(5S*,6R*,7R*)-6-Formyl-5-phenyl-7- propylperhydropyrazolo[1,2-a]pyrazol-1-one

Jinlan Yu; Qingshan Zhang; Yanhong Liu; Yunzheng Li; Qinpei Wu

doi:10.1107/S1600536810016764

(5S,6R,7R*)-6-Formyl-5-phenyl-7- propylperhydropyrazolo[1,2-a]pyrazol-1-one

Jinlan Yu
, Qingshan Zhang
, Yanhong Liu
, Yunzheng Li
, Qinpei Wu^*

^*此作品的通讯作者

化学与化工学院

Beijing Institute of Technology
CAS - Technical Institute of Physics and Chemistry

科研成果: 期刊稿件 › 文章 › 同行评审

1 引用（Scopus）

摘要

The title compound, C₁₆H₂₀N₂O₂, was obtained by catalytic asymmetric cyclo-addition of trans-3-propyl-acrolein with 1-benzylidenepyrazolid-3-one betaine. There are two symmetry-independent molecules in the asymmetric unit. In both molecules, the two five-membered heterocyclic rings adopt envelope conformations.

源语言	英语
页（从-至）	o1572
期刊	Acta Crystallographica Section E: Structure Reports Online
卷	66
期	7
DOI	https://doi.org/10.1107/S1600536810016764
出版状态	已出版 - 2010

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10.1107/S1600536810016764

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@article{d9e8bf07367148b69bd2d539fc705304,

title = "(5S*,6R*,7R*)-6-Formyl-5-phenyl-7- propylperhydropyrazolo[1,2-a]pyrazol-1-one",

abstract = "The title compound, C16H20N2O2, was obtained by catalytic asymmetric cyclo-addition of trans-3-propyl-acrolein with 1-benzylidenepyrazolid-3-one betaine. There are two symmetry-independent molecules in the asymmetric unit. In both molecules, the two five-membered heterocyclic rings adopt envelope conformations.",

author = "Jinlan Yu and Qingshan Zhang and Yanhong Liu and Yunzheng Li and Qinpei Wu",

year = "2010",

doi = "10.1107/S1600536810016764",

language = "English",

volume = "66",

pages = "o1572",

journal = "Acta Crystallographica Section E: Structure Reports Online",

issn = "1600-5368",

publisher = "International Union of Crystallography",

number = "7",

}

TY - JOUR

T1 - (5S*,6R*,7R*)-6-Formyl-5-phenyl-7- propylperhydropyrazolo[1,2-a]pyrazol-1-one

AU - Yu, Jinlan

AU - Zhang, Qingshan

AU - Liu, Yanhong

AU - Li, Yunzheng

AU - Wu, Qinpei

PY - 2010

Y1 - 2010

N2 - The title compound, C16H20N2O2, was obtained by catalytic asymmetric cyclo-addition of trans-3-propyl-acrolein with 1-benzylidenepyrazolid-3-one betaine. There are two symmetry-independent molecules in the asymmetric unit. In both molecules, the two five-membered heterocyclic rings adopt envelope conformations.

AB - The title compound, C16H20N2O2, was obtained by catalytic asymmetric cyclo-addition of trans-3-propyl-acrolein with 1-benzylidenepyrazolid-3-one betaine. There are two symmetry-independent molecules in the asymmetric unit. In both molecules, the two five-membered heterocyclic rings adopt envelope conformations.

UR - https://www.scopus.com/pages/publications/77954409990

U2 - 10.1107/S1600536810016764

DO - 10.1107/S1600536810016764

M3 - Article

AN - SCOPUS:77954409990

SN - 1600-5368

VL - 66

SP - o1572

JO - Acta Crystallographica Section E: Structure Reports Online

JF - Acta Crystallographica Section E: Structure Reports Online

IS - 7

ER -

(5S*,6R*,7R*)-6-Formyl-5-phenyl-7- propylperhydropyrazolo[1,2-a]pyrazol-1-one

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(5S,6R,7R*)-6-Formyl-5-phenyl-7- propylperhydropyrazolo[1,2-a]pyrazol-1-one