Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol
Тип публикации: Journal Article
Дата публикации: 1988-04-01
scimago Q2
wos Q1
БС1
SJR: 0.737
CiteScore: 6.1
Impact factor: 3.6
ISSN: 00223263, 15206904
Organic Chemistry
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Heathcock C. H. et al. Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol // Journal of Organic Chemistry. 1988. Vol. 53. No. 9. pp. 1922-1942.
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Heathcock C. H., Finkelstein B. L., Jarvi E. T., Radel P. A., Hadley C. R. Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol // Journal of Organic Chemistry. 1988. Vol. 53. No. 9. pp. 1922-1942.
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TY - JOUR
DO - 10.1021/jo00244a017
UR - https://doi.org/10.1021/jo00244a017
TI - Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol
T2 - Journal of Organic Chemistry
AU - Heathcock, Clayton H.
AU - Finkelstein, Bruce L.
AU - Jarvi, Esa T
AU - Radel, Peggy A
AU - Hadley, Cheri R
PY - 1988
DA - 1988/04/01
PB - American Chemical Society (ACS)
SP - 1922-1942
IS - 9
VL - 53
SN - 0022-3263
SN - 1520-6904
ER -
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@article{1988_Heathcock,
author = {Clayton H. Heathcock and Bruce L. Finkelstein and Esa T Jarvi and Peggy A Radel and Cheri R Hadley},
title = {Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol},
journal = {Journal of Organic Chemistry},
year = {1988},
volume = {53},
publisher = {American Chemical Society (ACS)},
month = {apr},
url = {https://doi.org/10.1021/jo00244a017},
number = {9},
pages = {1922--1942},
doi = {10.1021/jo00244a017}
}
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MLA
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Heathcock, Clayton H., et al. “Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diol.” Journal of Organic Chemistry, vol. 53, no. 9, Apr. 1988, pp. 1922-1942. https://doi.org/10.1021/jo00244a017.