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Diastereoselective Synthesis of Dispiropyrrolidinyloxindoles via DBU-Promoted [3+2]-Cycloaddition of Cyclic Pyridinium Ylides and α,β-Unsaturated Ketones
被引:2
|作者:
Liang, Xiayu
[1
]
Wang, Bingren
[1
]
Sun, Jiayang
[1
]
Li, Yaqi
[2
]
Zeng, Qingle
[1
]
机构:
[1] Chengdu Univ Technol, Coll Mat Chem & Chem Engn, State Key Lab Geohazard Prevent & Geoenvironm Prot, Chengdu 610059, Peoples R China
[2] Hunan Normal Univ, Coll Life Sci, Natl & Local Joint Engn Lab Anim Peptide Drug Dev, Changsha 410012, Peoples R China
关键词:
3+2]-cycloaddition;
alpha;
beta-unsaturated ketones;
dispiropyrrolidinyloxindoles;
DBU;
pyridinium ylides;
FACILE SYNTHESIS;
1,3-DIPOLAR CYCLOADDITION;
AZOMETHINE YLIDES;
ANTICANCER;
ANTIMYCOBACTERIAL;
CONSTRUCTION;
POTENT;
D O I:
10.1002/ajoc.202200681
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A novel [3+2]-cycloaddition reaction of cyclic pyridinium ylides and alpha,beta-unsaturated ketones derived from indanones for the synthesis of dispiropyrrolidinyloxindoles is described herein. Various types of dispiropyrrolidinyloxindoles can be conveniently accessed with moderate to good yields and up to > 99 : 1 dr from easily available pyridinium salts which bear an electron-withdrawing group on the pyridine ring under mild conditions for short reaction time.
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页数:6
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