Crystallography Open Database

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7133178 CIFC23 H18 N2 O5P 1 21/c 111.6492; 7.4491; 22.0277
90; 97.248; 90
1896.2He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-Catalyzed Dearomative [3 + 2] Cycloaddition of 4-Nitroisoxazoles with Allenoates or Morita−Baylis−Hillman Carbonates
Chemical Communications, 2024
7133179 CIFC15 H12 N4 O5 SP 1 21/c 113.0981; 11.5834; 10.0872
90; 100.284; 90
1505.85He, Yongjun; He, Tian-Juan; Cheng, Xiufang; Wei, Yibo; Wang, Huamin; Lin, Ying-Wu
Phosphine-Catalyzed Dearomative [3 + 2] Cycloaddition of 4-Nitroisoxazoles with Allenoates or Morita−Baylis−Hillman Carbonates
Chemical Communications, 2024
7133180 CIFC37 H39 B O2 SiC 1 2/c 116.206; 14.988; 26.246
90; 99.955; 90
6279Fujii, Ikuya; Hirata, Haruka; Moniwa, Hirokazu; Shintani, Ryo
Synthesis of (1-silyl)allylboronates by KOtBu-catalyzed ring-opening gem-silylborylation of cyclopropenes
Chemical Communications, 2024
7133181 CIFC29 H46 Cr O2 P2P -110.4305; 10.4775; 14.5388
78.486; 83.946; 71.492
1474.9Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martin A.; Arulsamy, Navamoney; Mock, Michael Thomas
Dinitrogen Activation at Chromium by Photochemically Induced CrII−C Bond Homolysis
Chemical Communications, 2024
7133182 CIFC29 H46 Cr O2 P2P 1 21 18.2502; 15.8605; 11.8231
90; 106.188; 90
1485.74Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martin A.; Arulsamy, Navamoney; Mock, Michael Thomas
Dinitrogen Activation at Chromium by Photochemically Induced CrII−C Bond Homolysis
Chemical Communications, 2024
7133183 CIFC46 H83 Cr2 N2 O4.5 P4P 1 21/n 115.7583; 14.4111; 24.856
90; 107.974; 90
5369.2Duletski, Olivia L.; Platz, Duncan; Pollock, Charlie J.; Mosquera, Martin A.; Arulsamy, Navamoney; Mock, Michael Thomas
Dinitrogen Activation at Chromium by Photochemically Induced CrII−C Bond Homolysis
Chemical Communications, 2024
7133184 CIFC26 H21 N O4P 1 21 16.9055; 21.4299; 27.6189
90; 92.031; 90
4084.6Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4H-benzo[d][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles
Chemical Communications, 2024
7133185 CIFC24 H21 Cl N2 O3P -19.6896; 10.1998; 10.8323
89.99; 71.675; 84.875
1011.78Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4H-benzo[d][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles
Chemical Communications, 2024
7133186 CIFC34 H30 N2 O3P 1 21/c 111.847; 18.1061; 13.0266
90; 95.964; 90
2779.1Wang, Tao; Lu, Zhongyue; Li, Pengfei
Catalyst-free reaction of 2-(4H-benzo[d][1,3]oxazin-4-yl)acrylates: synthesis of 1,2-dihydroquinolines and 2,3-dihydropyrroles
Chemical Communications, 2024
7133187 CIFC10 H11 N O3P 1 21/c 19.9227; 5.672; 16.1656
90; 99.498; 90
897.35Winter, Johannes; Lühr, Susan; Hochadel, Kyra; Gálvez-Vázquez, María de Jesus; Prenzel, Tobias; Schollmeyer, Dieter; Waldvogel, Siegfried R.
Simple Electrochemical Synthesis of Cyclic Hydroxamic Acids by Reduction of Nitro Arenes
Chemical Communications, 2024
7133188 CIFC81 H106 N2 O18P 1 21/c 112.3241; 33.684; 20.229
90; 96.013; 90
8351Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024
7133189 CIFC93 H110 N6 O14P -112.08; 12.4509; 29.1324
94.272; 92.465; 106.74
4174.8Li, Bin; Wang, Yun; Wang, Yuan; Liu, Yue; Wang, Lu; Zhang, Zhi-Yuan; Li, Chunju
Vapochromic separation of toluene and pyridine azeotropes using adaptive macrocycle co-crystals.
Chemical communications (Cambridge, England), 2024
7133190 CIFC52 H76 Fe N2 O2P -19.5346; 13.1604; 18.8315
91.84; 90.463; 91.367
2361Wathsala Kulathungage, Lakshani; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient Carbene Transfer Reactivity Mediated by Fe(II) Complexes Supported by Bulky Alkoxides
Chemical Communications, 2024
7133191 CIFC37 H28 O8P 1 21/c 110.323; 19.0774; 8.7024
90; 114.576; 90
1558.56Wathsala Kulathungage, Lakshani; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient Carbene Transfer Reactivity Mediated by Fe(II) Complexes Supported by Bulky Alkoxides
Chemical Communications, 2024
7133192 CIFC5 H6 O4P -15.006; 7.2628; 8.6451
106.71; 102.405; 92.116
292.37Wathsala Kulathungage, Lakshani; Kurup, Sudheer S.; Browne, Edison A.; Spalink, Gabriel H.; Ward, Cassandra L.; Lord, Richard L.; Groysman, Stanislav
Efficient Carbene Transfer Reactivity Mediated by Fe(II) Complexes Supported by Bulky Alkoxides
Chemical Communications, 2024
7133193 CIFC26.9 H40.71 Cl6.1 Ga2 N4 O P PtP -18.30726; 15.0654; 15.9963
70.9877; 84.8936; 79.8892
1862.28Govindarajan, Ramadoss; Vardhanapu, Pavan Kumar; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from PtII to gallium and indium
Chemical Communications, 2024
7133194 CIFC27 H41 Cl6 In2 N4 O P PtP 1 21/n 18.88651; 12.2296; 35.1991
90; 93.5845; 90
3817.9Govindarajan, Ramadoss; Vardhanapu, Pavan Kumar; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from PtII to gallium and indium
Chemical Communications, 2024
7133195 CIFC28.77 H41.3 Cl6.23 In2 N4 O P PtP -18.71612; 14.4778; 17.6581
65.9038; 81.2608; 73.8299
1951.78Govindarajan, Ramadoss; Vardhanapu, Pavan Kumar; Fayzullin, Robert R.; Khaskin, Eugene; Khusnutdinova, Julia R.
Facile methyl group transfer from PtII to gallium and indium
Chemical Communications, 2024
7133196 CIFC28 H22 N O2 PP -19.2305; 9.3886; 15.0613
83.016; 81.79; 62.191
1140.4Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: Access to 2-phosphinoyl indoles/indol-3-ols
Chemical Communications, 2024
7133197 CIFC29 H24 N O3 PP -110.1021; 10.6285; 12.0861
95.272; 112.661; 92.657
1187.71Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: Access to 2-phosphinoyl indoles/indol-3-ols
Chemical Communications, 2024
7133198 CIFC29.6 H25.2 Cl1.2 N O3 PP -19.9338; 11.4115; 13.4261
91.104; 99.247; 107.898
1425.68Liu, Yong; Jia, Mengying; Wang, Guodong; Yang, Wenhui; Xu, Xianxiu
Silver-catalyzed P-centered anion nucleophilic addition to isocyanide: Access to 2-phosphinoyl indoles/indol-3-ols
Chemical Communications, 2024
7133199 CIFC46 H41 N2 O8 S2P -110.581; 10.781; 20.524
88.303; 85.635; 63.604
2091.1Bhati, Kuldeep Singh; Sharma, Siddharth
Electrochemically-Driven Difunctionalization of Isocyanide and Mumm Rearrangement Cascade: Expeditious Synthesis of N-acyl-N-alkyl S-thiocarbamates.
Chemical Communications, 2024
7133200 CIFC26 H19 Cl F6 N2 O4P b c n16.652; 14.997; 21.13
90; 90; 90
5276.8Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
N-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction via α–C(sp3)−H activation strategy
Chemical Communications, 2024
7133201 CIFC15 H13 N O2C 1 2/c 112.719; 13.852; 14.156
90; 97.096; 90
2475Tang, Yong-Xing; Zhou, You; Wu, Hao-Xuan; Wang, Li-Sheng; Wu, Chun-Yan; Zhuang, Shi-Yi; Wu, An-Xin
N-Benzylhydroxylamine as a novel synthetic block in "C1N1" embedding reaction via α–C(sp3)−H activation strategy
Chemical Communications, 2024
7133202 CIFC38 H28 O3 P2P b c a16.51047; 16.41081; 23.08005
90; 90; 90
6253.54Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133203 CIFC19 H13 P SC 1 2/c 114.248; 13.5359; 15.8127
90; 90.772; 90
3049.35Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133204 CIFC24 H22 N O PP n a 2117.3159; 9.40206; 12.4887
90; 90; 90
2033.22Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133205 CIFC19 H13 P SeC 1 2/c 114.1963; 13.7375; 15.8281
90; 90.897; 90
3086.4Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133206 CIFC26 H20 N O2 P SP 1 21/c 18.19512; 13.942; 19.4641
90; 99.7093; 90
2192.04Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133207 CIFC34 H36 N O2 P SP 21 21 219.31097; 12.97197; 24.0692
90; 90; 90
2907.12Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133208 CIFC44 H33 B F4 N PP c a 2112.867; 13.069; 21.505
90; 90; 90
3616.3Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133209 CIFC25.5 H19 B Cl F3 N PP 1 21/c 19.5904; 16.0488; 14.2154
90; 101.406; 90
2144.74Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133210 CIFC31 H23 N O3 P2P 1 21/c 111.81181; 19.91502; 11.98573
90; 118.939; 90
2467.38Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133211 CIFC38 H28 O3 P2P b c a16.3712; 16.281; 22.9501
90; 90; 90
6117.11Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133212 CIFC19 H14 O2 PC 1 2/c 120.3958; 13.4454; 12.1945
90; 117.604; 90
2963.44Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133213 CIFC19 H13 P SeC 1 2/c 114.0369; 13.6803; 15.7202
90; 90.789; 90
3018.45Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133214 CIFC19 H13 O PP -17.2774; 8.0944; 13.1388
81.7506; 79.8049; 70.6319
715.63Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133215 CIFC25 H18 N PP 21 21 218.9413; 13.6176; 15.5673
90; 90; 90
1895.46Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133216 CIFC44 H20 B Cl2 F15 N PP -111.2365; 12.2624; 14.8185
83.39; 78.06; 74.601
1921.98Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133217 CIFC31 H30 N PP 1 21/n 19.0484; 18.306; 14.4219
90; 90.4144; 90
2388.78Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133218 CIFC27 H19 F6 N2 O4 P S2P -18.3718; 17.3368; 20.1621
113.925; 91.4063; 93.9353
2664.18Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133219 CIFC19 H13 P SC 1 2/c 114.0811; 13.4388; 15.6879
90; 90.464; 90
2968.57Hu, Lei; Chakraborty, Sayandip; Tumanov, Nikolay; Wouters, Johan; Robiette, Raphaël; Berionni, Guillaume
Regulating iminophosphorane PN bond reactivity through geometric constraints with cage-shaped triarylphosphines.
Chemical communications (Cambridge, England), 2024
7133220 CIFC27 H38 N2 O5 S SiP 1 21 18.956; 12.4093; 12.9018
90; 95.349; 90
1427.63Mroczyńska, Karina; Dobrzańska, Liliana; Rafiński, Zbigniew
Enantioselective Synthesis of C3-Functionalized 2,1-Benzothiazine 2,2-Dioxides by N-Heterocyclic Carbene Catalysis
Chemical Communications, 2024
7133221 CIFC41 H35 Cl3 N0.5 O5 PP -111.7184; 12.545; 14.696
101.781; 98.985; 114.481
1853.15Zhou, Xiaocong; Wang, Jian; Shen, Yirui; Ma, Dumei; Zhao, Yufen; Wu, Ju
Electrochemical Synthesis of Phosphorylated Azaspiro[4.5]di/trienones through Dearomative Spirocyclization
Chemical Communications, 2024
7133222 CIFC58 H51.67 N2 O8 P2P b c a21.3419; 21.1766; 21.9827
90; 90; 90
9935.1Zhou, Xiaocong; Wang, Jian; Shen, Yirui; Ma, Dumei; Zhao, Yufen; Wu, Ju
Electrochemical Synthesis of Phosphorylated Azaspiro[4.5]di/trienones through Dearomative Spirocyclization
Chemical Communications, 2024
7133223 CIFC29 H24 Cl4 F N O2 PP -110.835; 12.7978; 20.779
81.75; 80.192; 89.486
2809.45Zhou, Xiaocong; Wang, Jian; Shen, Yirui; Ma, Dumei; Zhao, Yufen; Wu, Ju
Electrochemical Synthesis of Phosphorylated Azaspiro[4.5]di/trienones through Dearomative Spirocyclization
Chemical Communications, 2024

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