Late-Stage Chloride Displacements Enable Access to Peptoids with cis-Inducing Alkylammonium Side Chains.
Late-Stage Chloride Displacements Enable Access to Peptoids with cis-Inducing Alkylammonium Side Chains.
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后期氯化物置换能够获得具有顺式诱导烷基铵侧链的类肽。
DOI:
10.1021/acs.orglett.3c02393
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发表时间:
2023
期刊:
影响因子:
5.2
通讯作者:
Proulx,Caroline
中科院分区:
文献类型:
--
作者:
Davern,CarolynnM;Proulx,Caroline
The synthesis of peptoids possessing multiplecis-inducing monomers with alkylammonium side chains is reported, where chloropropyl side chains are diversified on a solid support by late-stage SN2 displacements with amines. The conditions were optimized for a wide variety of primary, secondary, and tertiary alkyl amine nucleophiles. We also demonstrated that multiple chloride displacements could be achieved on sequences possessingtrans-inducingN-aryl- andN-imino glycine monomers.
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