FeCl3-catalyzed cyclization of alpha-sulfonamido-allenes with aldehydes-the substituent effect
Cheng JJ(成佳佳) ; Tang XJ(汤鑫军) ; Yu YH(余亦华) ; Ma SM(麻生明)
刊名Chem. Commun.
2012
卷号48期号:99页码:12074-12076
ISSN号1359-7345
其他题名FeCl3-催化的α-亚磺酰氨基-联烯和醛的环化反应及其取代基效应
通讯作者麻生明
英文摘要FeCl3-catalyzed aza-Prins-cyclization reaction of alpha-sulfonamido-allenes with aldehydes afforded 1,2,3,6-tetrahydropyridine or 2,5-dihydro-1H-pyrrole derivatives efficiently and highly selectively. The different regioselectivity is probably caused by the stabilizing effect of the phenyl group on the positively charged allylic intermediate.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c2cc36941a
语种英语
WOS记录号WOS:000311287500010
公开日期2013-08-22
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/28183]  
专题上海有机化学研究所_金属有机化学国家重点实验室
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GB/T 7714
Cheng JJ,Tang XJ,Yu YH,et al. FeCl3-catalyzed cyclization of alpha-sulfonamido-allenes with aldehydes-the substituent effect[J]. Chem. Commun.,2012,48(99):12074-12076.
APA 成佳佳,汤鑫军,余亦华,&麻生明.(2012).FeCl3-catalyzed cyclization of alpha-sulfonamido-allenes with aldehydes-the substituent effect.Chem. Commun.,48(99),12074-12076.
MLA 成佳佳,et al."FeCl3-catalyzed cyclization of alpha-sulfonamido-allenes with aldehydes-the substituent effect".Chem. Commun. 48.99(2012):12074-12076.
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