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. Author manuscript; available in PMC: 2014 Oct 1.
Published in final edited form as: Synthesis (Stuttg). 2013 Oct 1;45(19):2699–2705. doi: 10.1055/s-0033-1338419

Table 2.

Scope studies for hydroxamic acid synthesis.

entrya product yield (%)b
1 graphic file with name nihms529044t1.jpg R7 = H 83
2 R7 = OMe 77
3 R7 = Me 85
4 R7 = CF3 81
5 R7 = CN 72
6 R7 = Br 76
7 graphic file with name nihms529044t2.jpg R6 = F 79
8 R6 = OMe 0c
9 graphic file with name nihms529044t3.jpg X = O 78
10d X = NTs 53
11d graphic file with name nihms529044t4.jpg 64
12d graphic file with name nihms529044t5.jpg 58
a

Reactions conducted using 2.5 mol% Ru(bpy)3Cl2, 2.1 equiv 5, and 0.1 equiv CSA unless otherwise noted.

b

Values represent the averaged isolated yields from two reproducible experiments.

c

Quinolinone 10 was isolated in 54% yield (Scheme 2).

d

Reaction conducted using 3 equiv of 5 and 1 equiv of CSA.