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. 2020 Nov 2;21(21):8199. doi: 10.3390/ijms21218199

Table 1.

N-arylamine oxetanes obtained via Buchwald–Hartwig Reaction.

Entry Halide/Triflate Product Yield
(%) a
1 graphic file with name ijms-21-08199-i001.jpg graphic file with name ijms-21-08199-i002.jpg 16a: W = H
16b: W = 2,4-di-F
16c: W = 2-CF3
16d: W = 4-OCH3
86
73
77
86
2 graphic file with name ijms-21-08199-i003.jpg graphic file with name ijms-21-08199-i004.jpg 17a: W = H
17b: W = 2,4-di-F
17c: W = 2-CF3
17d: W = 2-OCH3
92
51
82
82
3 graphic file with name ijms-21-08199-i005.jpg graphic file with name ijms-21-08199-i006.jpg 18a: W = H
18b: W = 2,4-di-F
18c: W = 2-CF3
18d: W = 2-OCH3
71
76
95
80
4 graphic file with name ijms-21-08199-i007.jpg graphic file with name ijms-21-08199-i008.jpg 19a: W = H
19b: W = 2,4-di-F
19c: W = 2-CF3
19d: W = 2-OCH3
83
71
88
81
5 b graphic file with name ijms-21-08199-i009.jpg graphic file with name ijms-21-08199-i010.jpg 20a: W = H
20b: W = 2,4-di-F
20c: W = 4-CF3
20d: W = 4-OCH3
20e: W = 4-CN
85
66
71
54
70

a Isolated yields after purification by column chromatography. b Products obtained after deprotection of benzyl ether group.