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Current Organic Synthesis

Editor-in-Chief

ISSN (Print): 1570-1794
ISSN (Online): 1875-6271

Review Article

Tin Powder-Mediated One-Pot Protocols for Allylation Reactions by Allylic Halides

Author(s): Nibras Ahmed Elaas, Waggas Ahmed Elaas, Danfeng Huang, Yulai Hu* and Ke-Hu Wang

Volume 14, Issue 8, 2017

Page: [1156 - 1171] Pages: 16

DOI: 10.2174/1570179414666170201150313

Price: $65

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Abstract

Background: Tin-promoted allylation of carbonyl or imino groups is one of the most convenient and efficient methods for synthesis of homoallylic compounds, which are versatile building blocks in the preparation of many biologically active molecules and natural products.

Objective: This review provides an insight into one-pot allylation reactions for the synthesis of different homoallylic compounds promoted by tin powder.

Conclusion: In the last four decades, tin powder-promoted allylation process has been exploited in synthesis of homoallylic compounds. This multicomponent “one-pot” strategy avoids a lengthy separation process and purification of the intermediate chemical compounds, which saves time and resources while increasing the chemical yield. This tin-promoted process has the following features: operational simplicity, good tolerance to functional groups and improved yields. The protocol could be carried out under wet conditions or even in pure water.

Keywords: Tin powder, One-Pot, allylation reaction, allylic bromide, homoallylic alcohol, homoallylic amines.

Graphical Abstract

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