Crystallography Open Database

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4038785 CIFC36 H28 N2 O6 SP 1 21/n 18.3197; 18.7648; 19.0758
90; 95.6621; 90
2963.5Sun, Quan-Shun; Sun, Jing; Pan, Liu-Na; Yan, Chao-Guo
Selective Construction of Diverse Polycyclic Spirooxindoles via a Three-Component Reaction of Cyclic Mercapto-Substituted β-Enamino Esters, Isatins, and Cyclic 1,3-Diketones.
The Journal of organic chemistry, 2020, 85, 12117-12127
4038786 CIFC35 H25 F N2 O6 SP n a 2115.1594; 13.7549; 14.4974
90; 90; 90
3022.9Sun, Quan-Shun; Sun, Jing; Pan, Liu-Na; Yan, Chao-Guo
Selective Construction of Diverse Polycyclic Spirooxindoles via a Three-Component Reaction of Cyclic Mercapto-Substituted β-Enamino Esters, Isatins, and Cyclic 1,3-Diketones.
The Journal of organic chemistry, 2020, 85, 12117-12127
4038787 CIFC16 H16 N2P b c a11.62377; 11.62379; 19.3359
90; 90; 90
2612.52Aksenov, Nicolai A.; Aksenov, Dmitrii A.; Skomorokhov, Anton A.; Prityko, Lidiya A.; Aksenov, Alexander V.; Griaznov, Georgii D.; Rubin, Michael
Synthesis of 2-(1<i>H</i>-Indol-2-yl)acetamides via Brønsted Acid-Assisted Cyclization Cascade.
The Journal of organic chemistry, 2020, 85, 12128-12146
4038788 CIFC22 H32 N2 O9 P2P 1 21/c 110.246; 21.331; 12.725
90; 113.59; 90
2548.7Shu, Zhihao; Zhou, Jianhui; Li, Junyou; Cheng, Yilang; Liu, Hong; Wang, Dechuan; Zhou, Yu
Rh(III)-Catalyzed Dual C-H Functionalization/Cyclization Cascade by a Removable Directing Group: A Method for Synthesis of Polycyclic Fused Pyrano[<i>de</i>]Isochromenes.
The Journal of organic chemistry, 2020, 85, 12097-12107
4038789 CIFC17 H22 O8 P2C 1 2/c 122.428; 8.079; 10.933
90; 101.949; 90
1938.1Shu, Zhihao; Zhou, Jianhui; Li, Junyou; Cheng, Yilang; Liu, Hong; Wang, Dechuan; Zhou, Yu
Rh(III)-Catalyzed Dual C-H Functionalization/Cyclization Cascade by a Removable Directing Group: A Method for Synthesis of Polycyclic Fused Pyrano[<i>de</i>]Isochromenes.
The Journal of organic chemistry, 2020, 85, 12097-12107
4038790 CIFC16 H15 O4 PP b c a13.6; 7.1637; 29.5605
90; 90; 90
2879.97Shu, Zhihao; Zhou, Jianhui; Li, Junyou; Cheng, Yilang; Liu, Hong; Wang, Dechuan; Zhou, Yu
Rh(III)-Catalyzed Dual C-H Functionalization/Cyclization Cascade by a Removable Directing Group: A Method for Synthesis of Polycyclic Fused Pyrano[<i>de</i>]Isochromenes.
The Journal of organic chemistry, 2020, 85, 12097-12107
4038791 CIFC39 H28 Br N O6 SP 41 21 223.9795; 23.9795; 13.6928
90; 90; 90
7873.58Yan, Juzhang; Li, Xiaoping; Chen, Yuzhen; Li, Ying; Chen, Weiwen; Zhan, Ruoting; Huang, Huicai
Organocatalytic 1,4-Addition of Azadienes with 3-Homoacyl Coumarins toward Highly Enantioenriched Benzofuran Coumarin Skeletons.
The Journal of organic chemistry, 2020, 85, 12175-12186
4038792 CIFC11 H9 N3 OP -17.073; 8.1167; 8.7016
86.895; 81.037; 71.308
467.42Wang, Jian; Li, Jiang-Hua; Guo, Yidong; Dong, Hongbo; Liu, Qiang; Yu, Xiao-Qi
TEMPO-Mediated C-H Amination of Benzoxazoles with N-Heterocycles.
The Journal of organic chemistry, 2020, 85, 12797-12803
4038793 CIFC47 H44 N4 OP 1 21 19.5514; 10.8418; 18.966
90; 102.372; 90
1918.4Selby, Joshua; Holzapfel, Marco; Lombe, Blaise Kimbadi; Schmidt, David; Krause, Ana-Maria; Würthner, Frank; Bringmann, Gerhard; Lambert, Christoph
Chiroptical Properties of Indolenine Squaraines with a Stereogenic Center at Close Proximity.
The Journal of organic chemistry, 2020, 85, 12227-12242
4038794 CIFC41 H48 N4 OP 1 21 112.5152; 8.1909; 18.3478
90; 109.467; 90
1773.3Selby, Joshua; Holzapfel, Marco; Lombe, Blaise Kimbadi; Schmidt, David; Krause, Ana-Maria; Würthner, Frank; Bringmann, Gerhard; Lambert, Christoph
Chiroptical Properties of Indolenine Squaraines with a Stereogenic Center at Close Proximity.
The Journal of organic chemistry, 2020, 85, 12227-12242
4038795 CIFC20 H21 F3 N2 O7P 21 21 217.13243; 12.32391; 29.4905
90; 90; 90
2592.2Li, Luyao; Yang, Tianxiao; Zhang, Tao; Zhu, Bo; Chang, Junbiao
Organocatalytic Asymmetric Tandem Cyclization/Michael Addition via Oxazol-5(2<i>H</i>)-One Formation: Access to Perfluoroalkyl-Containing <i>N</i>,<i>O</i>-Acetal Derivatives.
The Journal of organic chemistry, 2020, 85, 12294-12303
4038796 CIFC15 H18 O S2P 1 21 18.4921; 11.0952; 8.7511
90; 118.324; 90
725.83Wang, Panpan; Jiang, Qian; Zhao, Ruibo; Xie, Xingang; Tang, Shouchu; Wang, Xiaolei
Enantioselective α-Functionalization of 1,3-Dithianes by Iridium-Catalyzed Allylic Substitution.
The Journal of organic chemistry, 2020, 85, 12456-12467
4038797 CIFC9 H14 O2 S2P 1 21 111.774; 6.7993; 13.767
90; 101.189; 90
1081.2Wang, Panpan; Jiang, Qian; Zhao, Ruibo; Xie, Xingang; Tang, Shouchu; Wang, Xiaolei
Enantioselective α-Functionalization of 1,3-Dithianes by Iridium-Catalyzed Allylic Substitution.
The Journal of organic chemistry, 2020, 85, 12456-12467
4038798 CIFC128.25 H170.25 Cl6.75 O6P -112.959; 15.165; 29.378
75.8; 86.69; 86.896
5583Iuliano, Veronica; Talotta, Carmen; Gaeta, Carmine; Hickey, Neal; Geremia, Silvano; Vatsouro, Ivan; Kovalev, Vladimir; Neri, Placido
Influence of <i>exo</i>-Adamantyl Groups and <i>endo</i>-OH Functions on the Threading of Calix[6]arene Macrocycle.
The Journal of organic chemistry, 2020, 85, 12585-12593
4038799 CIFC112 H136 Cl12 O6P -112.338; 15.813; 15.886
62.331; 80.881; 68.02
2545Iuliano, Veronica; Talotta, Carmen; Gaeta, Carmine; Hickey, Neal; Geremia, Silvano; Vatsouro, Ivan; Kovalev, Vladimir; Neri, Placido
Influence of <i>exo</i>-Adamantyl Groups and <i>endo</i>-OH Functions on the Threading of Calix[6]arene Macrocycle.
The Journal of organic chemistry, 2020, 85, 12585-12593
4038800 CIFC28 H24 N2P 1 21/n 112.124; 21.984; 16.7347
90; 96.781; 90
4429.2Rakshit, Amitava; Kumar, Prashant; Alam, Tipu; Dhara, Hirendranath; Patel, Bhisma K.
Visible-Light-Accelerated Pd-Catalyzed Cascade Addition/Cyclization of Arylboronic Acids to γ- and β-Ketodinitriles for the Construction of 3-Cyanopyridines and 3-Cyanopyrrole Analogues.
The Journal of organic chemistry, 2020, 85, 12482-12504
4038801 CIFC21 H20 Br N O2 SP 1 21/c 113.6616; 9.18547; 17.0339
90; 112.93; 90
1968.65Deng, Qingsong; Yu, Aimin; Zhou, Jie; Cao, Qin; Meng, Xiangtai
Construction of Benzothiophene or Benzothiopheno[2,3-<i>e</i>]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences.
The Journal of organic chemistry, 2020, 85, 12270-12283
4038802 CIFC23 H19 N O3 SC 1 2/c 117.59534; 10.30762; 22.2729
90; 106.229; 90
3878.58Deng, Qingsong; Yu, Aimin; Zhou, Jie; Cao, Qin; Meng, Xiangtai
Construction of Benzothiophene or Benzothiopheno[2,3-<i>e</i>]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences.
The Journal of organic chemistry, 2020, 85, 12270-12283
4038803 CIFC21 H21 N O2 SP n a 2121.6005; 9.3977; 18.9366
90; 90; 90
3844Deng, Qingsong; Yu, Aimin; Zhou, Jie; Cao, Qin; Meng, Xiangtai
Construction of Benzothiophene or Benzothiopheno[2,3-<i>e</i>]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences.
The Journal of organic chemistry, 2020, 85, 12270-12283
4038804 CIFC24 H17 N O3 SP -19.6034; 10.0317; 12.4075
99.201; 111.404; 102.937
1045.48Deng, Qingsong; Yu, Aimin; Zhou, Jie; Cao, Qin; Meng, Xiangtai
Construction of Benzothiophene or Benzothiopheno[2,3-<i>e</i>]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences.
The Journal of organic chemistry, 2020, 85, 12270-12283
4038805 CIFC26 H21 N O2 SP 1 21/c 115.6423; 16.3109; 8.6514
90; 101.62; 90
2162.1Deng, Qingsong; Yu, Aimin; Zhou, Jie; Cao, Qin; Meng, Xiangtai
Construction of Benzothiophene or Benzothiopheno[2,3-<i>e</i>]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences.
The Journal of organic chemistry, 2020, 85, 12270-12283
4038806 CIFC25 H18 F N O2 SP n a 2113.6766; 12.8566; 11.474
90; 90; 90
2017.5Deng, Qingsong; Yu, Aimin; Zhou, Jie; Cao, Qin; Meng, Xiangtai
Construction of Benzothiophene or Benzothiopheno[2,3-<i>e</i>]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences.
The Journal of organic chemistry, 2020, 85, 12270-12283
4038807 CIFC22.5 H22 Cl N O2 SC 1 2/c 127.805; 10.095; 15.272
90; 96.621; 90
4258.1Deng, Qingsong; Yu, Aimin; Zhou, Jie; Cao, Qin; Meng, Xiangtai
Construction of Benzothiophene or Benzothiopheno[2,3-<i>e</i>]azepinedione Derivatives via Three-Component Domino or One-Pot Sequences.
The Journal of organic chemistry, 2020, 85, 12270-12283
4038808 CIFC45 H71 Cl2 O3 P2 RhP -110.92844; 12.69071; 18.62518
105.902; 94.5863; 113.405
2227.08Rodstein, Ilja; Prendes, Daniel Sowa; Wickert, Leon; Paaßen, Maurice; Gessner, Viktoria
Selective Pd-Catalyzed Monoarylation of Small Primary Alkyl Amines through Backbone-Modification in Ylide-Functionalized Phosphines (YPhos).
The Journal of organic chemistry, 2020
4038809 CIFC48 H81.54 Au Cl O2 P2P 1 21/n 113.14401; 24.0935; 14.52671
90; 95.1545; 90
4581.79Rodstein, Ilja; Prendes, Daniel Sowa; Wickert, Leon; Paaßen, Maurice; Gessner, Viktoria
Selective Pd-Catalyzed Monoarylation of Small Primary Alkyl Amines through Backbone-Modification in Ylide-Functionalized Phosphines (YPhos).
The Journal of organic chemistry, 2020
4038810 CIFC80 H132 Au2 Cl2 O P4P -110.22661; 10.50804; 18.1253
86.2203; 86.1003; 79.6142
1908.57Rodstein, Ilja; Prendes, Daniel Sowa; Wickert, Leon; Paaßen, Maurice; Gessner, Viktoria
Selective Pd-Catalyzed Monoarylation of Small Primary Alkyl Amines through Backbone-Modification in Ylide-Functionalized Phosphines (YPhos).
The Journal of organic chemistry, 2020
4038811 CIFC44 H68 P2P -19.3707; 9.9337; 10.031
90.2806; 93.674; 93.3011
930.24Rodstein, Ilja; Prendes, Daniel Sowa; Wickert, Leon; Paaßen, Maurice; Gessner, Viktoria
Selective Pd-Catalyzed Monoarylation of Small Primary Alkyl Amines through Backbone-Modification in Ylide-Functionalized Phosphines (YPhos).
The Journal of organic chemistry, 2020
4038812 CIFC38 H62 P2P 1 21/c 110.29035; 20.32473; 16.76223
90; 100.361; 90
3448.63Rodstein, Ilja; Prendes, Daniel Sowa; Wickert, Leon; Paaßen, Maurice; Gessner, Viktoria
Selective Pd-Catalyzed Monoarylation of Small Primary Alkyl Amines through Backbone-Modification in Ylide-Functionalized Phosphines (YPhos).
The Journal of organic chemistry, 2020
4038813 CIFC40 H66 P2P -110.1846; 10.2395; 18.2242
87.933; 86.219; 69.477
1775.85Rodstein, Ilja; Prendes, Daniel Sowa; Wickert, Leon; Paaßen, Maurice; Gessner, Viktoria
Selective Pd-Catalyzed Monoarylation of Small Primary Alkyl Amines through Backbone-Modification in Ylide-Functionalized Phosphines (YPhos).
The Journal of organic chemistry, 2020
4038814 CIFC14 H15 NP 1 21/c 18.7772; 14.3162; 17.4904
90; 97.518; 90
2178.88Rodstein, Ilja; Prendes, Daniel Sowa; Wickert, Leon; Paaßen, Maurice; Gessner, Viktoria
Selective Pd-Catalyzed Monoarylation of Small Primary Alkyl Amines through Backbone-Modification in Ylide-Functionalized Phosphines (YPhos).
The Journal of organic chemistry, 2020
4038815 CIFC19 H20 B F4 N OP 1 21/n 115.456; 7.0443; 16.266
90; 91.746; 90
1770.2Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038816 CIFC18 H18 B F4 N OP -19.2376; 16.4663; 23.0599
101.102; 91.828; 103.786
3331.7Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038817 CIFC22 H20 B F4 NP 1 21/n 112.0267; 8.0762; 19.1306
90; 96.044; 90
1847.83Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038818 CIFC18 H21 B F4 N2P 1 21/c 112.1916; 9.9536; 14.3268
90; 100.697; 90
1708.35Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038819 CIFC19 H14 B F4 NP 1 21/n 18.3874; 12.2927; 15.2185
90; 99.854; 90
1545.94Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038820 CIFC17 H15 N OP n a 216.165; 17.073; 12.098
90; 90; 90
1273.4Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038821 CIFC18 H15 N OP 1 21/c 19.4054; 14.334; 9.7907
90; 91.688; 90
1319.4Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038822 CIFC26 H20 B2 F8 N2 OP 1 21/c 114.3987; 13.0464; 12.6405
90; 99.152; 90
2344.3Pozharskii, Alexander F.; Dyablo, Olga V.; Pogosova, Olga G.; Ozeryanskii, Valery A.; Filarowski, Aleksander; Vasilikhina, Kseniya M.; Dzhangiryan, Narek A.
Modeling Biologically Important NH···π Interactions Using <i>peri</i>-Disubstituted Naphthalenes.
The Journal of organic chemistry, 2020, 85, 12468-12481
4038823 CIFC18 H14 N2 O3P 21 21 218.0529; 8.1749; 22.1907
90; 90; 90
1460.85Mittendorf, Fabia; Mohr, Fabian; Kirsch, Stefan F.
Ring Expansion of 2-Azido-2-phenyl-indan-1,3-dione for the Generation of Heterocyclic Scaffolds.
The Journal of organic chemistry, 2020, 85, 12760-12769
4038824 CIFC23 H20 N2 O3P 1 21/n 113.0463; 12.6415; 22.773
90; 105.273; 90
3623.2Mittendorf, Fabia; Mohr, Fabian; Kirsch, Stefan F.
Ring Expansion of 2-Azido-2-phenyl-indan-1,3-dione for the Generation of Heterocyclic Scaffolds.
The Journal of organic chemistry, 2020, 85, 12760-12769
4038825 CIFC40 H28 N6 O2P -111.3043; 11.6698; 13.0106
93.163; 100.157; 107.529
1600.24Tasior, Mariusz; Vakuliuk, Olena; Koga, Daiki; Koszarna, Beata; Górski, Krzysztof; Grzybowski, Marek; Kielesiński, Łukasz; Krzeszewski, Maciej; Gryko, Daniel T.
Method for the Large-Scale Synthesis of Multifunctional 1,4-Dihydro-pyrrolo[3,2-<i>b</i>]pyrroles.
The Journal of organic chemistry, 2020
4038826 CIFC42 H30 F12 N2P 1 21/n 16.0701; 25.7968; 10.8547
90; 97.551; 90
1684.99Tasior, Mariusz; Vakuliuk, Olena; Koga, Daiki; Koszarna, Beata; Górski, Krzysztof; Grzybowski, Marek; Kielesiński, Łukasz; Krzeszewski, Maciej; Gryko, Daniel T.
Method for the Large-Scale Synthesis of Multifunctional 1,4-Dihydro-pyrrolo[3,2-<i>b</i>]pyrroles.
The Journal of organic chemistry, 2020
4038827 CIFC22 H27 N3C 1 2/c 122.445; 10.5768; 8.1673
90; 92.685; 90
1936.8Zhang, Zengyu; Huang, Shiqing; Huang, Linwei; Xu, Xingyu; Zhao, Hongyan; Yan, Xiaoyu
Synthesis of Mesoionic N-Heterocyclic Olefins and Catalytic Application for Hydroboration Reactions.
The Journal of organic chemistry, 2020, 85, 12036-12043
4038828 CIFC28 H39 N3P -18.9279; 12.3384; 13.3669
66.588; 81.982; 72.54
1288.6Zhang, Zengyu; Huang, Shiqing; Huang, Linwei; Xu, Xingyu; Zhao, Hongyan; Yan, Xiaoyu
Synthesis of Mesoionic N-Heterocyclic Olefins and Catalytic Application for Hydroboration Reactions.
The Journal of organic chemistry, 2020, 85, 12036-12043
4038829 CIFC20 H27 N O2 P2P 21 21 219.851; 11.5233; 17.2368
90; 90; 90
1956.65Moritz, Jan-Ole; Chakrabortty, Soumyadeep; Müller, Bernd H; Spannenberg, Anke; Kamer, Paul C. J.
P-chirogenic Diphosphazanes with Axially Chiral Substituents and their Use in Rh-catalyzed Asymmetric Hydrogenation.
The Journal of organic chemistry, 2020
4038830 CIFC24 H39 Li N3 PP 1 21 18.8123; 30.9425; 9.2575
90; 98.8763; 90
2494.05Moritz, Jan-Ole; Chakrabortty, Soumyadeep; Müller, Bernd H; Spannenberg, Anke; Kamer, Paul C. J.
P-chirogenic Diphosphazanes with Axially Chiral Substituents and their Use in Rh-catalyzed Asymmetric Hydrogenation.
The Journal of organic chemistry, 2020
4038831 CIFC20 H27 N O2 P2P 21 21 219.856; 11.5291; 17.2583
90; 90; 90
1961.07Moritz, Jan-Ole; Chakrabortty, Soumyadeep; Müller, Bernd H; Spannenberg, Anke; Kamer, Paul C. J.
P-chirogenic Diphosphazanes with Axially Chiral Substituents and their Use in Rh-catalyzed Asymmetric Hydrogenation.
The Journal of organic chemistry, 2020
4038832 CIFC40 H54 B F4 N2 O4 P4 RhP 1 21 110.8041; 15.3336; 13.3346
90; 102.262; 90
2158.7Moritz, Jan-Ole; Chakrabortty, Soumyadeep; Müller, Bernd H; Spannenberg, Anke; Kamer, Paul C. J.
P-chirogenic Diphosphazanes with Axially Chiral Substituents and their Use in Rh-catalyzed Asymmetric Hydrogenation.
The Journal of organic chemistry, 2020
4038833 CIFC23 H16 B F3 N2 OP 1 21/c 19.638; 16.4283; 12.1516
90; 105.707; 90
1852.2Yang, Tianbao; Cao, Xin; Zhang, Xing-Xing; Ou, Yifeng; Au, Chak-Tong; Yin, Shuang-Feng; Qiu, Renhua
Iodine-Catalyzed Synthesis of <i>N,N</i>'-Chelate Organoboron Aminoquinolate.
The Journal of organic chemistry, 2020, 85, 12430-12443
4038834 CIFC25 H17 B Br F3 N2 O4P 1 21/c 117.3714; 14.8912; 9.2154
90; 104.076; 90
2312.27Yang, Tianbao; Cao, Xin; Zhang, Xing-Xing; Ou, Yifeng; Au, Chak-Tong; Yin, Shuang-Feng; Qiu, Renhua
Iodine-Catalyzed Synthesis of <i>N,N</i>'-Chelate Organoboron Aminoquinolate.
The Journal of organic chemistry, 2020, 85, 12430-12443

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