том 44 издание 13 страницы 2733-2736

A highly efficient olefin metathesis initiator: improved synthesis and reactivity studies

Тип публикацииJournal Article
Дата публикации2003-03-25
scimago Q3
wos Q3
БС2
SJR0.334
CiteScore3.2
Impact factor1.5
ISSN00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
The synthesis of ligand 8, required for the preparation of catalyst 4c has been optimised. Ligand exchange studies indicate that biphenyl-based alkylidene 4c initiates considerably faster than its unsubstituted analogue 4a. The performance of 4c in ring-opening cross metathesis reactions involving substrates containing unprotected chelating atoms is also reported.
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ГОСТ |
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Dunne A. M., Mix S., Blechert S. A highly efficient olefin metathesis initiator: improved synthesis and reactivity studies // Tetrahedron Letters. 2003. Vol. 44. No. 13. pp. 2733-2736.
ГОСТ со всеми авторами (до 50) Скопировать
Dunne A. M., Mix S., Blechert S. A highly efficient olefin metathesis initiator: improved synthesis and reactivity studies // Tetrahedron Letters. 2003. Vol. 44. No. 13. pp. 2733-2736.
RIS |
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TY - JOUR
DO - 10.1016/S0040-4039(03)00346-0
UR - https://doi.org/10.1016/S0040-4039(03)00346-0
TI - A highly efficient olefin metathesis initiator: improved synthesis and reactivity studies
T2 - Tetrahedron Letters
AU - Dunne, Aideen M
AU - Mix, Stefan
AU - Blechert, Siegfried
PY - 2003
DA - 2003/03/25
PB - Elsevier
SP - 2733-2736
IS - 13
VL - 44
SN - 0040-4039
SN - 1873-3581
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2003_Dunne,
author = {Aideen M Dunne and Stefan Mix and Siegfried Blechert},
title = {A highly efficient olefin metathesis initiator: improved synthesis and reactivity studies},
journal = {Tetrahedron Letters},
year = {2003},
volume = {44},
publisher = {Elsevier},
month = {mar},
url = {https://doi.org/10.1016/S0040-4039(03)00346-0},
number = {13},
pages = {2733--2736},
doi = {10.1016/S0040-4039(03)00346-0}
}
MLA
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Dunne, Aideen M., et al. “A highly efficient olefin metathesis initiator: improved synthesis and reactivity studies.” Tetrahedron Letters, vol. 44, no. 13, Mar. 2003, pp. 2733-2736. https://doi.org/10.1016/S0040-4039(03)00346-0.