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. Author manuscript; available in PMC: 2014 Feb 20.
Published in final edited form as: Bioconjug Chem. 2013 Jan 16;24(2):215–223. doi: 10.1021/bc3005073

Table 3.

Preparation of the merocyanine library

graphic file with name nihms438284t13.jpg
acceptor
graphic file with name nihms438284t14.jpg graphic file with name nihms438284t15.jpg graphic file with name nihms438284t16.jpg graphic file with name nihms438284t17.jpg graphic file with name nihms438284t18.jpg

graphic file with name nihms438284t19.jpg I-Pht (82)a I-BA (89) I-SO (97) I-TBA (93) I-Pz (87)
donor graphic file with name nihms438284t20.jpg O-Pht (59) O-BA (29) O-SO (29) O-TBA (85) O-Pz (78)
graphic file with name nihms438284t21.jpg S-Pht (72) S-BA (70) S-SO (78) S-TBA (93) S-Pz (70)
graphic file with name nihms438284t22.jpg TD-Pht (82) TD-BA (61) TD-SO (77) TD-TBA (70) TD-Pz (53)
graphic file with name nihms438284t23.jpg Q-Pht (56) Q-BA (45) Q-SO (20) Q-TBA (69) Q-Pz (39)
a

compound name (% yield)