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. Author manuscript; available in PMC: 2013 Jun 1.
Published in final edited form as: J Org Chem. 2012 Jul 31;78(5):1753–1759. doi: 10.1021/jo3011792

Table 1.

(4+3) Cycloadditions of Oxyallyls with Disubstituted Furans.a

graphic file with name nihms-463527-f0004.jpg
furan syn-I anti-I syn-II anti-II yield (%)
graphic file with name nihms-463527-t0005.jpg graphic file with name nihms-463527-t0006.jpg 67b
graphic file with name nihms-463527-t0007.jpg graphic file with name nihms-463527-t0008.jpg 60b
graphic file with name nihms-463527-t0009.jpg graphic file with name nihms-463527-t0010.jpg graphic file with name nihms-463527-t0011.jpg graphic file with name nihms-463527-t0012.jpg 61c
graphic file with name nihms-463527-t0013.jpg graphic file with name nihms-463527-t0014.jpg 40b
a

Isolated yields are quoted. Isomer ratios are given in parentheses and were determined by 1H and/or 13C NMR.

b

From reaction with allenamide 1b.

c

From reaction with allenamide 1c.