том 10 издание 12 страницы 921-927

Routes to trans-Chrysanthemic Acid. I. Elaboration of (-)Dihydrochrysanthemclactone from (+)3-Carene

Тип публикацииJournal Article
Дата публикации1980-01-01
SCImago Q3
WOS Q3
БС2
SJR0.269
CiteScore3.5
Impact factor2
ISSN00397911, 15322432
Organic Chemistry
Краткое описание
A popular synthetic target usually embodies unique structural features and/or implicates practical use. Chrysanthemic acid (1) which meets both criteria has indeed attracted enormous effort in its synthesis.1 From a utilitarian viewpoint, the total synthesis of trans-chrysanthemic acid is attended by the drawback of requiring optical resolution,2 because only the dextrorotatory antipode proves valuable for reconstitution of pyrethroid insecticides.
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ГОСТ |
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Ho T., Din Z. Routes to trans-Chrysanthemic Acid. I. Elaboration of (-)Dihydrochrysanthemclactone from (+)3-Carene // Synthetic Communications. 1980. Vol. 10. No. 12. pp. 921-927.
ГОСТ со всеми авторами (до 50) Скопировать
Ho T., Din Z. Routes to trans-Chrysanthemic Acid. I. Elaboration of (-)Dihydrochrysanthemclactone from (+)3-Carene // Synthetic Communications. 1980. Vol. 10. No. 12. pp. 921-927.
RIS |
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TY - JOUR
DO - 10.1080/00397918008061852
UR - https://doi.org/10.1080/00397918008061852
TI - Routes to trans-Chrysanthemic Acid. I. Elaboration of (-)Dihydrochrysanthemclactone from (+)3-Carene
T2 - Synthetic Communications
AU - Ho, Tse-Lok
AU - Din, Zia-ud
PY - 1980
DA - 1980/01/01
PB - Taylor & Francis
SP - 921-927
IS - 12
VL - 10
SN - 0039-7911
SN - 1532-2432
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{1980_Ho,
author = {Tse-Lok Ho and Zia-ud Din},
title = {Routes to trans-Chrysanthemic Acid. I. Elaboration of (-)Dihydrochrysanthemclactone from (+)3-Carene},
journal = {Synthetic Communications},
year = {1980},
volume = {10},
publisher = {Taylor & Francis},
month = {jan},
url = {https://doi.org/10.1080/00397918008061852},
number = {12},
pages = {921--927},
doi = {10.1080/00397918008061852}
}
MLA
Цитировать
Ho, Tse-Lok, and Zia-ud Din. “Routes to trans-Chrysanthemic Acid. I. Elaboration of (-)Dihydrochrysanthemclactone from (+)3-Carene.” Synthetic Communications, vol. 10, no. 12, Jan. 1980, pp. 921-927. https://doi.org/10.1080/00397918008061852.
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