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350797-54-5 synthesis

5synthesis methods
1-[3-(Benzoyloxy)propyl]-2,3-dihydro-1H-indole-5-carboxaldehyde

350797-52-3
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350797-54-5

350797-54-5
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-

Yield:-

Steps:

Multi-step reaction with 2 steps
1: ammonium acetate; acetic acid / 4 h / 80 °C
2: sodium tetrahydroborate / dichloromethane; methanol / 1 h / 0 - 25 °C

References:

Zhao, Fei;Li, Jing;Chen, Ying;Tian, Yanxin;Wu, Chenglin;Xie, Yanan;Zhou, Yu;Wang, Jiang;Xie, Xin;Liu, Hong [Journal of Medicinal Chemistry,2016,vol. 59,# 8,p. 3826 - 3839]

350797-53-4 Synthesis
1H-Indole-1-propanol, 2,3-dihydro-5-(2-nitro-1-propen-1-yl)-, 1-benzoate

350797-53-4
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350797-54-5

350797-54-5
5 suppliers
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