторами (до 50) Скопировать
Rieser M. J., Hui Y., Rupprecht J. K., Kozlowski J. F., Wood K. V., MCLAUGHLIN J. L., Hanson P. R., Zhuang Z., Hoye T. R. Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives // Journal of the American Chemical Society. 1992. Vol. 114. No. 26. pp. 10203-10213.
RIS |
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TY - JOUR
DO - 10.1021/ja00052a018
UR - https://doi.org/10.1021/ja00052a018
TI - Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives
T2 - Journal of the American Chemical Society
AU - Rieser, Matthew J
AU - Hui, Yu-Hua
AU - Rupprecht, J Kent
AU - Kozlowski, John F
AU - Wood, Karl V.
AU - MCLAUGHLIN, Jerry L.
AU - Hanson, Paul R.
AU - Zhuang, Zhiping
AU - Hoye, Thomas R
PY - 1992
DA - 1992/12/01
PB - American Chemical Society (ACS)
SP - 10203-10213
IS - 26
VL - 114
SN - 0002-7863
SN - 1520-5126
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{1992_Rieser,
author = {Matthew J Rieser and Yu-Hua Hui and J Kent Rupprecht and John F Kozlowski and Karl V. Wood and Jerry L. MCLAUGHLIN and Paul R. Hanson and Zhiping Zhuang and Thomas R Hoye},
title = {Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives},
journal = {Journal of the American Chemical Society},
year = {1992},
volume = {114},
publisher = {American Chemical Society (ACS)},
month = {dec},
url = {https://doi.org/10.1021/ja00052a018},
number = {26},
pages = {10203--10213},
doi = {10.1021/ja00052a018}
}
MLA
Цитировать
Rieser, Matthew J., et al. “Determination of absolute configuration of stereogenic carbinol centers in annonaceous acetogenins by proton and fluorine 19-NMR analysis of Mosher ester derivatives.” Journal of the American Chemical Society, vol. 114, no. 26, Dec. 1992, pp. 10203-10213. https://doi.org/10.1021/ja00052a018.