Springer Nature
Russian Chemical Bulletin
,  том 57 ,  издание 12 ,  страницы 2564-2571

8-Methoxy-5-methyl-2,3-dihydro-1H-cyclopenta[a]naphthalene: Synthesis and reactivity

Тип публикации: Journal Article
Дата публикации: 2008-12-01
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SJR: 0.305
CiteScore: 2.8
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ISSN: 10665285, 15739171
General Chemistry
Краткое описание
A new single-step approach to cyclopenta[a]naphthalenes through TiCl4-catalyzed reactions of 1-trimethylsilyloxycyclopentene with arylacetaldehydes was proposed. 8-Methoxy-5-methyl-2,3-dihydro-1H-cyclopenta[a]naphthalene and its derivatives were studied in oxidation and bromination reactions, as well as in hydrolytic cleavage of the O-Me bond.
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Asachenko A. F. et al. 8-Methoxy-5-methyl-2,3-dihydro-1H-cyclopenta[a]naphthalene: Synthesis and reactivity // Russian Chemical Bulletin. 2008. Vol. 57. No. 12. pp. 2564-2571.
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Asachenko A. F., Izmer V. V., Babkin A., Beletskaya I. P., Voskoboynikov A. Z. 8-Methoxy-5-methyl-2,3-dihydro-1H-cyclopenta[a]naphthalene: Synthesis and reactivity // Russian Chemical Bulletin. 2008. Vol. 57. No. 12. pp. 2564-2571.
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TY - JOUR
DO - 10.1007/s11172-008-0369-0
UR - https://doi.org/10.1007/s11172-008-0369-0
TI - 8-Methoxy-5-methyl-2,3-dihydro-1H-cyclopenta[a]naphthalene: Synthesis and reactivity
T2 - Russian Chemical Bulletin
AU - Asachenko, A F
AU - Izmer, V V
AU - Babkin, A.V.
AU - Beletskaya, I P
AU - Voskoboynikov, A Z
PY - 2008
DA - 2008/12/01
PB - Springer Nature
SP - 2564-2571
IS - 12
VL - 57
SN - 1066-5285
SN - 1573-9171
ER -
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@article{2008_Asachenko,
author = {A F Asachenko and V V Izmer and A.V. Babkin and I P Beletskaya and A Z Voskoboynikov},
title = {8-Methoxy-5-methyl-2,3-dihydro-1H-cyclopenta[a]naphthalene: Synthesis and reactivity},
journal = {Russian Chemical Bulletin},
year = {2008},
volume = {57},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007/s11172-008-0369-0},
number = {12},
pages = {2564--2571},
doi = {10.1007/s11172-008-0369-0}
}
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Asachenko, A. F., et al. “8-Methoxy-5-methyl-2,3-dihydro-1H-cyclopenta[a]naphthalene: Synthesis and reactivity.” Russian Chemical Bulletin, vol. 57, no. 12, Dec. 2008, pp. 2564-2571. https://doi.org/10.1007/s11172-008-0369-0.