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. Author manuscript; available in PMC: 2013 Jul 16.
Published in final edited form as: Chem Biol Drug Des. 2012 Jan 30;79(4):470–477. doi: 10.1111/j.1747-0285.2011.01288.x

Table 1.

Varations of isocyanides and praziquantel derivatives 8(a-e)graphic file with name nihms-343095-t0003.jpg

Entry R1NC
2(a-h)
Product 8
(a-e)
Yield (%)
1 graphic file with name nihms-343095-t0004.jpg graphic file with name nihms-343095-t0005.jpg 8a 46c
2 graphic file with name nihms-343095-t0006.jpg graphic file with name nihms-343095-t0007.jpg 8b 48c
3 graphic file with name nihms-343095-t0008.jpg graphic file with name nihms-343095-t0009.jpg 8c 34c
4 graphic file with name nihms-343095-t0010.jpg graphic file with name nihms-343095-t0011.jpg 8d a 16c
5 graphic file with name nihms-343095-t0012.jpg graphic file with name nihms-343095-t0013.jpg 8e b 45c
6 graphic file with name nihms-343095-t0014.jpg - - 76d
7 graphic file with name nihms-343095-t0015.jpg - - 73d
8 graphic file with name nihms-343095-t0016.jpg - - 58d
a

Only trans-8d was identified.

b

Two diastereomers were isolated in a ratio of 2.4:1 (trans/cis).

c

Overall isolated yield for two steps.

d

Isolated yield for the Ugi reaction.