Crystallography Open Database
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COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1547821 | CIF | C18 H17 N O3 | C 1 2/c 1 | 16.581; 10.7796; 17.25 90; 102.204; 90 | 3013.5 | Samineni, Ramesh; Madapa, Jaipal; Pabbaraja, Srihari; Mehta, Goverdhan Stitching Oxindoles and Ynones in a Domino Process: Access to Spirooxindoles and Application to a Short Synthesis of Spindomycin B. Organic letters, 2017, 19, 6152-6155 |
| 1547822 | CIF | C16 H19 B O4 | P 1 21/c 1 | 6.538; 16.718; 13.471 90; 90.09; 90 | 1472.4 | Murai, Masahito; Mizuta, Chisato; Taniguchi, Ryuji; Takai, Kazuhiko Synthesis of Borylcyclopropanes by Chromium-Promoted Cyclopropanation of Unactivated Alkenes. Organic letters, 2017, 19, 6104-6107 |
| 1547823 | CIF | C16 H26.5 O7.25 | I 1 2 1 | 19.911; 5.551; 30.35 90; 95.908; 90 | 3337 | Hurtak, Jessica A.; McDonald, Frank E. Synthesis of the ABC Substructure of Brevenal by Sequential exo-Mode Oxacyclizations of Acyclic Polyene Precursors. Organic letters, 2017, 19, 6036-6039 |
| 1547824 | CIF | C15 H25 I O5 | P 21 21 21 | 10.02693; 11.10793; 14.3797 90; 90; 90 | 1601.59 | Hurtak, Jessica A.; McDonald, Frank E. Synthesis of the ABC Substructure of Brevenal by Sequential exo-Mode Oxacyclizations of Acyclic Polyene Precursors. Organic letters, 2017, 19, 6036-6039 |
| 1547825 | CIF | C19 H18 O4 | P 1 21/n 1 | 10.697; 9.009; 16.863 90; 106.217; 90 | 1560.4 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547826 | CIF | C26 H25 N O5 S | P 1 21/c 1 | 14.411; 12.274; 13.749 90; 112.87; 90 | 2240.8 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547827 | CIF | C24 H27 N O5 S | P -1 | 9.304; 10.764; 11.843 98.386; 96.739; 109.699 | 1086.9 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547828 | CIF | C28 H29 N O6 S | P 1 21/n 1 | 8.72; 21.854; 13.387 90; 104.956; 90 | 2464.7 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547829 | CIF | C22 H22 N2 O8 | P -1 | 9.377; 10.292; 12.467 75.494; 70.702; 64.502 | 1016.7 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547830 | CIF | C16 H18 O4 | P 1 21/n 1 | 11.1174; 8.648; 14.313 90; 92.161; 90 | 1375.1 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547831 | CIF | C17 H20 O3 S | P 1 21/n 1 | 10.5546; 22.9756; 13.1098 90; 98.657; 90 | 3142.9 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547832 | CIF | C17 H21 N O3 | P -1 | 11.018; 11.202; 12.907 76.79; 79.73; 84.52 | 1524 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547833 | CIF | C27 H27 N O5 S | P -1 | 11.246; 11.3077; 11.3931 86.918; 62.751; 68.161 | 1183.6 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547834 | CIF | C24 H29 N O5 S | P 1 21/n 1 | 11.5447; 17.0612; 12.493 90; 113.393; 90 | 2258.4 | Gharpure, Santosh J.; Anuradha, Dandela Synthesis of Benzo[1,4]heterocycles using Palladium Catalyzed Heck Reaction to Vinylogous Carbonates/Carbamates: Unexpected Formation of Indoles via Carbopalladation Intercepted by Nucleopalladation. Organic letters, 2017, 19, 6136-6139 |
| 1547841 | CIF | C23 H24 N2 O5 | P -1 | 10.0991; 10.6816; 11.0208 61.574; 78.04; 87.766 | 1020.4 | Xie, Jialin; Huang, Yuanqiong; Song, Hongjian; Liu, Yuxiu; Wang, Qingmin Copper-Catalyzed Aerobic Oxidative [2 + 3] Cyclization/Aromatization Cascade Reaction: Atom-Economical Access to Tetrasubstituted 4,5-Biscarbonyl Imidazoles. Organic letters, 2017, 19, 6056-6059 |
| 1547842 | CIF | C37 H32 I N3 O3 | C 1 2/c 1 | 18.8797; 13.6265; 24.4476 90; 94.0494; 90 | 6273.8 | Balalaie, Saeed; Mirzaie, Sattar; Nikbakht, Ali; Hamdan, Fatima; Rominger, Frank; Navari, Razieh; Bijanzadeh, Hamid Reza Indium-Catalyzed Intramolecular Hydroamidation of Alkynes: An Exo-Dig Cyclization for the Synthesis of Pyranoquinolines through Post-Transformational Reaction. Organic letters, 2017, 19, 6124-6127 |
| 1547859 | CIF | C23 H18 N2 O2 S | P -1 | 10.817; 11.6749; 16.4638 97.305; 96.365; 108.875 | 1925.64 | Modi, Anju; Sau, Prasenjit; Patel, Bhisma K. Base-Promoted Synthesis of Quinoline-4(1H)-thiones from o-Alkynylanilines and Aroyl Isothiocyanates. Organic letters, 2017, 19, 6128-6131 |
| 1547860 | CIF | C30.16 H25.33 Cl0.33 N O2 | P 65 | 26.4511; 26.4511; 11.7055 90; 90; 120 | 7092.64 | Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles. Organic letters, 2017, 19, 6112-6115 |
| 1547861 | CIF | C32 H28 Br2 N2 O4.5 | C 1 2 1 | 23.9252; 10.3277; 12.9767 90; 98.8598; 90 | 3168.18 | Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles. Organic letters, 2017, 19, 6112-6115 |
| 1547862 | CIF | C31 H25 Br2 Cl3 N2 O4 | P -1 | 9.6966; 10.8744; 15.2236 84.4918; 86.8253; 73.5134 | 1531.48 | Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles. Organic letters, 2017, 19, 6112-6115 |
| 1547863 | CIF | C31.5 H27 F2 N2 O4.5 | C 1 2 1 | 24.0915; 9.3008; 12.4495 90; 99.6191; 90 | 2750.34 | Chaudhari, Prakash D.; Hong, Bor-Cherng; Lee, Gene-Hsiang Organocatalytic Enantioselective Michael-Michael-Michael-Aldol Condensation Reactions: Control of Six Stereocenters in a Quadruple-Cascade Asymmetric Synthesis of Polysubstituted Spirocyclic Oxindoles. Organic letters, 2017, 19, 6112-6115 |
| 1547874 | CIF | C19 H18 N2 O2 S | C 1 2/c 1 | 14.3; 8.3251; 29.9248 90; 99.0075; 90 | 3518.6 | Ramesh, Balu; Jeganmohan, Masilamani Ruthenium-Catalyzed Remote C-H Sulfonylation of N-Aryl-2-aminopyridines with Aromatic Sulfonyl Chlorides. Organic letters, 2017, 19, 6000-6003 |
| 1547875 | CIF | C20 H20 N2 O2 S | C 1 2/c 1 | 14.8321; 8.4143; 29.8348 90; 97.4759; 90 | 3691.8 | Ramesh, Balu; Jeganmohan, Masilamani Ruthenium-Catalyzed Remote C-H Sulfonylation of N-Aryl-2-aminopyridines with Aromatic Sulfonyl Chlorides. Organic letters, 2017, 19, 6000-6003 |
| 1547876 | CIF | C15 H14 N4 O4 | P 1 21/n 1 | 8.006; 12.99; 14.7 90; 100.16; 90 | 1505 | Mondal, Ramij R.; Khamarui, Saikat; Maiti, Dilip K. Photocatalytic Generation of Nitrenes for Rapid Diaziridination. Organic letters, 2017, 19, 5964-5967 |
| 1547905 | CIF | C29 H33 Br O4 | P -1 | 9.8378; 10.0606; 14.0335 70.001; 80.759; 83.195 | 1285.2 | Yang, Jun; Xu, Wenbo; Cui, Qi; Fan, Xing; Wang, Lu-Ning; Yu, Zhi-Xiang Asymmetric Total Synthesis of (-)-Clovan-2,9-dione Using Rh(I)-Catalyzed [3 + 2 + 1] Cycloaddition of 1-Yne-vinylcyclopropane and CO. Organic letters, 2017, 19, 6040-6043 |
| 1547906 | CIF | C23 H24 O2 | P 1 21 1 | 11.9476; 5.9856; 12.3311 90; 93.344; 90 | 880.34 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547907 | CIF | C22 H16 Cl F3 | P b c a | 10.6429; 17.14; 19.551 90; 90; 90 | 3566.5 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547908 | CIF | C22 H20 Cl F O | P 21 21 21 | 5.973; 15.888; 18.3194 90; 90; 90 | 1738.5 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547909 | CIF | C21 H19 N | P 1 21/n 1 | 8.6347; 10.9298; 16.4312 90; 93.191; 90 | 1548.3 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547910 | CIF | C23 H21 Cl | P 1 21/c 1 | 9.7435; 20.96; 9.8864 90; 113.368; 90 | 1853.4 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547911 | CIF | C22 H19 I | P 1 21 1 | 5.7244; 14.8287; 21.3598 90; 97.293; 90 | 1798.47 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547912 | CIF | C23 H23 Cl O | P -1 | 6.4515; 17.1888; 18.0877 68.737; 87.418; 89.422 | 1867.33 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547913 | CIF | C22 H25 N O2 | P -1 | 6.1271; 16.148; 18.8563 90.872; 97.1; 98.775 | 1828.57 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547914 | CIF | C22 H21 Cl O | P 1 21/c 1 | 11.7165; 6.0572; 24.9509 90; 94.48; 90 | 1765.33 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547915 | CIF | C23 H24 O | P 1 21 1 | 5.9827; 25.0699; 11.6168 90; 90.887; 90 | 1742.14 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547916 | CIF | C23 H23 Cl O | P 1 21/c 1 | 18.5748; 6.4645; 15.9299 90; 107.348; 90 | 1825.8 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547917 | CIF | C22 H21 I O | P 1 21/c 1 | 12.1357; 6.0494; 25.0871 90; 96.515; 90 | 1829.84 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547918 | CIF | C22 H19 F | P -1 | 8.9407; 9.6685; 10.3518 113.062; 90.552; 92.535 | 822.17 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547919 | CIF | C23 H24 O | P 1 21/c 1 | 17.524; 5.9716; 16.6106 90; 94.777; 90 | 1732.2 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547920 | CIF | C20 H17 Cl S | P -1 | 8.5228; 12.1509; 17.005 72.107; 89.784; 82.281 | 1659.36 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547921 | CIF | C23 H24 O2 | P 1 21/c 1 | 18.524; 5.7934; 16.9793 90; 105.284; 90 | 1757.7 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547922 | CIF | C22 H19 F | P 1 21/n 1 | 10.1038; 8.9144; 18.5125 90; 95.222; 90 | 1660.5 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547923 | CIF | C23 H22 O | P -1 | 9.5851; 9.9859; 10.2722 78.476; 66.039; 75.513 | 864.54 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547924 | CIF | C21 H19 N | P n a 21 | 13.5127; 9.4159; 25.6168 90; 90; 90 | 3259.3 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547925 | CIF | C21 H21 N O | P 1 | 6.1157; 7.6877; 35.725 88.193; 85.251; 82.371 | 1658.7 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547926 | CIF | C27 H30 O3 | P 1 21/n 1 | 17.0051; 7.463; 18.2727 90; 97.403; 90 | 2299.6 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547927 | CIF | C23 H21 Cl | P -1 | 9.5964; 9.794; 10.906 99.828; 94.064; 118.202 | 876.4 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547928 | CIF | C23 H22 | P 1 21/c 1 | 5.7206; 16.0457; 18.9021 90; 91.033; 90 | 1734.76 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547929 | CIF | C37 H38 N O4 P | P 1 21/c 1 | 10.7335; 14.9683; 20.7298 90; 103.232; 90 | 3242.1 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547930 | CIF | C23 H21 Cl O | P -1 | 5.4926; 9.9685; 18.0281 80.689; 89.091; 74.881 | 940.01 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547931 | CIF | C27 H28 O2 | P 1 21/n 1 | 14.358; 9.3991; 16.714 90; 104.03; 90 | 2188.3 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547932 | CIF | C22 H21 F O | P 1 21 1 | 11.7538; 5.9738; 12.1137 90; 93.451; 90 | 849.02 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547933 | CIF | C23 H22 O | P -1 | 8.7067; 9.2287; 12.614 77.052; 72.793; 64.314 | 867.09 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547934 | CIF | C20 H19 Cl O S | P 21 21 21 | 5.737; 15.6229; 18.8695 90; 90; 90 | 1691.25 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547935 | CIF | C23 H21 Cl O | P 1 21/c 1 | 5.8455; 16.6918; 37.3464 90; 90.567; 90 | 3643.8 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547936 | CIF | C23 H24 O2 | P -1 | 6.5207; 16.0428; 17.9567 83.358; 86.821; 80.353 | 1838.2 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547937 | CIF | C22 H21 F O | P 21 21 21 | 5.8984; 16.5715; 17.3993 90; 90; 90 | 1700.7 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547938 | CIF | C23 H23 Cl O2 | P -1 | 8.2234; 8.767; 13.8661 91.431; 95.956; 110.953 | 926.45 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547939 | CIF | C20 H20 O S | P 21 21 21 | 5.9092; 13.9608; 39.1514 90; 90; 90 | 3229.9 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547940 | CIF | C22 H19 Cl | P 21 21 2 | 16.1056; 18.6607; 5.7399 90; 90; 90 | 1725.08 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1547941 | CIF | C22 H18 Cl F | C 1 2/c 1 | 20.898; 10.2307; 17.2114 90; 109.785; 90 | 3462.6 | Lim, Ngiap-Kie; Weiss, Patrick; Li, Beryl X.; McCulley, Christina H.; Hare, Stephanie R.; Bensema, Bronwyn L.; Palazzo, Teresa A.; Tantillo, Dean J.; Zhang, Haiming; Gosselin, Francis Synthesis of Highly Stereodefined Tetrasubstituted Acyclic All-Carbon Olefins via a Syn-Elimination Approach. Organic letters, 2017, 19, 6212-6215 |
| 1548052 | CIF | C7 H4 Cl2 O2 | P -1 | 6.6783; 7.8355; 8.1648 65.48; 86.218; 72.786 | 370.51 | Chen, Xiao-Yang; Ozturk, Seyma; Sorensen, Erik J. Pd-Catalyzed Ortho C-H Hydroxylation of Benzaldehydes Using a Transient Directing Group. Organic letters, 2017, 19, 6280-6283 |
| 1548125 | CIF | C23 H20 N2 O | P -1 | 7.7845; 10.4296; 11.802 85.724; 74.803; 69.047 | 863.35 | Zhu, Zhengbo; Lv, Xin; Anesini, Jason E.; Seidel, Daniel Synthesis of Polycyclic Imidazolidinones via Amine Redox-Annulation. Organic letters, 2017, 19, 6424-6427 |
| 1548126 | CIF | C29 H24 N2 O | P 1 21/c 1 | 10.6445; 18.8991; 11.1931 90; 109.71; 90 | 2119.81 | Zhu, Zhengbo; Lv, Xin; Anesini, Jason E.; Seidel, Daniel Synthesis of Polycyclic Imidazolidinones via Amine Redox-Annulation. Organic letters, 2017, 19, 6424-6427 |
| 1548127 | CIF | C18 H17 N O4 S | C 1 c 1 | 13.726; 15.964; 7.7194 90; 111.03; 90 | 1578.8 | Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles. Organic letters, 2017, 19, 6268-6271 |
| 1548128 | CIF | C18 H17 N O5 S | P 1 21/c 1 | 6.3553; 14.813; 17.085 90; 95.7; 90 | 1600.4 | Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles. Organic letters, 2017, 19, 6268-6271 |
| 1548129 | CIF | C18 H17 N O5 S | P -1 | 6.1967; 11.195; 12.7835 110.691; 92.738; 93.838 | 825.33 | Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles. Organic letters, 2017, 19, 6268-6271 |
| 1548130 | CIF | C12 H13 N O4 S | P 21 21 21 | 5.7561; 10.135; 20.636 90; 90; 90 | 1203.9 | Wu, Yang; Yuan, Chunhao; Wang, Chang; Mao, Biming; Jia, Hao; Gao, Xing; Liao, Jianning; Jiang, Feng; Zhou, Leijie; Wang, Qijun; Guo, Hongchao Palladium-Catalyzed [5 + 2] Cycloaddition of Vinyloxiranes with Sulfamate-Derived Cyclic Imines To Construct 1,3-Oxazepine Heterocycles. Organic letters, 2017, 19, 6268-6271 |
| 1548606 | CIF | C18 H18 O5 S | P -1 | 9.1078; 9.1877; 11.146 81.945; 68.341; 81.982 | 854.38 | Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives. Organic letters, 2017, 19, 6084-6087 |
| 1548607 | CIF | C24 H26 O7 S | P 1 21/n 1 | 7.584; 23.96; 13.042 90; 95.24; 90 | 2360 | Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives. Organic letters, 2017, 19, 6084-6087 |
| 1548608 | CIF | C24 H25 F O7 S | P -1 | 7.7157; 11.4525; 13.9009 97.178; 95.839; 100.355 | 1189.1 | Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives. Organic letters, 2017, 19, 6084-6087 |
| 1548609 | CIF | C24 H21 Cl O5 S | P -1 | 8.68; 10.624; 12.798 79.965; 74.188; 89.59 | 1117.1 | Jia, Jiru; Yu, Aimin; Ma, Shanshan; Zhang, Youquan; Li, Ke; Meng, Xiangtai Solvent-Controlled Switchable Domino Reactions of MBH Carbonate: Synthesis of Benzothiophene Fused α-Pyran, 2,3-Dihydrooxepine, and Oxatricyclodecene Derivatives. Organic letters, 2017, 19, 6084-6087 |
| 1548610 | CIF | C17 H14 O S2 | P 1 21/c 1 | 9.5414; 17.3999; 9.7984 90; 116.714; 90 | 1453.1 | Wang, Quannan; Yang, Xiaoge; Wu, Ping; Yu, Zhengkun Photoredox-Catalyzed C-H Arylation of Internal Alkenes to Tetrasubstituted Alkenes: Synthesis of Tamoxifen. Organic letters, 2017, 19, 6248-6251 |
| 1548611 | CIF | C17 H13 N3 O3 S2 | P 1 21/n 1 | 4.0165; 23.916; 17.104 90; 94.419; 90 | 1638.1 | Wang, Quannan; Yang, Xiaoge; Wu, Ping; Yu, Zhengkun Photoredox-Catalyzed C-H Arylation of Internal Alkenes to Tetrasubstituted Alkenes: Synthesis of Tamoxifen. Organic letters, 2017, 19, 6248-6251 |
| 1548612 | CIF | C19 H17 Br N2 O2 | P 21 21 21 | 6.2066; 16.3879; 16.6057 90; 90; 90 | 1689 | Yuan, Shiru; Luo, Yuchen; Peng, Jingyi; Miao, Maozhong; Xu, Jianfeng; Ren, Hongjun Oxidative Asymmetric [2 + 3] Annulation of Aldehydes with Azomethine Imines Enabled by N-Heterocyclic Carbene Catalysis. Organic letters, 2017, 19, 6100-6103 |
| 1554753 | CIF | C31 H26 Cl N O4 | P 21 21 21 | 7.9152; 11.4088; 28.388 90; 90; 90 | 2563.5 | He, Zhao-Lin; Sheong, Fu Kit; Li, Qing-Hua; Lin, Zhenyang; Wang, Chun-Jiang Exoselective 1,3-dipolar [3 + 6] cycloaddition of azomethine ylides with 2-acylcycloheptatrienes: stereoselectivity and mechanistic insight. Organic letters, 2015, 17, 1365-1368 |
| 1554755 | CIF | C22 H25 O5 P | P -1 | 7.8931; 9.4542; 14.3399 89.1605; 82.9814; 69.4905 | 994.29 | Kim, Cheol-Eui; Son, Jeong-Yu; Shin, Seohyun; Seo, Boram; Lee, Phil Ho Alkenylation of phosphacoumarins via aerobic oxidative Heck reactions and their synthetic application to fluorescent benzophosphacoumarins. Organic letters, 2015, 17, 908-911 |
| 1554756 | CIF | C26 H23 B F4 N2 O2 | P 1 21/c 1 | 12.2068; 13.731; 14.626 90; 99.027; 90 | 2421.1 | Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts. Organic letters, 2015, 17, 924-927 |
| 1554764 | CIF | C25 H20 B F4 N O | P 1 21/n 1 | 10.72; 18.331; 12.174 90; 110.527; 90 | 2240.4 | Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts. Organic letters, 2015, 17, 924-927 |
| 1554765 | CIF | C25 H21 B F4 N2 O2 | P 1 21/c 1 | 12.3471; 13.3272; 13.9786 90; 98.588; 90 | 2274.42 | Luo, Ching-Zong; Jayakumar, Jayachandran; Gandeepan, Parthasarathy; Wu, Yun-Ching; Cheng, Chien-Hong Rhodium(III)-catalyzed vinylic C-H activation: a direct route toward pyridinium salts. Organic letters, 2015, 17, 924-927 |
| 1554767 | CIF | C31 H24 Cl N O3 | P 1 21 1 | 7.081; 19.406; 9.491 90; 98.161; 90 | 1290.99 | Jayakumar, Samydurai; Kumarswamyreddy, Nandarapu; Prakash, Muthuraj; Kesavan, Venkitasamy Palladium catalyzed asymmetric allylation of 3-OBoc-oxindoles: an efficient synthesis of 3-allyl-3-hydroxyoxindoles. Organic letters, 2015, 17, 1066-1069 |
| 1554773 | CIF | C49.05 H59.38 Cl5.87 Li0.15 N3 P3 Ti2 | P -1 | 10.3083; 14.3567; 19.2355 75.287; 74.747; 84.913 | 2655.7 | Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J. Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes. Organic letters, 2015, 17, 752-755 |
| 1554774 | CIF | C16 H19 Cl3 N P Ti | P -1 | 8.8951; 9.2936; 13.0036 79.226; 76.069; 64.74 | 939.24 | Walker, Whitney K.; Anderson, Diana L.; Stokes, Ryjul W.; Smith, Stacey J.; Michaelis, David J. Allylic aminations with hindered secondary amine nucleophiles catalyzed by heterobimetallic Pd-Ti complexes. Organic letters, 2015, 17, 752-755 |
| 1554776 | CIF | C35 H26 N1.6 O10 | P 21 21 21 | 13.871; 15.1622; 64.627 90; 90; 90 | 13592 | Cao, Pei; Yang, Jing; Miao, Cui-Ping; Yan, Yijun; Ma, Ya-Tuan; Li, Xiao-Nian; Zhao, Li-Xing; Huang, Sheng-Xiong New duclauxamide from Penicillium manginii YIM PH30375 and structure revision of the duclauxin family. Organic letters, 2015, 17, 1146-1149 |
| 1554782 | CIF | C34 H29 N5 O4 S | P -1 | 9.7972; 10.509; 15.4371 72.931; 74.564; 84.268 | 1464.2 | Du, Zao; Xing, Yanpeng; Lu, Ping; Wang, Yanguang Copper-catalyzed cascade double C3-indolations of 3-diazoindolin-2-imines with indoles: convenient access to 3,3-diaryl-2-iminoindoles. Organic letters, 2015, 17, 1192-1195 |
| 1554783 | CIF | C24 H27 N3 O2 | P 1 21/c 1 | 17.5333; 9.245; 13.3467 90; 107.946; 90 | 2058.18 | Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides. Organic letters, 2015, 17, 1184-1187 |
| 1554791 | CIF | C21 H15 N3 O | P 1 21/c 1 | 10.5706; 17.3802; 10.1316 90; 96.996; 90 | 1847.5 | Bechara, William S.; Khazhieva, Inna S.; Rodriguez, Elsa; Charette, André B One-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles via the addition of hydrazides to activated secondary amides. Organic letters, 2015, 17, 1184-1187 |
| 1554793 | CIF | C24 H21 I N2 O3 S | P 21 21 21 | 10.7482; 12.7229; 16.152 90; 90; 90 | 2208.76 | Fu, Shaomin; Yang, Honghao; Li, Guoqiang; Deng, Yuanfu; Jiang, Huanfeng; Zeng, Wei Copper(II)-catalyzed enantioselective intramolecular cyclization of N-alkenylureas. Organic letters, 2015, 17, 1018-1021 |
| 1554794 | CIF | C19 H24 N2 O | P c a 21 | 12.8993; 10.853; 11.6466 90; 90; 90 | 1630.5 | Li, Bo; Wang, Si-Qing; Liu, Bin; Shi, Bing-Feng Synthesis of oxazolines from amides via palladium-catalyzed functionalization of unactivated C(sp(3))-H bond. Organic letters, 2015, 17, 1200-1203 |
| 1554796 | CIF | C24 H44 B2 N2 O4 | P b a m | 12.939; 13.093; 15.573 90; 90; 90 | 2638.2 | Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water. Organic letters, 2015, 17, 1212-1215 |
| 1554797 | CIF | C29 H49 B2 Co N2 O4 | F d d 2 | 18.923; 58.36; 11.127 90; 90; 90 | 12288 | Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water. Organic letters, 2015, 17, 1212-1215 |
| 1554798 | CIF | C24 H46 B2 N2 O5 | P 1 21/n 1 | 10.74; 19.626; 13.066 90; 93.197; 90 | 2749.8 | Onuma, Kaoru; Suzuki, Katsunori; Yamashita, Makoto Rhombic cyclobutadiene with a boryl/amino-substitution pattern: boryl group migration induced by reaction with water. Organic letters, 2015, 17, 1212-1215 |
| 1554802 | CIF | C24 H41 B2 O2 P | P 1 21/n 1 | 8.6014; 17.6656; 16.4517 90; 107.162; 90 | 2388.51 | Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes. Organic letters, 2015, 17, 1216-1219 |
| 1554803 | CIF | C28 H33 B2 Fe O2 P | P 1 21 1 | 12.674; 9.2986; 12.919 90; 113.497; 90 | 1396.3 | Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes. Organic letters, 2015, 17, 1216-1219 |
| 1554804 | CIF | C40 H43 B2 Fe P | P 21 21 21 | 10.3874; 17.4963; 18.3521 90; 90; 90 | 3335.3 | Bayardon, Jérôme; Bernard, Julie; Rémond, Emmanuelle; Rousselin, Yoann; Malacea-Kabbara, Raluca; Jugé, Sylvain Efficient synthesis of (P-chirogenic) o-boronated phosphines from sec-phosphine boranes. Organic letters, 2015, 17, 1216-1219 |
| 1554806 | CIF | C13 H12 O4 | P 1 21/n 1 | 10.5408; 14.0223; 15.567 90; 95.216; 90 | 2291.4 | Wang, Hong-Li; Shang, Ming; Sun, Shang-Zheng; Zhou, Zeng-Le; Laforteza, Brian N.; Dai, Hui-Xiong; Yu, Jin-Quan Cu(II)-catalyzed coupling of aromatic C-H bonds with malonates. Organic letters, 2015, 17, 1228-1231 |
| 1554809 | CIF | C19 H18 N O5 S2 | P -1 | 7.9459; 8.3713; 15.0845 98.477; 91.135; 97.754 | 982.54 | Deng, Zhimin; Wei, Jialiang; Liao, Lihao; Huang, Haiyan; Zhao, Xiaodan Organoselenium-catalyzed, hydroxy-controlled regio- and stereoselective amination of terminal alkenes: efficient synthesis of 3-amino allylic alcohols. Organic letters, 2015, 17, 1834-1837 |
| 1554810 | CIF | C24 H22 O3 | C 1 c 1 | 14.8194; 23.1341; 17.3079 90; 104.994; 90 | 5731.7 | Gelat, Fabien; Richard, Vincent; Berger, Olivier; Montchamp, Jean-Luc Development of a new family of chiral auxiliaries. Organic letters, 2015, 17, 1819-1821 |
| 1554813 | CIF | C17 H16 Cl N3 O | P -1 | 8.6811; 13.1015; 15.2298 66.74; 82.416; 77.876 | 1553.57 | Guo, Xiao; Chen, Wenteng; Chen, Binhui; Huang, Wei; Qi, Weixing; Zhang, Guolin; Yu, Yongping One-pot three-component strategy for functionalized 2-aminoimidazoles via ring opening of α-nitro epoxides. Organic letters, 2015, 17, 1157-1159 |
| 1554814 | CIF | C34 H35 N O6 S | P 21 21 21 | 9.4387; 22.551; 28.131 90; 90; 90 | 5987.7 | Peng, Peng; Geng, Yiqun; Göttker-Schnetmann, Inigo; Schmidt, Richard R. 2-Nitro-thioglycosides: α- and β-selective generation and their potential as β-selective glycosyl donors. Organic letters, 2015, 17, 1421-1424 |
| 1554815 | CIF | C19 H21 F2 N O | P 1 21/c 1 | 9.9286; 17.0093; 10.0841 90; 90.259; 90 | 1703 | He, Zhengbiao; Tan, Ping; Ni, Chuanfa; Hu, Jinbo Fluoroalkylative aryl migration of conjugated N-arylsulfonylated amides using easily accessible sodium di- and monofluoroalkanesulfinates. Organic letters, 2015, 17, 1838-1841 |
| 1554822 | CIF | C16 H10 N2 O | P 1 21/n 1 | 6.4176; 20.0965; 9.335 90; 98.274; 90 | 1191.42 | Chen, Xiaopei; Cui, Xiuling; Yang, Fangfang; Wu, Yangjie Base-promoted cross-dehydrogenative coupling of quinoline N-oxides with 1,3-azoles. Organic letters, 2015, 17, 1445-1448 |
| 1554824 | CIF | C20 H14 O5 | P 1 21/n 1 | 9.0391; 9.7069; 17.2285 90; 102.573; 90 | 1475.41 | Tian, Yuan; Jiang, Nan; Zhang, Ai Hua; Chen, Chao Jun; Deng, Xin Zhao; Zhang, Wen Jing; Tan, Ren Xiang Muta-mycosynthesis of naphthalene analogs. Organic letters, 2015, 17, 1457-1460 |
| 1554830 | CIF | C20 H25 F3 N2 O3 S | P 1 21/c 1 | 8.128; 15.344; 16.979 90; 102.44; 90 | 2067.8 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554831 | CIF | C22 H30 F3 N3 O3 S | C 1 2/c 1 | 15.441; 10.924; 27.769 90; 90.9; 90 | 4683.4 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554832 | CIF | C18 H22 F3 N3 O3 S | P 1 21/c 1 | 8.4815; 11.074; 21.3223 90; 93.426; 90 | 1999.1 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554833 | CIF | C21 H25 N3 | P -1 | 8.61; 9.179; 11.835 93.38; 95.73; 105.2 | 894.57 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554834 | CIF | C20 H26 N2 | P 1 21/c 1 | 8.693; 17.464; 11.525 90; 103.69; 90 | 1700 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554835 | CIF | C14 H22 N2 | R 3 c :H | 26.3163; 26.3163; 10.403 90; 90; 120 | 6239.3 | van Dijk, Tom; Bakker, Martijn S.; Holtrop, Flip; Nieger, Martin; Slootweg, J. Chris; Lammertsma, Koop Base-stabilized nitrilium ions as convenient imine synthons. Organic letters, 2015, 17, 1461-1464 |
| 1554837 | CIF | C49 H29 B F20 N O2 Rh | P 1 21/c 1 | 12.2787; 24.2002; 15.5541 90; 101.818; 90 | 4523.9 | Otley, Kate D.; Ellman, Jonathan A. An efficient method for the preparation of styrene derivatives via Rh(III)-catalyzed direct C-H vinylation. Organic letters, 2015, 17, 1332-1335 |
| 1554838 | CIF | C18 H18 O2 | P 1 21/c 1 | 14.026; 8.7035; 12.0599 90; 104.008; 90 | 1428.4 | Liu, Rui; Lu, Ze-Hai; Hu, Xiao-Hui; Li, Jun-Li; Yang, Xian-Jin Monocarboxylation and intramolecular coupling of butenylated arenes via palladium-catalyzed C-H activation process. Organic letters, 2015, 17, 1489-1492 |
| 1554839 | CIF | C17 H16 O2 Se | P 1 21 1 | 6.9078; 10.3981; 10.0732 90; 95.471; 90 | 720.24 | Niu, Wenxue; Yeung, Ying-Yeung Catalytic and highly enantioselective selenolactonization. Organic letters, 2015, 17, 1660-1663 |
| 1554840 | CIF | C12 H20 O4 | P 32 | 13.594; 13.594; 5.7493 90; 90; 120 | 920.11 | Wang, Hengbin; Negretti, Solymar; Knauff, Allison R.; Montgomery, John Exo-selective reductive macrocyclization of ynals. Organic letters, 2015, 17, 1493-1496 |
| 1554841 | CIF | C14 H15 Br N2 O2 | P 21 21 21 | 9.2455; 10.1411; 14.412 90; 90; 90 | 1351.3 | Gu, Xiaodong; Dai, Yuanyuan; Guo, Tingting; Franchino, Allegra; Dixon, Darren J.; Ye, Jinxing A general, scalable, organocatalytic nitro-Michael addition to enones: enantioselective access to all-carbon quaternary stereocenters. Organic letters, 2015, 17, 1505-1508 |
| 1554842 | CIF | C22 H18 F N3 O2 S | P 1 21/c 1 | 15.7629; 11.6907; 10.7408 90; 100.958; 90 | 1943.22 | Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng Iâ‚‚-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles. Organic letters, 2015, 17, 1521-1524 |
| 1554855 | CIF | C18 H21 N3 O2 S2 | P 1 21/c 1 | 10.0095; 11.563; 16.5773 90; 99.859; 90 | 1890.32 | Senadi, Gopal Chandru; Hu, Wan-Ping; Lu, Ting-Yi; Garkhedkar, Amol Milind; Vandavasi, Jaya Kishore; Wang, Jeh-Jeng Iâ‚‚-TBHP-catalyzed oxidative cross-coupling of N-sulfonyl hydrazones and isocyanides to 5-aminopyrazoles. Organic letters, 2015, 17, 1521-1524 |
| 1554856 | CIF | C20 H26 N2 O8 Si | C 1 2/c 1 | 18.687; 6.709; 37.603 90; 90.534; 90 | 4714 | Yin, Zhiping; Liu, Zengjin; Huang, Zhenggang; Chu, Yang; Chu, Zhiwen; Hu, Jia; Gao, Lu; Song, Zhenlei Synthesis of functionalized γ-lactone via Sakurai exo-cyclization/rearrangement of 3,3-bis(silyl) enol ester with a tethered acetal. Organic letters, 2015, 17, 1553-1556 |
| 1554858 | CIF | C60 H85 I3 N10 O12 | P -1 | 14.2686; 14.6629; 17.0163 80.443; 70.781; 82.037 | 3301.6 | Saha, Subrata; Santra, Saikat; Ghosh, Pradyut [2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation. Organic letters, 2015, 17, 1854-1857 |
| 1554860 | CIF | C60 H78 Cl6 N10 O10 | C 1 2/c 1 | 22.9779; 30.564; 22.926 90; 114.207; 90 | 14685.1 | Saha, Subrata; Santra, Saikat; Ghosh, Pradyut [2]Pseudorotaxane composed of heteroditopic macrobicycle and pyridine N-oxide based axle: recognition site dependent axle orientation. Organic letters, 2015, 17, 1854-1857 |
| 1554862 | CIF | C27 H27 F3 N2 O8 | P -1 | 8.5362; 11.0883; 14.8339 89.337; 75.808; 89.011 | 1360.96 | Huang, Lin; Zheng, Sheng-Cai; Tan, Bin; Liu, Xin-Yuan Metal-free direct 1,6- and 1,2-difunctionalization triggered by radical trifluoromethylation of alkenes. Organic letters, 2015, 17, 1589-1592 |
| 1554864 | CIF | C14 H11 N O7 | P n a 21 | 8.6933; 19.9383; 7.6281 90; 90; 90 | 1322.18 | Dorfner, Walter L.; Carroll, Patrick J.; Schelter, Eric J. Substituted quinoline quinones as surrogates for the PQQ cofactor: an electrochemical and computational study. Organic letters, 2015, 17, 1850-1853 |
| 1554867 | CIF | C23 H26 Br N O4 S | P 1 21 1 | 9.8067; 9.9678; 11.8916 90; 104.237; 90 | 1126.7 | Serpier, Fabien; Flamme, Benjamin; Brayer, Jean-Louis; Folléas, Benoît; Darses, Sylvain Chiral pyrrolidines and piperidines from enantioselective rhodium-catalyzed cascade arylative cyclization. Organic letters, 2015, 17, 1720-1723 |
| 1554869 | CIF | C28 H19 N O3 S2 | P -1 | 10.443; 11.228; 11.795 70.186; 87.728; 65.484 | 1175.6 | Ming, Wenbo; Liu, Xiaocui; Wang, Lianjie; Liu, Jun; Wang, Mang Tandem Thien- and benzannulations of α-alkenoyl-α-alkynyl ketene dithioacetals with cyanoacetates: synthesis of functionalized benzo[b]thiophenes. Organic letters, 2015, 17, 1746-1749 |
| 1554871 | CIF | C15 H21 N O3 | P 1 21/n 1 | 5.1627; 14.8595; 17.7219 90; 96.198; 90 | 1351.59 | Borrero, Nicholas V.; DeRatt, Lindsey G.; Ferreira Barbosa, Lais; Abboud, Khalil A.; Aponick, Aaron Tandem gold-catalyzed dehydrative cyclization/diels-alder reactions: facile access to indolocarbazole alkaloids. Organic letters, 2015, 17, 1754-1757 |
| 1554873 | CIF | C20 H16 O2 | P 21 21 21 | 5.9724; 14.8969; 16.4863 90; 90; 90 | 1466.79 | Peraino, Nicholas J.; Wheeler, Kraig A.; Kerrigan, Nessan J. Diastereoselective synthesis of γ-lactones through reaction of enediolates with α,β-unsaturated sulfoxonium salts. Organic letters, 2015, 17, 1735-1737 |
| 1554875 | CIF | C12 H13 Br O2 | P 1 21/c 1 | 6.0066; 11.7969; 16.772 90; 97.594; 90 | 1178 | Che, Chao; Zheng, Hanliang; Zhu, Gangguo Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides. Organic letters, 2015, 17, 1617-1620 |
| 1554877 | CIF | C23 H21 N | P 1 21/c 1 | 10.4176; 11.9596; 16.0413 90; 114.231; 90 | 1822.51 | Che, Chao; Zheng, Hanliang; Zhu, Gangguo Copper-catalyzed trans-carbohalogenation of terminal alkynes with functionalized tertiary alkyl halides. Organic letters, 2015, 17, 1617-1620 |
| 1554878 | CIF | C29 H36 N2 O4 | P 1 21 1 | 8.527; 16.7982; 9.3056 90; 102.717; 90 | 1300.22 | Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates. Organic letters, 2015, 17, 2054-2057 |
| 1554880 | CIF | C13 H22 O2 | C 1 c 1 | 14.0887; 10.5929; 9.0247 90; 114.771; 90 | 1222.92 | Prado, Gustavo; Veiga, Alberte X.; Fernández-Nieto, Fernando; Paleo, M. Rita; Sardina, F. Javier A two-step, stereoselective synthesis of nine- and ten-membered carbocycles from phthalates. Organic letters, 2015, 17, 2054-2057 |
| 1554885 | CIF | C20 H20 Br2 Cl2 N2 O4 | P 1 | 5.0746; 14.828; 16.699 65.191; 89.579; 80.838 | 1123.5 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554887 | CIF | C13 H15 Br Cl N O3 | P 1 21 1 | 4.8035; 8.2644; 18.363 90; 94.441; 90 | 726.79 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554890 | CIF | C13 H16 Br Cl2 N O3 | P 1 21 1 | 10.669; 4.7706; 15.964 90; 107.952; 90 | 773 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554894 | CIF | C6 H12 Cl2 O2 | P 1 21 1 | 4.9886; 19.578; 9.0155 90; 92.03; 90 | 880 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554896 | CIF | C13 H15 Br Cl N O3 | P 1 21 1 | 12.2792; 4.9357; 13.4763 90; 115.38; 90 | 737.92 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554898 | CIF | C13 H15 Br Cl N O3 | C 1 2 1 | 16.929; 4.841; 36.446 90; 101.211; 90 | 2930 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554900 | CIF | C14 H18 Cl N O8 S | P 21 21 21 | 6.1403; 13.657; 20.719 90; 90; 90 | 1737.5 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554902 | CIF | C6 H12 Cl2 O2 | P 21 21 21 | 5.8932; 9.8358; 14.7998 90; 90; 90 | 857.86 | Shemet, Andrej; Sarlah, David; Carreira, Erick M. Stereochemical studies of the opening of chloro vinyl epoxides: cyclic chloronium ions as intermediates. Organic letters, 2015, 17, 1878-1881 |
| 1554904 | CIF | C18 H14 N2 O | P 1 21/c 1 | 17.283; 5.72; 16.0086 90; 115.367; 90 | 1430 | Bunescu, Ala; Wang, Qian; Zhu, Jieping Synthesis of functionalized epoxides by copper-catalyzed alkylative epoxidation of allylic alcohols with alkyl nitriles. Organic letters, 2015, 17, 1890-1893 |
| 1554907 | CIF | C28 H36 N2 O10 Pd3 | P 1 21/c 1 | 8.2684; 13.1049; 14.9823 90; 98.209; 90 | 1606.8 | Guo, Kun; Chen, Xiaolan; Guan, Mingyu; Zhao, Yingsheng Direct ortho-C-H functionalization of aromatic alcohols masked by acetone oxime ether via exo-palladacycle. Organic letters, 2015, 17, 1802-1805 |
| 1554909 | CIF | C21 H24 B N O2 | P 1 21/n 1 | 9.82013; 15.1033; 12.9881 90; 93.8267; 90 | 1922.05 | Pareek, Manish; Fallon, Thomas; Oestreich, Martin Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling. Organic letters, 2015, 17, 2082-2085 |
| 1554912 | CIF | C20 H41 B2 F8 N5 O | P 21 21 21 | 9.9728; 10.8425; 25.575 90; 90; 90 | 2765.4 | Mirabdolbaghi, Roya; Dudding, Travis Expanding the forefront of strong organic Brønsted acids: proton-catalyzed hydroamination of unactivated alkenes and activation of Au(I) for alkyne hydroamination. Organic letters, 2015, 17, 1930-1933 |
| 1554914 | CIF | C25 H36 F3 N3 O4 | P -1 | 7.9555; 12.7291; 14.1773 101.894; 105.578; 101.34 | 1304 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554915 | CIF | C20 H27 F3 N2 O3 | P 1 21/c 1 | 9.676; 6.0187; 35.338 90; 90.313; 90 | 2057.9 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554916 | CIF | C18 H23 F3 N2 O3 | P -1 | 8.4082; 8.9935; 12.6932 109.241; 90.111; 102.16 | 883.25 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554917 | CIF | C18 H16 F3 N O | P 21 21 21 | 5.8836; 19.2027; 26.5181 90; 90; 90 | 2996 | Geoghegan, Kimberly; Bode, Jeffrey W. Bespoke SnAP reagents for the synthesis of C-substituted spirocyclic and bicyclic saturated N-heterocycles. Organic letters, 2015, 17, 1934-1937 |
| 1554920 | CIF | C21 H16 N2 O2 S | C 1 c 1 | 13.529; 16.7566; 8.6938 90; 116.175; 90 | 1768.8 | Lee, Dong Jin; Yoo, Eun Jeong Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions. Organic letters, 2015, 17, 1830-1833 |
| 1554921 | CIF | C24 H24 N2 O2 S | P 1 21/c 1 | 12.5268; 10.8502; 16.3904 90; 103.482; 90 | 2166.4 | Lee, Dong Jin; Yoo, Eun Jeong Efficient synthesis of C-N-coupled heterobiaryls by sequential N-H functionalization reactions. Organic letters, 2015, 17, 1830-1833 |
| 1554924 | CIF | C19 H29 F N2 O5 Si | P 21 21 21 | 6.42; 8.0707; 40.1927 90; 90; 90 | 2082.54 | Istrate, Alena; Medvecky, Michal; Leumann, Christian J. 2'-Fluorination of tricyclo-DNA controls furanose conformation and increases RNA affinity. Organic letters, 2015, 17, 1950-1953 |
| 1554926 | CIF | C19 H16 N2 O4 | P 1 21 1 | 7.5248; 11.7969; 18.7512 90; 98.035; 90 | 1648.2 | Bisai, Vishnumaya; Unhale, Rajshekhar A.; Suneja, Arun; Dhanasekaran, Sivasankaran; Singh, Vinod K. An Efficient Entry to syn- and anti-Selective Isoindolinones via an Organocatalytic Direct Mannich/Lactamization Sequence. Organic letters, 2015, 17, 2102-2105 |
| 1554930 | CIF | C16 H25 N O2 S3 | P 21 21 21 | 5.36225; 12.0412; 27.5363 90; 90; 90 | 1777.96 | Das, Manas; O'Shea, Donal F Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines. Organic letters, 2015, 17, 1962-1965 |
| 1554932 | CIF | C18 H19 Cl F3 N O S | P 1 21 1 | 11.7646; 15.4251; 12.0356 90; 118.452; 90 | 1920.3 | Das, Manas; O'Shea, Donal F Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines. Organic letters, 2015, 17, 1962-1965 |
| 1554934 | CIF | C19 H23 Fe N O2 S | P 1 21 1 | 5.84461; 11.3132; 13.829 90; 95.4227; 90 | 910.298 | Das, Manas; O'Shea, Donal F Silyloxide-promoted diastereoselective addition of aryl and heterocyclic trimethylsilanes to N-tert-butanesulfinylimines. Organic letters, 2015, 17, 1962-1965 |
| 1554935 | CIF | C23 H17 Cl O2 | P 1 21/m 1 | 9.353; 7.448; 12.251 90; 93.725; 90 | 851.6 | Liu, Yang; Jin, Shiyu; Huang, Liping; Hu, Youhong Phase transfer reagent promoted tandem ring-opening and ring-closing reactions of unique 3-(1-alkynyl) chromones. Organic letters, 2015, 17, 2134-2137 |
| 1554937 | CIF | C133 H116 N8 O21 S4 | P 1 21 1 | 10.8299; 17.8426; 16.7462 90; 105.418; 90 | 3119.5 | Xie, Danbo; Yang, Limin; Lin, Youqiang; Zhang, Zhiming; Chen, Dongdong; Zeng, Xiaofei; Zhong, Guofu Rapid access to spirocylic oxindoles: application of asymmetric N-heterocyclic carbene-catalyzed [3 + 3] cycloaddition of imines to oxindole-derived enals. Organic letters, 2015, 17, 2318-2321 |
| 1554941 | CIF | C39 H30 Cl N O | P 1 21/n 1 | 14.7817; 10.4931; 20.1054 90; 110.04; 90 | 2929.66 | Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H. Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization. Organic letters, 2015, 17, 1986-1989 |
| 1554944 | CIF | C24 H24 Cl N O | P 1 21/n 1 | 12.0241; 10.8634; 15.0306 90; 92.829; 90 | 1960.94 | Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H. Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization. Organic letters, 2015, 17, 1986-1989 |
| 1554948 | CIF | C24 H24 Cl N O | P 1 21/c 1 | 16.3879; 7.0026; 17.8667 90; 103.718; 90 | 1991.86 | Koy, Maximilian; Engle, Keary M.; Henling, Lawrence M.; Takase, Michael K.; Grubbs, Robert H. Synthesis of substituted dihydrobenzofurans via tandem S(N)Ar/5-exo-trig cyclization. Organic letters, 2015, 17, 1986-1989 |
| 1554950 | CIF | C152.5 H199 B4 N7 O23 | P 1 21/c 1 | 11.705; 28.512; 22.406 90; 98.94; 90 | 7387 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554955 | CIF | C50 H44 F24 N4 P4 | P 1 21/n 1 | 13.488; 14.281; 14.287 90; 108.36; 90 | 2611.9 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554956 | CIF | C186 H168 B4 N14 O31 | P -1 | 16.134; 16.609; 16.766 85.82; 65.15; 75.26 | 3939.7 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554959 | CIF | C117 H171 B4 N4 O20 | P 1 21/c 1 | 42.193; 8.356; 15.63 90; 90.76; 90 | 5510.1 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554960 | CIF | C180 H112 B4 D84 N4 O34 S14 | P -1 | 16.67; 17.44; 19.659 81.21; 74.06; 62.19 | 4859 | Danjo, Hiroshi; Hashimoto, Yuhki; Kidena, Yuki; Nogamine, Ayumi; Katagiri, Kosuke; Kawahata, Masatoshi; Miyazawa, Toshifumi; Yamaguchi, Kentaro Nestable Tetrakis(spiroborate) Nanocycles. Organic letters, 2015, 17, 2154-2157 |
| 1554968 | CIF | C70 H56 N8 O8 | P -1 | 11.446; 13.451; 22.036 98.71; 104.3; 98.36 | 3189.9 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554969 | CIF | C32 H26 N4 O2 | C 1 2/c 1 | 16.098; 8.0852; 19.417 90; 103.12; 90 | 2461.3 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554971 | CIF | C34 H30 N4 O4 | P 1 21/c 1 | 7.3964; 23.302; 16.073 90; 94.05; 90 | 2763.3 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554973 | CIF | C70 H58 Cl6 N8 O12 S | C 1 c 1 | 37.78; 8.9173; 26.953 90; 133.41; 90 | 6596 | Anguera, Gonzalo; Kauffmann, Brice; Borrell, José I; Borrós, Salvador; Sánchez-García, David Quaterpyrroles as building blocks for the synthesis of expanded porphyrins. Organic letters, 2015, 17, 2194-2197 |
| 1554978 | CIF | C16 H10 Br N O4 | P 1 21/c 1 | 12.4447; 15.6502; 7.9646 90; 105.739; 90 | 1493 | Bag, Raghunath; Sar, Dinabandhu; Punniyamurthy, Tharmalingam Copper(II)-catalyzed direct dioxygenation of alkenes with air and N-hydroxyphthalimide: synthesis of β-keto-N-alkoxyphthalimides. Organic letters, 2015, 17, 2010-2013 |
| 1554981 | CIF | C70 H120 N14 O26 S8 | P -1 | 13.0106; 13.1402; 14.3888 80.344; 63.999; 78.993 | 2160.42 | Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail New "pyrene box" cages for adaptive guest conformations. Organic letters, 2015, 17, 2178-2181 |
| 1554982 | CIF | C30 H60 N12 O16 S4 | C 1 2/c 1 | 13.4741; 14.6965; 22.6791 90; 92.704; 90 | 4485.96 | Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail New "pyrene box" cages for adaptive guest conformations. Organic letters, 2015, 17, 2178-2181 |
| 1554988 | CIF | C40 H69.97 N4 O14 S4 | P -1 | 11.2634; 15.966; 16.009 111.587; 100.691; 109.004 | 2373.6 | Dumitrescu, Dan; Dumitru, Florina; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail New "pyrene box" cages for adaptive guest conformations. Organic letters, 2015, 17, 2178-2181 |
| 1554990 | CIF | C15 H13 N O4 S | P 21 21 21 | 8.1609; 9.0398; 19.318 90; 90; 90 | 1425.1 | Liu, Yan-Kai; Li, Zhi-Long; Li, Ji-Yao; Feng, Huan-Xi; Tong, Zhi-Ping Open-close: an alternative strategy to α-functionalization of lactone via enamine catalysis in one pot under mild conditions. Organic letters, 2015, 17, 2022-2025 |
| 1554994 | CIF | C28 H23 N3 O4 S | P 1 21/n 1 | 12.8623; 11.3355; 16.9579 90; 94.493; 90 | 2464.87 | Chen, Jing; Li, Jianjun; Wang, Jiazhe; Li, Hao; Wang, Wei; Guo, Yuewei Phosphine-Catalyzed Aza-MBH Reactions of Vinylpyridines: Efficient and Rapid Access to 2,3,5-Triarylsubstituted 3-Pyrrolines. Organic letters, 2015, 17, 2214-2217 |
| 1554996 | CIF | C19 H22 O7 | P 1 21/n 1 | 6.0808; 23.3393; 12.5225 90; 94.028; 90 | 1772.82 | Tan, Ceheng; Chen, Wei; Mu, Xinpeng; Chen, Qi; Gong, Jianxian; Luo, Tuoping; Yang, Zhen Synthetic Progress toward Azadirachtins. 2. Enantio- and Diastereoselective Synthesis of the Right-Wing Fragment of 11-epi-Azadirachtin I. Organic letters, 2015, 17, 2338-2341 |
| 1554998 | CIF | C26 H31 Br N2 O3 | P -1 | 9.6121; 11.761; 13.648 98.331; 109.571; 113.637 | 1260.2 | Zeng, Xiao-Hua; Wang, Hong-Mei; Ding, Ming-Wu Unexpected Synthesis of 5,6-Dihydropyridin-2(1H)-ones by a Domino Ugi/Aldol/Hydrolysis Reaction Starting from Baylis-Hillman Phosphonium Salts. Organic letters, 2015, 17, 2234-2237 |
| 1555000 | CIF | C38 H44 B2 F4 N4 O6 | P -1 | 9.7881; 13.2333; 16.5195 67.596; 77.669; 72.069 | 1870.86 | Huaulmé, Quentin; Mirloup, Antoine; Retailleau, Pascal; Ziessel, Raymond Synthesis of Highly Functionalized BOPHY Chromophores Displaying Large Stokes Shifts. Organic letters, 2015, 17, 2246-2249 |
| 1555003 | CIF | C27 H30 F N O2 | P -1 | 9.3088; 9.5092; 14.5742 92.724; 104.673; 110 | 1159.92 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555004 | CIF | C28 H32 F N O2 | P 21 21 21 | 8.03153; 10.686; 28.3689 90; 90; 90 | 2434.76 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555005 | CIF | C28 H32 N4 O2 | P 32 2 1 | 11.32263; 11.32263; 35.383 90; 90; 120 | 3928.44 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555006 | CIF | C30 H35 N O4 | P 1 | 9.7073; 10.168; 14.0374 85.597; 85.998; 82.306 | 1366.53 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555007 | CIF | C28 H31 F2 N O2 | P 1 | 10.4764; 10.6867; 12.3768 85.757; 70.552; 69.477 | 1222.26 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555008 | CIF | C28 H31 F2 N O2 | P 1 21 1 | 7.90952; 16.3522; 9.53794 90; 95.6737; 90 | 1227.58 | Davies, Stephen G.; Fletcher, Ai M.; Frost, Aileen B.; Roberts, Paul M.; Thomson, James E. Asymmetric Synthesis of Substituted anti-β-Fluorophenylalanines. Organic letters, 2015, 17, 2254-2257 |
| 1555011 | CIF | C23 H27 Br N2 O5 | P 1 21/n 1 | 8.3956; 11.6027; 23.715 90; 91.1454; 90 | 2309.7 | Arai, Takayoshi; Tsuchiya, Kento; Matsumura, Eri PyBidine-NiCl2-Catalyzed Asymmetric Addition of Alcohols and Peroxides to Isatin-Derived Ketimines. Organic letters, 2015, 17, 2416-2419 |
| 1555012 | CIF | C8 H11 F3 N2 O S | P 1 21/c 1 | 8.4044; 11.3774; 11.5451 90; 96.16; 90 | 1097.6 | Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng Copper-Catalyzed Intermolecular Trifluoromethylthiocyanation of Alkenes: Convenient Access to CF3-Containing Alkyl Thiocyanates. Organic letters, 2015, 17, 2438-2441 |
| 1555018 | CIF | C76 H112 F14 N4 Sn4 | P -1 | 10.7975; 11.121; 17.986 82.945; 76.059; 70.925 | 1978.74 | Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H. Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives. Organic letters, 2015, 17, 2266-2269 |
| 1555019 | CIF | C32 H4 F26 N4 | P -1 | 6.15317; 9.3804; 13.8177 103.878; 100.265; 98.23 | 747.31 | Hahn, Lena; Wadepohl, Hubert; Gade, Lutz H. Tetralithiated tetraazaperopyrene as a key intermediate for the synthesis of functionalized derivatives. Organic letters, 2015, 17, 2266-2269 |
| 1555021 | CIF | C19 H18 O2 | P n a 21 | 12.91; 9.664; 12.157 90; 90; 90 | 1516.7 | Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J. Michael Additions of Highly Basic Enolates to ortho-Quinone Methides. Organic letters, 2015, 17, 2278-2281 |
| 1555022 | CIF | C17 H22 O2 | P 21 21 21 | 8.6511; 11.009; 15.784 90; 90; 90 | 1503.3 | Lewis, Robert S.; Garza, Christopher J.; Dang, Ann T.; Pedro, Te Kie A.; Chain, William J. Michael Additions of Highly Basic Enolates to ortho-Quinone Methides. Organic letters, 2015, 17, 2278-2281 |
| 1555026 | CIF | C22 H21 N O3 | P -1 | 9.724; 10.178; 10.676 62.165; 79.328; 69.089 | 872.6 | Capreti, Naylil M. R.; Jurberg, Igor D. Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: A Divergent Entry to β-Branched Carbonyl Compounds. Organic letters, 2015, 17, 2490-2493 |
| 1555028 | CIF | C15 H13 N O | R -3 :H | 26.4383; 26.4383; 8.6956 90; 90; 120 | 5263.8 | Zhang, Yan; Wang, Dahai; Cui, Sunliang Facile Synthesis of Isoindolinones via Rh(III)-Catalyzed One-Pot Reaction of Benzamides, Ketones, and Hydrazines. Organic letters, 2015, 17, 2494-2497 |
| 1555031 | CIF | C36 H39 N O2 | P 1 21/c 1 | 14.8225; 11.0736; 18.657 90; 100.056; 90 | 3015.3 | Reddy, Virsinha; Vijaya Anand, Ramasamy Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach. Organic letters, 2015, 17, 3390-3393 |
| 1555034 | CIF | C25 H27 Fe N O3 S | P 1 21 1 | 15.0789; 8.6357; 18.2167 90; 106.122; 90 | 2278.8 | Ogasawara, Masamichi; Wada, Shiro; Isshiki, Erika; Kamimura, Takumi; Yanagisawa, Akira; Takahashi, Tamotsu; Yoshida, Kazuhiro Enantioselective synthesis of planar-chiral ferrocene-fused 4-pyridones and their application in construction of pyridine-based organocatalyst library. Organic letters, 2015, 17, 2286-2289 |
| 1555037 | CIF | C17 H14 N2 O3 | P 1 21/c 1 | 8.9224; 9.3813; 18.2533 90; 103.064; 90 | 1488.32 | Son, Jeong-Yu; Kim, Sunghwa; Jeon, Woo Hyung; Lee, Phil Ho Synthesis of Cinnolin-3(2H)-one Derivatives from Rh-Catalyzed Reaction of Azobenzenes with Diazotized Meldrum's Acid. Organic letters, 2015, 17, 2518-2521 |
| 1555039 | CIF | C26 H28 O5 | P -1 | 10.896; 11.118; 11.442 109.812; 100.766; 111.223 | 1137.4 | Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products. Organic letters, 2015, 17, 3446-3449 |
| 1555041 | CIF | C23 H24 O3 | P -1 | 8.428; 11.011; 11.459 65.415; 87.993; 89.668 | 966.4 | Naresh, Gunaganti; Kant, Ruchir; Narender, Tadigoppula Silver(I)-Catalyzed Regioselective Construction of Highly Substituted α-Naphthols and Its Application toward Expeditious Synthesis of Lignan Natural Products. Organic letters, 2015, 17, 3446-3449 |
| 1555044 | CIF | C21 H36 O4 Si | C 1 2 1 | 22.265; 7.7011; 12.8529 90; 102.095; 90 | 2154.9 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555045 | CIF | C12 H14 O3 | P 1 21/c 1 | 12.324; 7.8713; 10.6532 90; 92.217; 90 | 1032.65 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555051 | CIF | C36 H55 N O7 Si2 | P -1 | 8.9128; 10.9914; 20.184 91.339; 96.624; 104.357 | 1899.99 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555052 | CIF | C15 H20 O5 | P 21 21 21 | 7.3936; 10.5735; 17.817 90; 90; 90 | 1392.9 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555053 | CIF | C21 H38 O5 S | P 1 21/c 1 | 16.4753; 10.1532; 13.8282 90; 98.669; 90 | 2286.71 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
| 1555059 | CIF | C15 H22 O6 | P 1 21/n 1 | 8.5281; 18.7862; 9.5185 90; 100.368; 90 | 1500.07 | Peng, Shao-Zheng; Sha, Chin-Kang Stereoselective Total Syntheses of Guanacastepenes N and O. Organic letters, 2015, 17, 3486-3489 |
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