volume 43 issue 5 pages 859-872

Syntheses with sulfones XLVII : stereoselective access to 1,3- and 1,4-dienes through hydrogenolysis of benzenesulfonyldienes. Application to pheromone synthesis

T Cuvigny 1
C Hervé Du Penhoat 1
M Julia 1
1
 
Ecole Normale Superieure, Laboratoire de Chimie, 24, rue Lhomond, 75231 Paris Cedex 05- France
Publication typeJournal Article
Publication date1987-01-01
scimago Q3
wos Q2
SJR0.426
CiteScore4.1
Impact factor2.2
ISSN00404020, 14645416
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
The stereospecific reduction of EE 2-benzenesulfonyl-1,3-dienes to ZE 1,3-dienes with Grignard reagents under transition metal catalysis ie described, Hydrogenolysis of the sulfonyl moiety of 2-benzenesulfonyl-1,4-dienes to ZE 1,4-dienes with sodium dithionite ie reported. These techniques have been applied to the stereoselective synthesis of (7E, 9Z) dodecadienyl acetate 3d , (9Z, 11E)tetradecadienyl acetate 3e and (9Z, 12E) tetradeoadienyl acetate, 6b .
Found 
Found 

Top-30

Journals

1
2
3
Tetrahedron Letters
3 publications, 10.71%
Tetrahedron
2 publications, 7.14%
Advanced Synthesis and Catalysis
2 publications, 7.14%
Synthetic Communications
2 publications, 7.14%
Russian Chemical Bulletin
1 publication, 3.57%
Journal of Organometallic Chemistry
1 publication, 3.57%
ChemInform
1 publication, 3.57%
Chemical Communications
1 publication, 3.57%
Organic and Biomolecular Chemistry
1 publication, 3.57%
Organic Chemistry Frontiers
1 publication, 3.57%
Palladium in Heterocyclic Chemistry - A Guide for the Synthetic Chemist
1 publication, 3.57%
Total Synthesis of Natural Products
1 publication, 3.57%
Russian Chemical Reviews
1 publication, 3.57%
1
2
3

Publishers

2
4
6
8
10
12
14
Elsevier
14 publications, 50%
Wiley
4 publications, 14.29%
Royal Society of Chemistry (RSC)
3 publications, 10.71%
Taylor & Francis
2 publications, 7.14%
Springer Nature
1 publication, 3.57%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 3.57%
2
4
6
8
10
12
14
  • We do not take into account publications without a DOI.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
28
Share
Cite this
GOST |
Cite this
GOST Copy
Cuvigny T., Du Penhoat C. H., Julia M. Syntheses with sulfones XLVII : stereoselective access to 1,3- and 1,4-dienes through hydrogenolysis of benzenesulfonyldienes. Application to pheromone synthesis // Tetrahedron. 1987. Vol. 43. No. 5. pp. 859-872.
GOST all authors (up to 50) Copy
Cuvigny T., Du Penhoat C. H., Julia M. Syntheses with sulfones XLVII : stereoselective access to 1,3- and 1,4-dienes through hydrogenolysis of benzenesulfonyldienes. Application to pheromone synthesis // Tetrahedron. 1987. Vol. 43. No. 5. pp. 859-872.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/s0040-4020(01)90023-7
UR - https://doi.org/10.1016/s0040-4020(01)90023-7
TI - Syntheses with sulfones XLVII : stereoselective access to 1,3- and 1,4-dienes through hydrogenolysis of benzenesulfonyldienes. Application to pheromone synthesis
T2 - Tetrahedron
AU - Cuvigny, T
AU - Du Penhoat, C Hervé
AU - Julia, M
PY - 1987
DA - 1987/01/01
PB - Elsevier
SP - 859-872
IS - 5
VL - 43
SN - 0040-4020
SN - 1464-5416
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{1987_Cuvigny,
author = {T Cuvigny and C Hervé Du Penhoat and M Julia},
title = {Syntheses with sulfones XLVII : stereoselective access to 1,3- and 1,4-dienes through hydrogenolysis of benzenesulfonyldienes. Application to pheromone synthesis},
journal = {Tetrahedron},
year = {1987},
volume = {43},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016/s0040-4020(01)90023-7},
number = {5},
pages = {859--872},
doi = {10.1016/s0040-4020(01)90023-7}
}
MLA
Cite this
MLA Copy
Cuvigny, T., et al. “Syntheses with sulfones XLVII : stereoselective access to 1,3- and 1,4-dienes through hydrogenolysis of benzenesulfonyldienes. Application to pheromone synthesis.” Tetrahedron, vol. 43, no. 5, Jan. 1987, pp. 859-872. https://doi.org/10.1016/s0040-4020(01)90023-7.