, 3H) ppm. 13 C{ 1 H} NMR (100 MHz, CDCl3): ? = 167, vol.6

, Mp: 88-90 o C. 1 H NMR (400 MHz, CDCl3): ? = 8.01 (dd, -Oxoisoindolin-2-yl)phenyl 2-fluorobenzoate (2r): 65.6 mg (63% yield), white solid

D. and J. , Hz, 1H), 4.80 (s, 2H) ppm. 13 C{ 1 H} NMR (100 MHz, CDCl3): ? = 167.6, 166.2 (d, JC-F = 259.9 Hz), vol.162

, F{ 1 H} NMR (376 MHz, CDCl3): ? = -108.8 ppm. HRMS (ESI) calcd. for

, -Oxoisoindolin-2-yl)phenyl 2-chlorobenzoate (2s): 38.9 mg (36% yield), yellow solid, Mp: 110-112 o C. 1H NMR (400 MHz, CDCl3): ? = 7.95 (d, J = 7.6 Hz, 1H), 7.87 (d, J = 7.6 Hz, 1H), 7.55 (dd, J = 7.6, 7.2 Hz, 1H), 7.48-7.37 (m, 8H), 7.29-7.23 (m, 1H), 4.80 (s, 2H) ppm. 13 C{ 1 H} NMR (100 MHz, CDCl3): ? = 167

, -Oxoisoindolin-2-yl)phenyl 2-naphthoate (2t): 70.3 mg (62% yield), yellow solid, Mp: < 50 o C. 1 H NMR

, ? = 8.67 (s, 1H), 8.07 (d, J = 8.4 Hz, 1H), 7.88-7.82 (m, 4H), 7.60-7.37 (m, 9H), 4.80 (s, 2H) ppm. 13 C{ 1 H} NMR (100 MHz, CDCl3): ? = 167

, -Oxoisoindolin-2-yl)phenyl thiophene-2-carboxylate

, mg (77% yield), yellow solid, Mp: < 50 o C. 1H NMR, p.400

C. Mhz, ? = 7.86 (d, J = 7.6 Hz, 1H), 7.57-7.36 (m, 8H), vol.7

, C{ 1 H} NMR (100 MHz, CDCl3): ? = 167.6, 156.3, 147.5, 145.9

, Mp: < 50 o C. 1 H NMR (400 MHz, CDCl3): ? = 7.86 (d, J = 7.6 Hz, 1H), 7.57-7.36 (m, 8H), vol.7

. Hz,

, C{ 1 H} NMR (100 MHz, CDCl3): ? = 167.6, 156.3, 147.5, 145.9

, -Hydroxyphenyl)isoindolin-1-one (3): 40.9 mg (63% yield), colourless solid, 1 H NMR (400 MHz, CDCl3): ? = 8.82 (br, 1H), 7.93 (d, J = 7.6 Hz, 1H), 7.64 (dd, J = 7.6, 7.2 Hz, 1H), 7.56-7.52 (m, 2H), 7.25-7

C. Mhz, The spectral data match those previously reported, vol.132, p.11

, mg (23% yield), white solid, Mp: 205-207 o C. 1 H NMR (400 MHz, CDCl3): ? = 9

, Hz, 1H), 7.68-7.64 (m, 2H), 7.58-7.54 (m, 2H), 7.27 (d, J = 8.0 Hz, 1H), 5.00 (s, 2H), 4.37 (q, J = 7.2 Hz, 2H), 1.40 (t, J = 7.2 Hz, 3H) ppm. 13 C{ 1 H} NMR (100 MHz, CDCl3): ? = 169

, 68.8 mg (49% yield), brown oil. 1H NMR (400 MHz, CDCl3): ? = 8.18 (d, J = 7

, Hz, 2H), 7.62 (dd, J = 7.6, 7.2 Hz, 1H), 7.49 (dd, J = 7.6, 7.6 Hz, 2H), 7.38-7.27 (m, 4H), 3.71 (t, J = 7.2 Hz, 2H), 2.36 (t, J = 8.0 Hz, 2H), 2.05-1.97 (m, 2H) ppm. 13 C{ 1 H} NMR (100 MHz, CDCl3): ?

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