Enantioselective addition of activated terminal alkynes to 1-acylpyridinium salts catalyzed by Cu-bis(oxazoline) complexes
Sun ZK(孙占奎) ; Yu SY(俞寿云) ; Ding ZD(丁左定) ; Ma DW(马大为)
刊名J. Am. Chem. Soc.
2007
卷号129期号:30页码:9300-9301
ISSN号0002-7863
其他题名酮噁唑啉配体催化的末端炔烃对1-吡啶酰氯鎓盐的对映选择性的加成
通讯作者马大为
英文摘要CuI/bis(oxazoline)-catalyzed addition of propiolates and terminal ynones to 1-acylpyridinium salt (generated in situ from reaction of pyridine and methyl chloroformate) affords highly functionalized dihydropyridines with excellent enantioselectivity. It is found that the carbonyl group adjacent to the alkyne moiety is essential for the enantioselectivity of the addition. Short synthesis of indolizidines 167B and 223AB is achieved by employing two addition products.
学科主题有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ja0734849
语种英语
WOS记录号WOS:000248281100027
公开日期2013-02-19
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/15543]  
专题上海有机化学研究所_生命有机化学国家重点实验室
推荐引用方式
GB/T 7714
Sun ZK,Yu SY,Ding ZD,et al. Enantioselective addition of activated terminal alkynes to 1-acylpyridinium salts catalyzed by Cu-bis(oxazoline) complexes[J]. J. Am. Chem. Soc.,2007,129(30):9300-9301.
APA 孙占奎,俞寿云,丁左定,&马大为.(2007).Enantioselective addition of activated terminal alkynes to 1-acylpyridinium salts catalyzed by Cu-bis(oxazoline) complexes.J. Am. Chem. Soc.,129(30),9300-9301.
MLA 孙占奎,et al."Enantioselective addition of activated terminal alkynes to 1-acylpyridinium salts catalyzed by Cu-bis(oxazoline) complexes".J. Am. Chem. Soc. 129.30(2007):9300-9301.
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