Total synthesis of (−)-conocarpan and assignment of the absolute configuration by chemical methods
Publication type: Journal Article
Publication date: 2007-05-10
scimago Q1
wos Q2
SJR: 1.037
CiteScore: 7.4
Impact factor: 4.2
ISSN: 13597345, 1364548X
DOI:
10.1039/b704211f
PubMed ID:
17520119
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Abstract
(-)-Conocarpan (1) was synthesized by a method based on radical cyclization, and the absolute configuration was established by chemical degradation; the original 2R,3R-assignment to (+)-conocarpan should be reversed, as suggested by a later chiroptical study of model 2,3-dihydrobenzofurans.
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14
Total citations:
14
Citations from 2024:
0
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GOST
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Clive D. L., Stoffman E. J. Total synthesis of (−)-conocarpan and assignment of the absolute configuration by chemical methods // Chemical Communications. 2007. Vol. 21. pp. 2151-2153.
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Clive D. L., Stoffman E. J. Total synthesis of (−)-conocarpan and assignment of the absolute configuration by chemical methods // Chemical Communications. 2007. Vol. 21. pp. 2151-2153.
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RIS
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TY - JOUR
DO - 10.1039/b704211f
UR - https://doi.org/10.1039/b704211f
TI - Total synthesis of (−)-conocarpan and assignment of the absolute configuration by chemical methods
T2 - Chemical Communications
AU - Clive, Derrick L.J
AU - Stoffman, Elia J.L.
PY - 2007
DA - 2007/05/10
PB - Royal Society of Chemistry (RSC)
SP - 2151-2153
IS - 21
PMID - 17520119
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex (up to 50 authors)
Copy
@article{2007_Clive,
author = {Derrick L.J Clive and Elia J.L. Stoffman},
title = {Total synthesis of (−)-conocarpan and assignment of the absolute configuration by chemical methods},
journal = {Chemical Communications},
year = {2007},
publisher = {Royal Society of Chemistry (RSC)},
month = {may},
url = {https://doi.org/10.1039/b704211f},
number = {21},
pages = {2151--2153},
doi = {10.1039/b704211f}
}