Bioinspired Ether Cyclizations within a π-Basic Capsule Compared to Autocatalysis on π-Acidic Surfaces and Pnictogen-Bonding Catalysts
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Original data for the publication https://doi.org/10.1002/chem.202101548 <strong>Table of Contents</strong> 1. Synthesis 1.1. Compounds <strong>(<em>R*</em>,<em>R*,S</em>)-25 </strong>and<strong> (<em>S*</em>,<em>S*,S</em>)-25</strong> 1.1.1. NMR 1.1.2. Procedure 1.2. Compounds <strong>(<em>R*</em>,<em>R*</em>)-5 </strong>and <strong>(<em>S*</em>,<em>S*</em>)-5</strong> 1.2.1. Chiral GC Data 1.2.2. Procedure 1.3. Compound <strong>34</strong> 1.3.1. NMR 1.3.2. Procedure 1.4. Compound <strong>35</strong> 1.4.1. NMR 1.4.2. Procedure 1.5. Compound <strong>(<em>R*</em>)-3</strong> 1.5.1. Procedure 1.6. Compound <strong>(<em>S*</em>)-6</strong> 1.6.1. Chiral GC Data 1.6.2. Procedure 2. Kinetic Studies 2.1. Table S1 2.1.1. NMR Spectra for Table S1 2.1.2. Procedures with Anion-pi Catalyst <strong>10</strong> 2.1.3 Procedures with Capsule <strong>15</strong> 2.2. Table S2 2.2.1. NMR Spectra for Table S2 2.2.2. Procedures with Anion-pi Catalyst <strong>10</strong> 2.2.3 Procedures with Capsule <strong>15</strong> 2.3. Table S3 2.3.1. NMR Spectra for Table S3 2.3.2. Procedures with Anion-pi Catalyst <strong>10</strong> 2.3.3 Procedures with Capsule <strong>15</strong> 3. Catalysis 3.1. Co-Catalyst Screening 3.1.1. NMR Spectra for Scheme S3 3.1.2. Procedures with Anion-pi Catalyst <strong>11</strong> 3.2 Catalyst Comparison on the Mono-Epoxide Level 3.2.1. NMR Spectra for Scheme S4 3.2.2. Procedures with Different Catalysts 3.3. Catalyst Comparison on the Di-Epoxide Level 3.3.1. NMR Spectra for Scheme S5 3.3.2. Procedures with Different Catalysts 3.4. Asymmetric Autocatalysis Assay 3.4.1. Chiral GC Data for Schemes S20 and S21 3.4.2. Procedures with Different Substrates
本数据集对应论文https://doi.org/10.1002/chem.202101548的原始数据 <strong>目录</strong> 1. 合成 1.1. 化合物<strong>(*R*,*R*,*S*)-25</strong>与<strong>(*S*,*S*,*S*)-25</strong> 1.1.1. 核磁共振波谱(Nuclear Magnetic Resonance, NMR) 1.1.2. 实验步骤 1.2. 化合物<strong>(*R*,*R*)-5</strong>与<strong>(*S*,*S*)-5</strong> 1.2.1. 手性气相色谱(Chiral GC)数据 1.2.2. 实验步骤 1.3. 化合物<strong>34</strong> 1.3.1. 核磁共振波谱数据 1.3.2. 实验步骤 1.4. 化合物<strong>35</strong> 1.4.1. 核磁共振波谱数据 1.4.2. 实验步骤 1.5. 化合物<strong>(*R*)-3</strong> 1.5.1. 实验步骤 1.6. 化合物<strong>(*S*)-6</strong> 1.6.1. 手性气相色谱数据 1.6.2. 实验步骤 2. 动力学研究 2.1. 补充表S1 2.1.1. 补充表S1对应的核磁共振波谱 2.1.2. 采用阴离子-π催化剂(Anion-pi Catalyst)<strong>10</strong>的实验步骤 2.1.3. 采用胶囊催化剂(Capsule)<strong>15</strong>的实验步骤 2.2. 补充表S2 2.2.1. 补充表S2对应的核磁共振波谱 2.2.2. 采用阴离子-π催化剂<strong>10</strong>的实验步骤 2.2.3. 采用胶囊催化剂<strong>15</strong>的实验步骤 2.3. 补充表S3 2.3.1. 补充表S3对应的核磁共振波谱 2.3.2. 采用阴离子-π催化剂<strong>10</strong>的实验步骤 2.3.3. 采用胶囊催化剂<strong>15</strong>的实验步骤 3. 催化研究 3.1. 助催化剂筛选 3.1.1. 补充方案S3对应的核磁共振波谱 3.1.2. 采用阴离子-π催化剂<strong>11</strong>的实验步骤 3.2. 单环氧化物层面的催化剂对比 3.2.1. 补充方案S4对应的核磁共振波谱 3.2.2. 采用不同催化剂的实验步骤 3.3. 双环氧化物层面的催化剂对比 3.3.1. 补充方案S5对应的核磁共振波谱 3.3.2. 采用不同催化剂的实验步骤 3.4. 不对称自催化测定 3.4.1. 补充方案S20与S21对应的手性气相色谱数据 3.4.2. 采用不同底物的实验步骤



