Total Synthesis of (−)-Reveromycin A
Publication type: Journal Article
Publication date: 2004-07-22
scimago Q1
wos Q1
SJR: 1.235
CiteScore: 8.7
Impact factor: 5.0
ISSN: 15237060, 15237052
PubMed ID:
15330668
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
The asymmetric total synthesis of (-)-reveromycin A is described. The key steps involved a Lewis acid catalyzed inverse electron demand hetero-Diels-Alder reaction followed by hydroboration/oxidation to afford the spiroketal core 4 in a highly stereoselective manner and introduction of the C18 hemisuccinate by high-pressure acylation.
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Metrics
29
Total citations:
29
Citations from 2024:
3
(10.35%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
El Sous M. et al. Total Synthesis of (−)-Reveromycin A // Organic Letters. 2004. Vol. 6. No. 17. pp. 3001-3004.
GOST all authors (up to 50)
Copy
El Sous M., Ganame D., Tregloan P. A., Rizzacasa M. A. Total Synthesis of (−)-Reveromycin A // Organic Letters. 2004. Vol. 6. No. 17. pp. 3001-3004.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/ol048811l
UR - https://doi.org/10.1021/ol048811l
TI - Total Synthesis of (−)-Reveromycin A
T2 - Organic Letters
AU - El Sous, Mariana
AU - Ganame, Danny
AU - Tregloan, Peter A.
AU - Rizzacasa, Mark A
PY - 2004
DA - 2004/07/22
PB - American Chemical Society (ACS)
SP - 3001-3004
IS - 17
VL - 6
PMID - 15330668
SN - 1523-7060
SN - 1523-7052
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2004_El Sous,
author = {Mariana El Sous and Danny Ganame and Peter A. Tregloan and Mark A Rizzacasa},
title = {Total Synthesis of (−)-Reveromycin A},
journal = {Organic Letters},
year = {2004},
volume = {6},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/ol048811l},
number = {17},
pages = {3001--3004},
doi = {10.1021/ol048811l}
}
Cite this
MLA
Copy
El Sous, Mariana, et al. “Total Synthesis of (−)-Reveromycin A.” Organic Letters, vol. 6, no. 17, Jul. 2004, pp. 3001-3004. https://doi.org/10.1021/ol048811l.