Crystallography Open Database
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Searching journal of publication like 'The Journal of organic chemistry' volume of publication is 85
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 4038082 | CIF | C28 H28 Br N2 O5 S | P -1 | 8.3713; 12.9078; 13.4996 73.9; 73.965; 79.977 | 1339.4 | Han, Pan; Mao, Zhuo-Ya; Li, Ming; Si, Chang-Mei; Wei, Bang-Guo; Lin, Guo-Qiang Synthesis of Amide Enol Carbamates and Carbonates through Cu(OTf)<sub>2</sub>-Catalyzed Reactions of Ynamides with <i>t</i>-Butyl Carbamates/Carbonates. The Journal of organic chemistry, 2020, 85, 4740-4752 |
| 4038083 | CIF | C56 H88.2 Cl3 F0.9 N8 O9.1 | P 1 21/n 1 | 12.1056; 18.4895; 27.4703 90; 96.269; 90 | 6111.8 | Delecluse, Magalie; Colomban, Cédric; Chatelet, Bastien; Chevallier-Michaud, Sabine; Moraleda, Delphine; Dutasta, Jean-Pierre; Martinez, Alexandre Highly Selective Fluoride Recognition by a Small Tris-Urea Covalent Cage. The Journal of organic chemistry, 2020, 85, 4706-4711 |
| 4038084 | CIF | C23 H36 O6 | P 1 21/c 1 | 7.3636; 27.079; 11.2689 90; 95.314; 90 | 2237.3 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038085 | CIF | C27 H46 O5 Si | P -1 | 10.142; 11.29; 13.629 83.009; 73.442; 70.541 | 1409.8 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038086 | CIF | C27 H42 O7 | C 1 c 1 | 13.152; 16.857; 12.706 90; 107.727; 90 | 2683.2 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038087 | CIF | C25 H42 O5 Si | P -1 | 9.5936; 11.1608; 14.6705 69.414; 79.03; 68.15 | 1361.7 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038088 | CIF | C25 H38 O5 | P 1 21/c 1 | 13.878; 17.626; 20.717 90; 97.877; 90 | 5020 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038089 | CIF | C25 H40 O5 | P b c a | 11.6702; 18.6897; 21.5803 90; 90; 90 | 4706.93 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038090 | CIF | C25 H40 O6 | P 21 21 21 | 8.674; 11.5004; 23.904 90; 90; 90 | 2384.5 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038091 | CIF | C24 H42 O5 Si | P 1 21/c 1 | 8.2593; 28.326; 10.769 90; 90.695; 90 | 2519.3 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038092 | CIF | C7 H8 O3 | P b c a | 8.5906; 7.0884; 20.553 90; 90; 90 | 1251.5 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038093 | CIF | C15 H20 O3 | P 1 21/n 1 | 7.8382; 16.7731; 9.7678 90; 101.18; 90 | 1259.81 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038094 | CIF | C22 H30 O4 | P 1 21/c 1 | 13.1931; 9.645; 15.711 90; 98.127; 90 | 1979.11 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038095 | CIF | C27 H38 N2 O4 | C 1 2/c 1 | 32.983; 19.298; 31.32 90; 98.677; 90 | 19707 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038096 | CIF | C7 H12 O3 | P -1 | 5.9092; 7.1583; 9.1902 92.766; 105.442; 108.026 | 352.68 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038097 | CIF | C15 H18 O3 | P 1 21 1 | 13.0633; 7.8253; 13.0916 90; 106.413; 90 | 1283.74 | Tong, Guanghu; Ding, Zhengwei; Liu, Zhi; Ding, You-Song; Xu, Liang; Zhang, Hailong; Li, Pengfei Total Synthesis of Prostratin, a Bioactive Tigliane Diterpenoid: Access to Multi-Stereocenter Cyclohexanes from a Phenol. The Journal of organic chemistry, 2020, 85, 4813-4837 |
| 4038098 | CIF | C25 H35 F3 O6 Si | P 1 21 1 | 13.1127; 7.7038; 14.0568 90; 97.859; 90 | 1406.65 | Kim, Jae Hyun; Song, Yeonghun; Kim, Min Jung; Kim, Sanghee Asymmetric Total Synthesis of Inthomycins A, B, and C. The Journal of organic chemistry, 2020, 85, 4795-4806 |
| 4038108 | CIF | C14 H17 O6 P | P 21 21 21 | 6.1955; 13.6351; 17.2061 90; 90; 90 | 1453.51 | Hernández-Guerra, Daniel; Kennedy, Alan R.; León, Elisa I; Martín, Ángeles; Pérez-Martín, Inés; Rodríguez, María S; Suárez, Ernesto Synthetic Approaches to Phosphasugars (2-oxo-1,2-oxaphosphacyclanes) Using the Anomeric Alkoxyl Radical β-Fragmentation Reaction as the Key Step. The Journal of organic chemistry, 2020, 85, 4861-4880 |
| 4038109 | CIF | C24 H19 N O | P 1 21/c 1 | 12.5295; 6.114; 24.4215 90; 104.339; 90 | 1812.5 | Parveen, Naziya; Sekar, Govindasamy Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones. The Journal of organic chemistry, 2020, 85, 4682-4694 |
| 4038110 | CIF | C21 H19 N O3 | C 1 2/c 1 | 20.5819; 12.8776; 13.9465 90; 102.536; 90 | 3608.3 | Parveen, Naziya; Sekar, Govindasamy Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones. The Journal of organic chemistry, 2020, 85, 4682-4694 |
| 4038111 | CIF | C24 H19 N O2 | P 1 21/n 1 | 14.253; 8.2293; 16.3693 90; 98.613; 90 | 1898.34 | Parveen, Naziya; Sekar, Govindasamy Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones. The Journal of organic chemistry, 2020, 85, 4682-4694 |
| 4038112 | CIF | C23 H15 Cl O2 | P 1 c 1 | 9.7179; 12.4696; 7.5883 90; 106.874; 90 | 879.95 | Parveen, Naziya; Sekar, Govindasamy Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones. The Journal of organic chemistry, 2020, 85, 4682-4694 |
| 4038113 | CIF | C27 H25 N O4 | P 1 21/c 1 | 8.1334; 31.8582; 9.231 90; 110.33; 90 | 2242.9 | Parveen, Naziya; Sekar, Govindasamy Palladium Nanoparticle-Catalyzed Stereoselective Domino Synthesis of 3-Allylidene-2(3<i>H</i>)-oxindoles and 3-Allylidene-2(3<i>H</i>)-benzofuranones. The Journal of organic chemistry, 2020, 85, 4682-4694 |
| 4038114 | CIF | C15 H8 O2 S2 | P 1 21/n 1 | 9.424; 9.68; 13.829 90; 94.214; 90 | 1258.1 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038115 | CIF | C15 H8 O2 S2 | P n m a | 15.3775; 7.2583; 11.0501 90; 90; 90 | 1233.35 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038116 | CIF | C13 H8 O2 | P 1 21/n 1 | 9.559; 5.316; 17.355 90; 92.38; 90 | 881.1 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038117 | CIF | C13 H6 Cl2 O2 | C 1 2/m 1 | 13.357; 12.364; 7.308 90; 118.676; 90 | 1058.9 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038118 | CIF | C15 H8 O4 | P 1 21/n 1 | 9.217; 12.573; 9.542 90; 99.09; 90 | 1091.9 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038119 | CIF | C15 H8 O3 S | P 1 21/n 1 | 9.457; 9.423; 13.368 90; 90.586; 90 | 1191.2 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038120 | CIF | C21 H12 O4 | P 1 21/n 1 | 11.825; 17.04; 16.23 90; 109.86; 90 | 3076 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038121 | CIF | C23 H12 O4 | P n a 21 | 17.395; 9.112; 10.203 90; 90; 90 | 1617.2 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038122 | CIF | C25 H14 O4 | P 21 21 21 | 13.845; 13.921; 18.938 90; 90; 90 | 3650 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038123 | CIF | C33 H18 O4 | C 2 2 21 | 8.351; 21.414; 13.48 90; 90; 90 | 2410.6 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038124 | CIF | C34 H20 Cl2 O4 | P 21 21 21 | 5.3479; 17.257; 28.107 90; 90; 90 | 2594 | Wössner, Jan S; Esser, Birgit Spiroconjugated Donor-σ-Acceptor Charge-Transfer Dyes: Effect of the π-Subsystems on the Optoelectronic Properties. The Journal of organic chemistry, 2020, 85, 5048-5057 |
| 4038125 | CIF | C132 H204 Cl36 Cu12 N48 O49.66 | C 1 2/m 1 | 26.405; 29.054; 13.1898 90; 105.232; 90 | 9763.4 | Yepremyan, Akop; Mekhail, Magy A.; Niebuhr, Brian P.; Pota, Kristof; Sadagopan, Nishanth; Schwartz, Timothy M.; Green, Kayla N. Synthesis of 12-Membered Tetra-aza Macrocyclic Pyridinophanes Bearing Electron-Withdrawing Groups. The Journal of organic chemistry, 2020, 85, 4988-4998 |
| 4038126 | CIF | C13 H20 Cl2 F6 N4 O6 S2 | P 1 21/c 1 | 11.471; 7.8357; 24.225 90; 90.475; 90 | 2177.3 | Yepremyan, Akop; Mekhail, Magy A.; Niebuhr, Brian P.; Pota, Kristof; Sadagopan, Nishanth; Schwartz, Timothy M.; Green, Kayla N. Synthesis of 12-Membered Tetra-aza Macrocyclic Pyridinophanes Bearing Electron-Withdrawing Groups. The Journal of organic chemistry, 2020, 85, 4988-4998 |
| 4038127 | CIF | C17 H21 N O3 | P -1 | 8.3484; 8.596; 10.5662 94.799; 97.856; 97.882 | 739.98 | Rinaldi, Antonia; Langé, Vittoria; Scarpi, Dina; Occhiato, Ernesto G. One-Pot Access to 1,7a-Dihydro-1,3a-ethano-indene and 1,8a-Dihydro-1,3a-ethano-azulene Skeletons by a Sequential Gold(I)-Catalyzed Propargyl Claisen Rearrangement/Nazarov Cyclization/[4+2] Cycloaddition Reaction. The Journal of organic chemistry, 2020, 85, 5078-5086 |
| 4038128 | CIF | C29 H22 O2 | P 1 21/c 1 | 7.7659; 24.493; 11.05 90; 102.439; 90 | 2052.48 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038129 | CIF | C29 H22 S2 | P 1 21/c 1 | 7.63396; 24.8669; 11.3736 90; 102.352; 90 | 2109.1 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038130 | CIF | C33 H32 N2 | I 41/a :2 | 30.826; 30.826; 10.4869 90; 90; 90 | 9965.1 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038131 | CIF | C25 H12 O S2 | C 1 2/c 1 | 25.198; 8.1409; 17.1786 90; 105.547; 90 | 3395 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038132 | CIF | C29 H22 N2 O | P 1 21/c 1 | 4.8822; 24.2724; 18.1588 90; 111.851; 90 | 1997.27 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038133 | CIF | C59 H52 N4 O | I -4 | 28.0545; 28.0545; 5.2665 90; 90; 90 | 4145.03 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038134 | CIF | C118 H99 N9 | I -4 | 28.056; 28.056; 5.2757 90; 90; 90 | 4152.71 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038135 | CIF | C61 H54 N4 O | I -4 | 28.0572; 28.0572; 5.2734 90; 90; 90 | 4151.25 | Górski, Krzysztof; Mech-Piskorz, Justyna; Leśniewska, Barbara; Pietraszkiewicz, Oksana; Pietraszkiewicz, Marek Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes. The Journal of organic chemistry, 2020, 85, 4672-4681 |
| 4038187 | CIF | C14 H9 N3 O S | P b c a | 11.6638; 7.5007; 27.8059 90; 90; 90 | 2432.65 | Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles. The Journal of organic chemistry, 2020, 85, 5570-5579 |
| 4038188 | CIF | C24 H20 N4 O3 S | P b c a | 13.0311; 10.4176; 30.827 90; 90; 90 | 4184.9 | Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles. The Journal of organic chemistry, 2020, 85, 5570-5579 |
| 4038189 | CIF | C12 H13 N3 O S2 | P 1 21/c 1 | 10.0149; 15.6728; 8.2966 90; 102.539; 90 | 1271.19 | Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles. The Journal of organic chemistry, 2020, 85, 5570-5579 |
| 4038190 | CIF | C24 H26 N4 O3 Se | P 1 21/c 1 | 11.4655; 12.7451; 15.4702 90; 100.414; 90 | 2223.4 | Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles. The Journal of organic chemistry, 2020, 85, 5570-5579 |
| 4038191 | CIF | C25 H25 N5 O2 | P 1 21/c 1 | 15.4232; 6.0725; 24.6911 90; 102.638; 90 | 2256.5 | Chen, Jin-Yu; Selvaraju, Manikandan; Lin, Yen-Tzu; Dhole, Sandip; Lin, Chih-Yu; Sun, Chung-Ming Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles. The Journal of organic chemistry, 2020, 85, 5570-5579 |
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