Springer Nature
Monatshefte fur Chemie
,  том 134 ,  издание 9 ,  страницы 1221-1227

Synthesis of Highly Functionalized Cyclobutene Derivatives

Тип публикации: Journal Article
Дата публикации: 2003-09-01
Springer Nature
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SJR: 0.341
CiteScore: 3.6
Impact factor: 2.2
ISSN: 00269247, 14344475
General Chemistry
Краткое описание
 Protonation of the reactive 1:1 intermediates produced in the reaction between triphenylphosphine and dialkyl acetylenedicarboxylates with CH-acids, such as ethyl 2,4-dioxo-hexanoate and ethyl 2,4-dioxo-5-methylhexanoate, lead to vinyltriphenylphosphonium salts, which undergo an intramolecular Wittig reaction to produce cyclobutene derivatives in fairly high yields.
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ГОСТ Скопировать
YAVARI I., Bayat M. Synthesis of Highly Functionalized Cyclobutene Derivatives // Monatshefte fur Chemie. 2003. Vol. 134. No. 9. pp. 1221-1227.
ГОСТ со всеми авторами (до 50) Скопировать
YAVARI I., Bayat M. Synthesis of Highly Functionalized Cyclobutene Derivatives // Monatshefte fur Chemie. 2003. Vol. 134. No. 9. pp. 1221-1227.
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TY - JOUR
DO - 10.1007/s00706-002-0609-1
UR - https://doi.org/10.1007/s00706-002-0609-1
TI - Synthesis of Highly Functionalized Cyclobutene Derivatives
T2 - Monatshefte fur Chemie
AU - YAVARI, ISSA
AU - Bayat, Mohammad
PY - 2003
DA - 2003/09/01
PB - Springer Nature
SP - 1221-1227
IS - 9
VL - 134
SN - 0026-9247
SN - 1434-4475
ER -
BibTex |
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@article{2003_YAVARI,
author = {ISSA YAVARI and Mohammad Bayat},
title = {Synthesis of Highly Functionalized Cyclobutene Derivatives},
journal = {Monatshefte fur Chemie},
year = {2003},
volume = {134},
publisher = {Springer Nature},
month = {sep},
url = {https://doi.org/10.1007/s00706-002-0609-1},
number = {9},
pages = {1221--1227},
doi = {10.1007/s00706-002-0609-1}
}
MLA
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MLA Скопировать
YAVARI, ISSA, and Mohammad Bayat. “Synthesis of Highly Functionalized Cyclobutene Derivatives.” Monatshefte fur Chemie, vol. 134, no. 9, Sep. 2003, pp. 1221-1227. https://doi.org/10.1007/s00706-002-0609-1.
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