Enantioselective Synthesis of Spirobarbiturate-Cyclohexenes through Phosphine-Catalyzed Asymmetric [4 + 2] Annulation of Barbiturate-Derived Alkenes with Allenoates
Тип публикации: Journal Article
Дата публикации: 2016-03-03
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR: 1.007
CiteScore: 7.7
Impact factor: 4.7
ISSN: 15237060, 15237052
PubMed ID:
26937706
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
An enantioselective synthesis of pharmaceutically important spirobarbiturates has been achieved via spirocyclic chiral phosphine-catalyzed asymmetric [4 + 2] annulation of barbiturate-derived alkenes with allenoates. With the use of this tool, various spirobarbiturate-cyclohexenes are obtained in good to excellent yields with excellent diastereo- and enantioselectivities. A wide range of α-substituted allenoates and barbiturate-derived alkenes were tolerated.
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115
Всего цитирований:
115
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(15.66%)
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LIU H. et al. Enantioselective Synthesis of Spirobarbiturate-Cyclohexenes through Phosphine-Catalyzed Asymmetric [4 + 2] Annulation of Barbiturate-Derived Alkenes with Allenoates // Organic Letters. 2016. Vol. 18. No. 6. pp. 1302-1305.
ГОСТ со всеми авторами (до 50)
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LIU H., Liu Y., Yuan C., Wang G., Zhu S., Wu Y., Wang B., Sun Z., Xiao Y., Zhou Q., Guo H. Enantioselective Synthesis of Spirobarbiturate-Cyclohexenes through Phosphine-Catalyzed Asymmetric [4 + 2] Annulation of Barbiturate-Derived Alkenes with Allenoates // Organic Letters. 2016. Vol. 18. No. 6. pp. 1302-1305.
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TY - JOUR
DO - 10.1021/acs.orglett.6b00239
UR - https://doi.org/10.1021/acs.orglett.6b00239
TI - Enantioselective Synthesis of Spirobarbiturate-Cyclohexenes through Phosphine-Catalyzed Asymmetric [4 + 2] Annulation of Barbiturate-Derived Alkenes with Allenoates
T2 - Organic Letters
AU - LIU, HONGLEI
AU - Liu, Yang
AU - Yuan, Chunhao
AU - Wang, Guo-Peng
AU - Zhu, Shoufei
AU - Wu, Yang
AU - Wang, Bo
AU - Sun, Zhanhu
AU - Xiao, Yumei
AU - Zhou, Qilin
AU - Guo, Hongchao
PY - 2016
DA - 2016/03/03
PB - American Chemical Society (ACS)
SP - 1302-1305
IS - 6
VL - 18
PMID - 26937706
SN - 1523-7060
SN - 1523-7052
ER -
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BibTex (до 50 авторов)
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@article{2016_LIU,
author = {HONGLEI LIU and Yang Liu and Chunhao Yuan and Guo-Peng Wang and Shoufei Zhu and Yang Wu and Bo Wang and Zhanhu Sun and Yumei Xiao and Qilin Zhou and Hongchao Guo},
title = {Enantioselective Synthesis of Spirobarbiturate-Cyclohexenes through Phosphine-Catalyzed Asymmetric [4 + 2] Annulation of Barbiturate-Derived Alkenes with Allenoates},
journal = {Organic Letters},
year = {2016},
volume = {18},
publisher = {American Chemical Society (ACS)},
month = {mar},
url = {https://doi.org/10.1021/acs.orglett.6b00239},
number = {6},
pages = {1302--1305},
doi = {10.1021/acs.orglett.6b00239}
}
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MLA
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LIU, HONGLEI, et al. “Enantioselective Synthesis of Spirobarbiturate-Cyclohexenes through Phosphine-Catalyzed Asymmetric [4 + 2] Annulation of Barbiturate-Derived Alkenes with Allenoates.” Organic Letters, vol. 18, no. 6, Mar. 2016, pp. 1302-1305. https://doi.org/10.1021/acs.orglett.6b00239.
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