том 11 издание 13 страницы 2856-2859

Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides

Тип публикацииJournal Article
Дата публикации2009-06-09
scimago Q1
wos Q1
white level БС1
SJR1.235
CiteScore8.7
Impact factor5
ISSN15237060, 15237052
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
A triazolinylidene carbene catalyzed intermolecular Stetter reaction of glyoxamide and alkylidene ketoamides has been developed. 1,4-Dicarbonyl products are afforded in good to excellent yields, enantioselectivities, and diastereoselectivities. Further derivatization of the products affords useful intermediates for organic synthesis.
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ГОСТ |
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Liu Q., Rovis T. Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides // Organic Letters. 2009. Vol. 11. No. 13. pp. 2856-2859.
ГОСТ со всеми авторами (до 50) Скопировать
Liu Q., Rovis T. Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides // Organic Letters. 2009. Vol. 11. No. 13. pp. 2856-2859.
RIS |
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TY - JOUR
DO - 10.1021/ol901081a
UR - https://doi.org/10.1021/ol901081a
TI - Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides
T2 - Organic Letters
AU - Liu, Qin
AU - Rovis, Tomislav
PY - 2009
DA - 2009/06/09
PB - American Chemical Society (ACS)
SP - 2856-2859
IS - 13
VL - 11
PMID - 19507841
SN - 1523-7060
SN - 1523-7052
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2009_Liu,
author = {Qin Liu and Tomislav Rovis},
title = {Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides},
journal = {Organic Letters},
year = {2009},
volume = {11},
publisher = {American Chemical Society (ACS)},
month = {jun},
url = {https://doi.org/10.1021/ol901081a},
number = {13},
pages = {2856--2859},
doi = {10.1021/ol901081a}
}
MLA
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Liu, Qin, and Tomislav Rovis. “Enantio- and Diastereoselective Intermolecular Stetter Reaction of Glyoxamide and Alkylidene Ketoamides.” Organic Letters, vol. 11, no. 13, Jun. 2009, pp. 2856-2859. https://doi.org/10.1021/ol901081a.
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