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Table 1 Preparation of resveralogues

From: A facile, stereoselective, one-pot synthesis of resveratrol derivatives

 

R’

R

Yield (%)

1

2-CN

3,5-dimethoxy

71

2

3-Cl

4-N(Me)2

79

3

2-NO2

3,5-dimethoxy

80

4

2-F

3,5-dimethoxy

74

5

2-NO2

4-OMe

79

6

3-Cl

3,5-dimethoxy

68

7

3-CF3

4-N(Me)2

74

8

3,5-dimethyl

3,5-dimethoxy

81

9

2,4-difluoro

3,5-dimethoxy

74

10

4-Me

3,5-dimethoxy

84

11

4-CN

3,5-dimethoxy

80

12

4-OMe

3,5-dimethoxy

60

13

4-COOMe

3,5-dimethoxy

59

14

4-NO2

3,5-dimethoxy

90

15

2,6-difluoro

3,5-dimethoxy

78

16

2,6-dichloro

3,5-dimethoxy

79

  1. R’ being the substituent(s) of the benzyl bromide starting material and R, the aldehyde