Synthesis and acylation of allylic mercuric iodides: a convenient synthesis of allylic ketones
Тип публикации: Journal Article
Дата публикации: 1993-05-01
scimago Q2
wos Q1
white level БС1
SJR: 0.737
CiteScore: 6.1
Impact factor: 3.6
ISSN: 00223263, 15206904
Organic Chemistry
Краткое описание
Allylic mercuric iodides are readily prepared by the reaction of mercury(0) and allylic iodides. They undergo efficient acylation with allylic rearrangement upon reaction with acyl chlorides and aluminum chloride to provide a convenient synthesis of allylic ketones. Artemisia ketone is prepared in two steps by this approach
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ГОСТ
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Larock R. C., Lu Y. D. Synthesis and acylation of allylic mercuric iodides: a convenient synthesis of allylic ketones // Journal of Organic Chemistry. 1993. Vol. 58. No. 10. pp. 2846-2850.
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Larock R. C., Lu Y. D. Synthesis and acylation of allylic mercuric iodides: a convenient synthesis of allylic ketones // Journal of Organic Chemistry. 1993. Vol. 58. No. 10. pp. 2846-2850.
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TY - JOUR
DO - 10.1021/jo00062a031
UR - https://doi.org/10.1021/jo00062a031
TI - Synthesis and acylation of allylic mercuric iodides: a convenient synthesis of allylic ketones
T2 - Journal of Organic Chemistry
AU - Larock, Richard C.
AU - Lu, Yong De
PY - 1993
DA - 1993/05/01
PB - American Chemical Society (ACS)
SP - 2846-2850
IS - 10
VL - 58
SN - 0022-3263
SN - 1520-6904
ER -
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BibTex (до 50 авторов)
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@article{1993_Larock,
author = {Richard C. Larock and Yong De Lu},
title = {Synthesis and acylation of allylic mercuric iodides: a convenient synthesis of allylic ketones},
journal = {Journal of Organic Chemistry},
year = {1993},
volume = {58},
publisher = {American Chemical Society (ACS)},
month = {may},
url = {https://doi.org/10.1021/jo00062a031},
number = {10},
pages = {2846--2850},
doi = {10.1021/jo00062a031}
}
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MLA
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Larock, Richard C., and Yong De Lu. “Synthesis and acylation of allylic mercuric iodides: a convenient synthesis of allylic ketones.” Journal of Organic Chemistry, vol. 58, no. 10, May. 1993, pp. 2846-2850. https://doi.org/10.1021/jo00062a031.
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