Total Synthesis of 1-Oxomiltirone and Arucadiol
1
Department of Chemistry and Research Institute of Natural Science
2
Faculty of Chemistry
Publication type: Journal Article
Publication date: 2019-11-05
scimago Q3
wos Q3
SJR: 0.437
CiteScore: 3.3
Impact factor: 1.4
ISSN: 09365214, 14372096
Organic Chemistry
Abstract
A practical and efficient approach for the total synthesis of arucadiol and 1-oxomiltirone is reported. The key step which involves an intramolecular [4+2] cycloaddition catalyzed by gold(III) bromide or copper(II) triflate leads to the formation of 6-6-6-fused aromatic abietane core.
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Total citations:
9
Citations from 2024:
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GOST
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Oh C. H. et al. Total Synthesis of 1-Oxomiltirone and Arucadiol // Synlett. 2019. Vol. 31. No. 19. pp. 1953-1956.
GOST all authors (up to 50)
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Oh C. H., Seong C., Kang J., Chai U., Mac D. H. Total Synthesis of 1-Oxomiltirone and Arucadiol // Synlett. 2019. Vol. 31. No. 19. pp. 1953-1956.
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RIS
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TY - JOUR
DO - 10.1055/s-0039-1690743
UR - https://doi.org/10.1055/s-0039-1690743
TI - Total Synthesis of 1-Oxomiltirone and Arucadiol
T2 - Synlett
AU - Oh, Chang Ho
AU - Seong, Chaehyeon
AU - Kang, Juyeon
AU - Chai, Uiseong
AU - Mac, Dinh Hung
PY - 2019
DA - 2019/11/05
PB - Georg Thieme Verlag KG
SP - 1953-1956
IS - 19
VL - 31
SN - 0936-5214
SN - 1437-2096
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2019_Oh,
author = {Chang Ho Oh and Chaehyeon Seong and Juyeon Kang and Uiseong Chai and Dinh Hung Mac},
title = {Total Synthesis of 1-Oxomiltirone and Arucadiol},
journal = {Synlett},
year = {2019},
volume = {31},
publisher = {Georg Thieme Verlag KG},
month = {nov},
url = {https://doi.org/10.1055/s-0039-1690743},
number = {19},
pages = {1953--1956},
doi = {10.1055/s-0039-1690743}
}
Cite this
MLA
Copy
Oh, Chang Ho, et al. “Total Synthesis of 1-Oxomiltirone and Arucadiol.” Synlett, vol. 31, no. 19, Nov. 2019, pp. 1953-1956. https://doi.org/10.1055/s-0039-1690743.