Ring Expansion Strategies for the Synthesis of Medium Sized Ring and Macrocyclic Sulfonamides
Zhongzhen Yang, Illya Zalessky, Ryan G. Epton, Adrian Charles Whitwood, Jason M. Lynam, William P. Unsworth
Abstract
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Zhongzhen Yang, Illya Zalessky, Ryan G. Epton, Adrian Charles Whitwood, Jason M. Lynam, William P. Unsworth
Abstract
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Abstract Two new ring expansion strategies are reported for the synthesis of medium sized ring and macrocyclic sulfonamides. Both methods can be performed without using classical protecting groups, with the key ring expansion step initiated by nitro reduction and amine conjugate addition respectively. Each method can be used to make diversely functionalised cyclic sulfonamides in good to excellent yields, in a range of ring sizes. The ring size dependency of the synthetic reactions is in good agreement with the outcomes modelled by Density Functional Theory calculations.
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Abstract Two new ring expansion strategies are reported for the synthesis of medium sized ring and macrocyclic sulfonamides. Both methods can be performed without using classical protecting groups, with the key ring expansion step initiated by nitro reduction and amine conjugate addition respectively. Each method can be used to make diversely functionalised cyclic sulfonamides in good to excellent yields, in a range of ring sizes. The ring size dependency of the synthetic reactions is in good agreement with the outcomes modelled by Density Functional Theory calculations.
Key concepts: Ring (chemistry), Conjugate, Ring size, Chemistry, Amine gas treating, Combinatorial chemistry, Organic chemistry, Mathematics