Polymer-supported (-)-8-phenylmenthyl Auxiliary as an Effective Solid-phase Chiral Inductor in the Addition of Nucleophiles to N-acyliminium Ions

被引:3
作者
Forero-Doria, Oscar [1 ]
Santos, Leonardo S. [1 ]
Nachtigall, Fabiane M. [2 ]
Shankaraiah, Nagula [3 ]
机构
[1] Talca Univ, Chem Inst Nat Resources, Lab Asymmetr Synth, Talca, Chile
[2] Univ Talca, Inst Innovac Basada Ciencia, Talca, Chile
[3] Natl Inst Pharmaceut Educ & Res NIPER, Dept Med Chem, Hyderabad, Andhra Pradesh, India
关键词
(-)-8-Phenylmenthyl chiral auxiliary; solid-phase synthesis; asymmetric nucleophilic addition; alkaloids; MALDI-MS; on-line monitoring; ENANTIOSELECTIVE TOTAL-SYNTHESIS; CATION POOL; CARBON; ALKYLATION; GENERATION; REDUCTION; STRATEGY; IMINES;
D O I
10.2174/1386207320666170602085724
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aim and Objective: According to our interest in developing new methods for the construction of intricate molecules, a reliable polymer-supported (-)-8-phenylmenthyl chiral auxiliary for the addition of different nucleophiles to chiral-supported N-acyliminium precursors were developed. Materials and Methods: Merrifield resin was employed to anchor (-)-8-phenylmenthol, which was prepared by nitration of (-)-8-phenylmenthyl chloroacetate followed by reduction of nitro group and subsequent Merrifield resin coupling. Treatment of a suspension of polymer-supported chloroformate and piperidinone in the presence of Et3N resulted in attachment of the substrate onto the solid-support. Treatment of the resulting resin with LiEt3BH/MeOH afforded methoxypiperidine in 87% yield. Then, the addition of allyltrimethylsilane, TMSCN, 2-(trimethylsiloxy) propene and triisopropylsilyloxyfuran and others to the N-acyliminium ion derived from chiral 2-methoxypiperidine carbamate was studied. Results: The stereochemical outcome of the addition of nucleophiles to the supported N-acyliminium ion derived from 2-methoxypiperidine carbamate was proposed through the Si- face, affording after resin cleavage 2-substituted piperidines in 70%-84% yields and selectivities ranging from 4:1-11.1. Moreover, the key intermediates of chiral piperidines have been employed for the synthesis of simple chiral alkaloids such as (R)-pipecolic acid, (R)-pelletierine, (S)-coniine and (R,R)-myrtine. Conclusion: The proposed supported-chiral auxiliary for asymmetric approach may be expected to result not only in efficient solid-phase syntheses of a wide range of alkaloids but also in the development of useful new solid-phase methodologies, particularly for the asymmetric additions to iminium precursors. This work describes the first example of solid-phase synthesis by using supported (-)-8-phenylmenthyl as an effective chiral inductor and would be useful for the synthesis of chiral building block libraries.
引用
收藏
页码:696 / 702
页数:7
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