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. 2009 Dec 16;14(12):5298–5307. doi: 10.3390/molecules14125298

Table 1.

Diastereoselectivity of iodine-promoted carbamate annulations.

graphic file with name molecules-14-05298-i001.jpg
Entry Alkenylamine Carbamate Diastereoselectivity Yielda
1 graphic file with name molecules-14-05298-i002.jpg graphic file with name molecules-14-05298-i005.jpg > 20:1 95%
2b graphic file with name molecules-14-05298-i003.jpg graphic file with name molecules-14-05298-i006.jpg > 20:1 93%
3b graphic file with name molecules-14-05298-i004.jpg graphic file with name molecules-14-05298-i007.jpg > 20:1 99%

a Isolated yield. b See reference [11].