Organocatalytic enantioselective (3+2) cycloaddition using stable azomethine ylides.
نویسندگان
چکیده
We have developed a highly efficient procedure for carrying out the catalytic enantioselective (3+2) cycloaddition between enals and stable azomethine ylides such as isoquinolinium and phthalizinium methylides. Under the optimized reaction conditions highly substituted chiral pyrroloisoquinolines and pyrrolophthalazines have been obtained in high yields and excellent diastereo- and enantioselectivities.
منابع مشابه
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ورودعنوان ژورنال:
- Chemical communications
دوره 47 45 شماره
صفحات -
تاریخ انتشار 2011