volume 39 issue 20 pages 3229-3232

The Heck olefination reaction; A DFT study of the elimination pathway

Publication typeJournal Article
Publication date1998-05-01
scimago Q3
wos Q3
SJR0.334
CiteScore3.2
Impact factor1.5
ISSN00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
Abstract Theoretical studies of the pathway in the Heck reaction between ethene and a methyl electrophile at [Pd(H2ACH2AH2)(CH3)(H2CCH2)]+ (A = P, N) reveal intermediates with an agostic H which is the one preferentially transferred to base.
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GOST |
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GOST Copy
Deeth R. J. et al. The Heck olefination reaction; A DFT study of the elimination pathway // Tetrahedron Letters. 1998. Vol. 39. No. 20. pp. 3229-3232.
GOST all authors (up to 50) Copy
Deeth R. J., Smith A., Hii K. K., John S. Brown (2) J. H. The Heck olefination reaction; A DFT study of the elimination pathway // Tetrahedron Letters. 1998. Vol. 39. No. 20. pp. 3229-3232.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/S0040-4039(98)00398-0
UR - https://doi.org/10.1016/S0040-4039(98)00398-0
TI - The Heck olefination reaction; A DFT study of the elimination pathway
T2 - Tetrahedron Letters
AU - Deeth, Robert J.
AU - Smith, Andrew
AU - Hii, King K.
AU - John S. Brown (2), John H.
PY - 1998
DA - 1998/05/01
PB - Elsevier
SP - 3229-3232
IS - 20
VL - 39
SN - 0040-4039
SN - 1873-3581
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{1998_Deeth,
author = {Robert J. Deeth and Andrew Smith and King K. Hii and John H. John S. Brown (2)},
title = {The Heck olefination reaction; A DFT study of the elimination pathway},
journal = {Tetrahedron Letters},
year = {1998},
volume = {39},
publisher = {Elsevier},
month = {may},
url = {https://doi.org/10.1016/S0040-4039(98)00398-0},
number = {20},
pages = {3229--3232},
doi = {10.1016/S0040-4039(98)00398-0}
}
MLA
Cite this
MLA Copy
Deeth, Robert J., et al. “The Heck olefination reaction; A DFT study of the elimination pathway.” Tetrahedron Letters, vol. 39, no. 20, May. 1998, pp. 3229-3232. https://doi.org/10.1016/S0040-4039(98)00398-0.