Crystallography Open Database

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7121124 CIFC58 H44 Br2 P2 PdP 1 21/c 111.581; 18.509; 22.7
90; 100.345; 90		4786.7Wang, Yanqing; Nakajima, Kiyohiko; Song, Zhiyi; Takahashi, Tamotsu
Lithiation of palladated dihydropentacene: a new route for the introduction of substituents from both of electrophiles and nucleophiles to pentacene.
Chemical communications (Cambridge, England), 2018, 54, 1265-1268
7121125 CIFC K3 O8 VC 1 m 19; 9.297; 5.601
90; 122.89; 90		394Song, Yunxia; Luo, Min; Liang, Fei; Ye, Ning; Lin, Zheshuai
The second-harmonic generation intensification derived from localization conjugated π-orbitals in O<sub>2</sub><sup>2</sup>.
Chemical communications (Cambridge, England), 2018, 54, 1445-1448
7121126 CIFC24 Fe8 Ge12 I4 O24P 1 21/n 111.8483; 18.548; 12.1901
90; 110.483; 90		2509.55Wolf, Silke; Klopper, Wim; Feldmann, Claus
Ge<sub>12</sub>{Fe(CO)<sub>3</sub>}<sub>8</sub>(μ-I)<sub>4</sub>: a germanium-iron cluster with Ge<sub>4</sub>, Ge<sub>2</sub> and Ge units.
Chemical communications (Cambridge, England), 2018, 54, 1217-1220
7121127 CIFC10 H6 Cl3 N O2P 1 21/c 121.1155; 4.9816; 21.6442
90; 111.532; 90		2117.84Kubanik, Mario; Lam, Nelson Y. S.; Holtkamp, Hannah U.; Söhnel, Tilo; Anderson, Robert F.; Jamieson, Stephen M. F.; Hartinger, Christian G.
Quinoline-para-quinones and metals: coordination-assisted formation of quinoline-ortho-quinones.
Chemical communications (Cambridge, England), 2018, 54, 992-995
7121128 CIFC20 H18 Cl5 N O3 OsP 1 21/c 110.3571; 21.0903; 10.705
90; 108.136; 90		2222.2Kubanik, Mario; Lam, Nelson Y. S.; Holtkamp, Hannah U.; Söhnel, Tilo; Anderson, Robert F.; Jamieson, Stephen M. F.; Hartinger, Christian G.
Quinoline-para-quinones and metals: coordination-assisted formation of quinoline-ortho-quinones.
Chemical communications (Cambridge, England), 2018, 54, 992-995
7121129 CIFC19 H18 Cl2 Ir N O3P 1 21/c 114.4492; 7.3746; 17.1873
90; 92.4; 90		1829.82Kubanik, Mario; Lam, Nelson Y. S.; Holtkamp, Hannah U.; Söhnel, Tilo; Anderson, Robert F.; Jamieson, Stephen M. F.; Hartinger, Christian G.
Quinoline-para-quinones and metals: coordination-assisted formation of quinoline-ortho-quinones.
Chemical communications (Cambridge, England), 2018, 54, 992-995
7121130 CIFC19 H18 Cl2 N O3 RhP 1 21/c 114.473; 7.3041; 17.2691
90; 92.709; 90		1823.52Kubanik, Mario; Lam, Nelson Y. S.; Holtkamp, Hannah U.; Söhnel, Tilo; Anderson, Robert F.; Jamieson, Stephen M. F.; Hartinger, Christian G.
Quinoline-para-quinones and metals: coordination-assisted formation of quinoline-ortho-quinones.
Chemical communications (Cambridge, England), 2018, 54, 992-995
7121131 CIFC20 H19 Cl4 N O3 RuP 1 21/c 110.6343; 21.127; 19.5934
90; 100.782; 90		4324.4Kubanik, Mario; Lam, Nelson Y. S.; Holtkamp, Hannah U.; Söhnel, Tilo; Anderson, Robert F.; Jamieson, Stephen M. F.; Hartinger, Christian G.
Quinoline-para-quinones and metals: coordination-assisted formation of quinoline-ortho-quinones.
Chemical communications (Cambridge, England), 2018, 54, 992-995
7121132 CIFC15 H12 N O S2P 1 21/c 110.834; 10.782; 11.696
90; 93.39; 90		1363.8Mahato, Karuna; Arora, Neha; Ray Bagdi, Prasanta; Gattu, Radhakrishna; Ghosh, Siddhartha Sankar; Khan, Abu T.
An oxidative cross-coupling reaction of 4-hydroxydithiocoumarin and amines/thiols using a combination of I<sub>2</sub> and TBHP: access to lead molecules for biomedical applications.
Chemical communications (Cambridge, England), 2018, 54, 1513-1516
7121133 CIFC16 H13 N O3 S2P 1 21 110.3912; 5.6999; 12.8081
90; 102.459; 90		740.74Mahato, Karuna; Arora, Neha; Ray Bagdi, Prasanta; Gattu, Radhakrishna; Ghosh, Siddhartha Sankar; Khan, Abu T.
An oxidative cross-coupling reaction of 4-hydroxydithiocoumarin and amines/thiols using a combination of I<sub>2</sub> and TBHP: access to lead molecules for biomedical applications.
Chemical communications (Cambridge, England), 2018, 54, 1513-1516
7121134 CIFC23 H17 N O2 S2P 1 21/c 116.5683; 13.2261; 8.5713
90; 95.047; 90		1870.98Mahato, Karuna; Arora, Neha; Ray Bagdi, Prasanta; Gattu, Radhakrishna; Ghosh, Siddhartha Sankar; Khan, Abu T.
An oxidative cross-coupling reaction of 4-hydroxydithiocoumarin and amines/thiols using a combination of I<sub>2</sub> and TBHP: access to lead molecules for biomedical applications.
Chemical communications (Cambridge, England), 2018, 54, 1513-1516
7121135 CIFC48 H30 N18 O13 Zn4P -124.187; 24.1807; 24.292
59.829; 89.966; 60.346		10075Ishiwata, Takumi; Michibata, Ayano; Kokado, Kenta; Ferlay, Sylvie; Hosseini, Mir Wais; Sada, Kazuki
Box-like gel capsules from heterostructures based on a core-shell MOF as a template of crystal crosslinking.
Chemical communications (Cambridge, England), 2018, 54, 1437-1440
7121136 CIFC63 H92 N8 O8 P4 S4P -114.6456; 15.5637; 17.4714
67.92; 78.389; 73.028		3510.8Koner, Abhishek; Kelemen, Zsolt; Schnakenburg, Gregor; Nyulászi, László; Streubel, Rainer
1,4-Additions of tricyclic 1,4-diphosphinines - a novel system to study σ-bond activation and π-π dispersion interactions.
Chemical communications (Cambridge, England), 2018, 54, 1182-1184
7121137 CIFC34 H46 N4 P2 S4P 1 21/c 118.465; 13.1095; 15.633
90; 103.23; 90		3683.8Koner, Abhishek; Kelemen, Zsolt; Schnakenburg, Gregor; Nyulászi, László; Streubel, Rainer
1,4-Additions of tricyclic 1,4-diphosphinines - a novel system to study σ-bond activation and π-π dispersion interactions.
Chemical communications (Cambridge, England), 2018, 54, 1182-1184
7121138 CIFC129 H174 Cl2 N20 O8 P8 S8C 1 2/c 127.7111; 14.5378; 21.9682
90; 126.366; 90		7126.5Koner, Abhishek; Kelemen, Zsolt; Schnakenburg, Gregor; Nyulászi, László; Streubel, Rainer
1,4-Additions of tricyclic 1,4-diphosphinines - a novel system to study σ-bond activation and π-π dispersion interactions.
Chemical communications (Cambridge, England), 2018, 54, 1182-1184
7121139 CIFC34 H46 N4 P2 S2 Se2P 1 21/c 118.5972; 13.2665; 15.6185
90; 103.28; 90		3750.4Koner, Abhishek; Kelemen, Zsolt; Schnakenburg, Gregor; Nyulászi, László; Streubel, Rainer
1,4-Additions of tricyclic 1,4-diphosphinines - a novel system to study σ-bond activation and π-π dispersion interactions.
Chemical communications (Cambridge, England), 2018, 54, 1182-1184
7121140 CIFC4 H4 Br2 Cu N4 O2 PtP 1 21/m 16.3039; 14.2946; 6.564
90; 110.207; 90		555.09Sergeenko, Ania S.; Ovens, Jeffrey S.; Leznoff, Daniel B.
Designing anisotropic cyanometallate coordination polymers with unidirectional thermal expansion (TE): 2D zero and 1D colossal positive TE.
Chemical communications (Cambridge, England), 2018, 54, 1599-1602
7121142 CIFC99 H155 Ge4P -110.3376; 17.8421; 25.5819
84.4742; 83.1749; 87.3583		4660.37Suzuki, Katsunori; Numata, Yasuyuki; Fujita, Naoko; Hayakawa, Naoki; Tanikawa, Tomoharu; Hashizume, Daisuke; Tamao, Kohei; Fueno, Hiroyuki; Tanaka, Kazuyoshi; Matsuo, Tsukasa
A stable free tetragermacyclobutadiene incorporating fused-ring bulky EMind groups.
Chemical communications (Cambridge, England), 2018, 54, 2200-2203
7121143 CIFC48 H74 Cl2 Ge2P -110.9924; 11.3428; 11.8084
118.544; 92.15; 113.282		1140.33Suzuki, Katsunori; Numata, Yasuyuki; Fujita, Naoko; Hayakawa, Naoki; Tanikawa, Tomoharu; Hashizume, Daisuke; Tamao, Kohei; Fueno, Hiroyuki; Tanaka, Kazuyoshi; Matsuo, Tsukasa
A stable free tetragermacyclobutadiene incorporating fused-ring bulky EMind groups.
Chemical communications (Cambridge, England), 2018, 54, 2200-2203
7121144 CIFC44 H27 F N4 O2C 1 c 124.0426; 14.5938; 20.3274
90; 112.283; 90		6599.7Yu, Ling; Wu, Zhongbin; Xie, Guohua; Zhong, Cheng; Zhu, Zece; Ma, Dongge; Yang, Chuluo
An efficient exciton harvest route for high-performance OLEDs based on aggregation-induced delayed fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 1379-1382
7121145 CIFC44 H26 F2 N4 O2P -111.2482; 11.3076; 13.5181
91.797; 102.745; 101.04		1641.1Yu, Ling; Wu, Zhongbin; Xie, Guohua; Zhong, Cheng; Zhu, Zece; Ma, Dongge; Yang, Chuluo
An efficient exciton harvest route for high-performance OLEDs based on aggregation-induced delayed fluorescence.
Chemical communications (Cambridge, England), 2018, 54, 1379-1382
7121154 CIFC27 H27 F3 N4 O3P 1 21/n 17.3234; 33.2434; 10.4467
90; 104.815; 90		2458.75Lau, Nathanael; Zakharov, Lev N.; Pluth, Michael D.
Modular tripodal receptors for the hydrosulfide (HS<sup>-</sup>) anion.
Chemical communications (Cambridge, England), 2018, 54, 2337-2340
7121155 CIFC30 H27 F9 N4 O3P -18.6772; 12.4885; 14.3777
88.841; 85.99; 69.956		1460.08Lau, Nathanael; Zakharov, Lev N.; Pluth, Michael D.
Modular tripodal receptors for the hydrosulfide (HS<sup>-</sup>) anion.
Chemical communications (Cambridge, England), 2018, 54, 2337-2340
7121156 CIFC30 H27 F9 N4 O3P 1 21/n 115.8131; 8.3293; 24.4837
90; 99.684; 90		3178.85Lau, Nathanael; Zakharov, Lev N.; Pluth, Michael D.
Modular tripodal receptors for the hydrosulfide (HS<sup>-</sup>) anion.
Chemical communications (Cambridge, England), 2018, 54, 2337-2340
7121157 CIFC8 H21 N SR -3 c :H12.0967; 12.0967; 34.713
90; 90; 120		4399Lau, Nathanael; Zakharov, Lev N.; Pluth, Michael D.
Modular tripodal receptors for the hydrosulfide (HS<sup>-</sup>) anion.
Chemical communications (Cambridge, England), 2018, 54, 2337-2340
7121158 CIFC26 H27 N3 O4 SP 21 21 218.6582; 10.5543; 25.8744
90; 90; 90		2364.4Sheng, Guorong; Ma, Shicong; Bai, Songlin; Mao, Jianming; Lu, Ping; Wang, Yanguang
A copper-catalyzed reaction of 3-diazoindolin-2-imines with 2-(phenylamino)ethanols: convenient access to spiro[indoline-3,2'-oxazolidin]-2-imines.
Chemical communications (Cambridge, England), 2018, 54, 1529-1532
7121159 CIFC26 H27 N3 O4 SP 21 21 218.6243; 10.5297; 25.811
90; 90; 90		2343.9Sheng, Guorong; Ma, Shicong; Bai, Songlin; Mao, Jianming; Lu, Ping; Wang, Yanguang
A copper-catalyzed reaction of 3-diazoindolin-2-imines with 2-(phenylamino)ethanols: convenient access to spiro[indoline-3,2'-oxazolidin]-2-imines.
Chemical communications (Cambridge, England), 2018, 54, 1529-1532
7121160 CIFC27 H29 N3 O3 SP -111.0863; 11.6603; 11.8746
109.645; 100.679; 113.71		1228.8Sheng, Guorong; Ma, Shicong; Bai, Songlin; Mao, Jianming; Lu, Ping; Wang, Yanguang
A copper-catalyzed reaction of 3-diazoindolin-2-imines with 2-(phenylamino)ethanols: convenient access to spiro[indoline-3,2'-oxazolidin]-2-imines.
Chemical communications (Cambridge, England), 2018, 54, 1529-1532
7121161 CIFC26 H29 N3 O3 SP 1 21/c 112.1615; 11.8908; 16.8761
90; 98.719; 90		2412.2Sheng, Guorong; Ma, Shicong; Bai, Songlin; Mao, Jianming; Lu, Ping; Wang, Yanguang
A copper-catalyzed reaction of 3-diazoindolin-2-imines with 2-(phenylamino)ethanols: convenient access to spiro[indoline-3,2'-oxazolidin]-2-imines.
Chemical communications (Cambridge, England), 2018, 54, 1529-1532
7121162 CIFC19 H20 N2 O2P 21 21 219.5082; 9.5276; 18.393
90; 90; 90		1666.2Sheng, Guorong; Ma, Shicong; Bai, Songlin; Mao, Jianming; Lu, Ping; Wang, Yanguang
A copper-catalyzed reaction of 3-diazoindolin-2-imines with 2-(phenylamino)ethanols: convenient access to spiro[indoline-3,2'-oxazolidin]-2-imines.
Chemical communications (Cambridge, England), 2018, 54, 1529-1532
7121163 CIFC16 H18 Br3 Co N4P -18.2736; 10.7007; 11.1674
85.313; 71.078; 86.856		931.71Nie, Weixuan; McCrory, Charles C. L.
Electrocatalytic CO<sub>2</sub> reduction by a cobalt bis(pyridylmonoimine) complex: effect of acid concentration on catalyst activity and stability.
Chemical communications (Cambridge, England), 2018, 54, 1579-1582
7121164 CIFC27 H37 B Fe P2P 1 21/c 19.9177; 11.565; 22.0296
90; 93.929; 90		2520.82Lik, Artur; Kargin, Denis; Isenberg, Stefan; Kelemen, Zsolt; Pietschnig, Rudolf; Helten, Holger
PBP bridged [3]ferrocenophane: a bisphosphanylborane with a redox trigger.
Chemical communications (Cambridge, England), 2018, 54, 2471-2474
7121165 CIFC4 H12 Ag10 N16 O44 Si W12I -4 m 214.198; 14.198; 12.297
90; 90; 90		2478.9Li, Shaobin; Zhang, Li; Lan, Yaqian; O'Halloran, Kevin P; Ma, Huiyuan; Pang, Haijun
Polyoxometalate-encapsulated twenty-nuclear silver-tetrazole nanocage frameworks as highly active electrocatalysts for the hydrogen evolution reaction.
Chemical communications (Cambridge, England), 2018, 54, 1964-1967
7121166 CIFC4 H12 Ag10 N16 O44 P W12I -4 m 214.182; 14.182; 12.331
90; 90; 90		2480.1Li, Shaobin; Zhang, Li; Lan, Yaqian; O'Halloran, Kevin P; Ma, Huiyuan; Pang, Haijun
Polyoxometalate-encapsulated twenty-nuclear silver-tetrazole nanocage frameworks as highly active electrocatalysts for the hydrogen evolution reaction.
Chemical communications (Cambridge, England), 2018, 54, 1964-1967
7121169 CIFC32 H36 N4 O5 SP 1 21/c 119.7577; 9.1446; 16.6909
90; 103.132; 90		2936.79Bao, Xiaoping; Wu, Xin; Berry, Stuart N.; Howe, Ethan N. W.; Chang, Young-Tae; Gale, Philip A.
Fluorescent squaramides as anion receptors and transmembrane anion transporters.
Chemical communications (Cambridge, England), 2018, 54, 1363-1366
7121170 CIFC33 H35 N SiP -19.0089; 13.9567; 22.3783
98.702; 99.193; 99.7		2691.6Jiang, Guangbin; Hu, Weigao; Li, Jianxiao; Zhu, Chuanle; Wu, Wanqing; Jiang, Huanfeng
Palladium-catalyzed primary amine-directed regioselective mono- and di-alkynylation of biaryl-2-amines.
Chemical communications (Cambridge, England), 2018, 54, 1746-1749
7121171 CIFC40 H55 N Si2P 1 21/c 115.373; 7.7388; 32.2857
90; 101.174; 90		3768.2Jiang, Guangbin; Hu, Weigao; Li, Jianxiao; Zhu, Chuanle; Wu, Wanqing; Jiang, Huanfeng
Palladium-catalyzed primary amine-directed regioselective mono- and di-alkynylation of biaryl-2-amines.
Chemical communications (Cambridge, England), 2018, 54, 1746-1749
7121172 CIFC30 H32 B Mo N7 O2P -18.0189; 10.2181; 18.5046
77.57; 87.661; 80.033		1458.33Frogley, Benjamin J.; Hill, Anthony F.
A complete set of pnictocarbynes: [M([triple bond, length as m-dash]CAPh<sub>2</sub>)(CO)<sub>2</sub>(Tp*)] (M = Mo, W; A = N, P, As, Sb, Bi; Tp* = hydrotris(dimethylpyrazolyl)-borate).
Chemical communications (Cambridge, England), 2018, 54, 2126-2129
7121173 CIFC30 H32 B Bi N6 O2 WP 1 21 110.216; 14.1835; 10.6359
90; 90.067; 90		1541.13Frogley, Benjamin J.; Hill, Anthony F.
A complete set of pnictocarbynes: [M([triple bond, length as m-dash]CAPh<sub>2</sub>)(CO)<sub>2</sub>(Tp*)] (M = Mo, W; A = N, P, As, Sb, Bi; Tp* = hydrotris(dimethylpyrazolyl)-borate).
Chemical communications (Cambridge, England), 2018, 54, 2126-2129
7121174 CIFC30 H32 B N7 O2 WP -17.9985; 10.1857; 18.51
77.58; 87.554; 79.822		1449.53Frogley, Benjamin J.; Hill, Anthony F.
A complete set of pnictocarbynes: [M([triple bond, length as m-dash]CAPh<sub>2</sub>)(CO)<sub>2</sub>(Tp*)] (M = Mo, W; A = N, P, As, Sb, Bi; Tp* = hydrotris(dimethylpyrazolyl)-borate).
Chemical communications (Cambridge, England), 2018, 54, 2126-2129
7121175 CIFC30 H32 B Bi Mo N6 O2P 1 21 110.231; 14.2033; 10.5668
90; 90.271; 90		1535.49Frogley, Benjamin J.; Hill, Anthony F.
A complete set of pnictocarbynes: [M([triple bond, length as m-dash]CAPh<sub>2</sub>)(CO)<sub>2</sub>(Tp*)] (M = Mo, W; A = N, P, As, Sb, Bi; Tp* = hydrotris(dimethylpyrazolyl)-borate).
Chemical communications (Cambridge, England), 2018, 54, 2126-2129
7121176 CIFC30 H32 As B Mo N6 O2P 1 21/c 110.1096; 31.7822; 19.6195
90; 98.64; 90		6232.31Frogley, Benjamin J.; Hill, Anthony F.
A complete set of pnictocarbynes: [M([triple bond, length as m-dash]CAPh<sub>2</sub>)(CO)<sub>2</sub>(Tp*)] (M = Mo, W; A = N, P, As, Sb, Bi; Tp* = hydrotris(dimethylpyrazolyl)-borate).
Chemical communications (Cambridge, England), 2018, 54, 2126-2129
7121177 CIFC30 H32 As B N6 O2 WP 1 21/c 110.0885; 31.7494; 19.6156
90; 99.29; 90		6200.54Frogley, Benjamin J.; Hill, Anthony F.
A complete set of pnictocarbynes: [M([triple bond, length as m-dash]CAPh<sub>2</sub>)(CO)<sub>2</sub>(Tp*)] (M = Mo, W; A = N, P, As, Sb, Bi; Tp* = hydrotris(dimethylpyrazolyl)-borate).
Chemical communications (Cambridge, England), 2018, 54, 2126-2129
7121178 CIFC25 H25 In N2P 1 21/c 112.3494; 12.6121; 13.8333
90; 98.628; 90		2130.2Gil-Negrete, José M; Pérez Sestelo, José; Sarandeses, Luis A.
Synthesis of bench-stable solid triorganoindium reagents and reactivity in palladium-catalyzed cross-coupling reactions.
Chemical communications (Cambridge, England), 2018, 54, 1453-1456
7121179 CIFC24 H23 N O4P 1 21 19.593; 8; 13.517
90; 103.143; 90		1010.2Cheng, Jian; Xie, Jin; Zhu, Chengjian
Relay photocatalytic cascade reactions: synthesis of indolo[2,1-a]isoquinoline derivatives via double C(sp<sup>3</sup>)-H bond functionalization.
Chemical communications (Cambridge, England), 2018, 54, 1655-1658
7121180 CIFC33 H34 Cl2 N6 O7P -111.1425; 11.9013; 13.4239
100.486; 92.781; 103.209		1696.54He, Haihong; Ye, Zhiwei; Zheng, Ying; Xu, Xiu; Guo, Chunlei; Xiao, Yi; Yang, Wei; Qian, Xuhong; Yang, Youjun
Super-resolution imaging of lysosomes with a nitroso-caged rhodamine.
Chemical communications (Cambridge, England), 2018, 54, 2842-2845
7121181 CIFC14 H10 Br N SP -16.634; 9.3287; 9.7895
82.039; 85.191; 89.175		597.89Huang, Yubing; Yan, Donghao; Wang, Xu; Zhou, Peiqi; Wu, Wanqing; Jiang, Huanfeng
Controllable assembly of the benzothiazole framework using a C[triple bond, length as m-dash]C triple bond as a one-carbon synthon.
Chemical communications (Cambridge, England), 2018, 54, 1742-1745
7121182 CIFC24 H30 N3 O PP 3212.209; 12.209; 12.997
90; 90; 120		1677.8Rajasekar, Prabhakaran; Pandey, Swechchha; Paithankar, Harshad; Chugh, Jeetender; Steiner, Alexander; Boomishankar, Ramamoorthy
Imido-P(v) trianion supported enantiopure neutral tetrahedral Pd(ii) cages.
Chemical communications (Cambridge, England), 2018, 54, 1873-1876
7121183 CIFC108 H108 N12 O28 P4 Pd12F 2 328.288; 28.288; 28.288
90; 90; 90		22636.4Rajasekar, Prabhakaran; Pandey, Swechchha; Paithankar, Harshad; Chugh, Jeetender; Steiner, Alexander; Boomishankar, Ramamoorthy
Imido-P(v) trianion supported enantiopure neutral tetrahedral Pd(ii) cages.
Chemical communications (Cambridge, England), 2018, 54, 1873-1876
7121184 CIFC108 H108 N12 O28 P4 Pd12F 2 328.046; 28.046; 28.046
90; 90; 90		22060.4Rajasekar, Prabhakaran; Pandey, Swechchha; Paithankar, Harshad; Chugh, Jeetender; Steiner, Alexander; Boomishankar, Ramamoorthy
Imido-P(v) trianion supported enantiopure neutral tetrahedral Pd(ii) cages.
Chemical communications (Cambridge, England), 2018, 54, 1873-1876
7121185 CIFC292 H330 N24 O95 P8 Pd24C 1 c 120.679; 25.531; 31.458
90; 94.48; 90		16558Rajasekar, Prabhakaran; Pandey, Swechchha; Paithankar, Harshad; Chugh, Jeetender; Steiner, Alexander; Boomishankar, Ramamoorthy
Imido-P(v) trianion supported enantiopure neutral tetrahedral Pd(ii) cages.
Chemical communications (Cambridge, England), 2018, 54, 1873-1876
7121186 CIFC10 H10 N2P -18.9125; 11.3351; 13.323
69.182; 74.864; 87.348		1212.8Ning, Yingtang; Kawahata, Masatoshi; Yamaguchi, Kentaro; Otani, Yuko; Ohwada, Tomohiko
Synthesis, structure and N-N bonding character of 1,1-disubstituted indazolium hexafluorophosphate.
Chemical communications (Cambridge, England), 2018, 54, 1881-1884
7121187 CIFC14 H17 F6 N2 O PP 1 21/n 19.3512; 14.2117; 12.5086
90; 110.717; 90		1554.9Ning, Yingtang; Kawahata, Masatoshi; Yamaguchi, Kentaro; Otani, Yuko; Ohwada, Tomohiko
Synthesis, structure and N-N bonding character of 1,1-disubstituted indazolium hexafluorophosphate.
Chemical communications (Cambridge, England), 2018, 54, 1881-1884
7121188 CIFC12 H16 Br F6 N2 PP 1 21/n 18.431; 10.6455; 17.7568
90; 91.537; 90		1593.1Ning, Yingtang; Kawahata, Masatoshi; Yamaguchi, Kentaro; Otani, Yuko; Ohwada, Tomohiko
Synthesis, structure and N-N bonding character of 1,1-disubstituted indazolium hexafluorophosphate.
Chemical communications (Cambridge, England), 2018, 54, 1881-1884
7121189 CIFC13 H17 F6 N2 PP 1 21/n 18.8739; 12.9265; 13.4682
90; 99.885; 90		1521.98Ning, Yingtang; Kawahata, Masatoshi; Yamaguchi, Kentaro; Otani, Yuko; Ohwada, Tomohiko
Synthesis, structure and N-N bonding character of 1,1-disubstituted indazolium hexafluorophosphate.
Chemical communications (Cambridge, England), 2018, 54, 1881-1884
7121190 CIFC24 H20 O5P b c a9.52631; 14.5795; 26.9344
90; 90; 90		3740.89Luo, Kui; Zhang, Ling; Jiang, Huanfeng; Chen, Lianfen; Zhu, Shifa
Selectivity-switchable construction of benzo-fused polycyclic compounds through a gold-catalyzed reaction of enyne-lactone.
Chemical communications (Cambridge, England), 2018, 54, 1893-1896
7121191 CIFC21 H15 Br O5P -18.0941; 9.6765; 11.9451
70.653; 81.146; 88.316		871.99Luo, Kui; Zhang, Ling; Jiang, Huanfeng; Chen, Lianfen; Zhu, Shifa
Selectivity-switchable construction of benzo-fused polycyclic compounds through a gold-catalyzed reaction of enyne-lactone.
Chemical communications (Cambridge, England), 2018, 54, 1893-1896
7121192 CIFC21 H16 O5P 1 21/n 112.2774; 10.4052; 13.0395
90; 101.928; 90		1629.81Luo, Kui; Zhang, Ling; Jiang, Huanfeng; Chen, Lianfen; Zhu, Shifa
Selectivity-switchable construction of benzo-fused polycyclic compounds through a gold-catalyzed reaction of enyne-lactone.
Chemical communications (Cambridge, England), 2018, 54, 1893-1896
7121193 CIFC56 H90 Cl2 N2 P2 ZrP 21 21 2113.3448; 25.7942; 31.7835
90; 90; 90		10940.5Grant, Lauren N.; Miehlich, Matthias E.; Meyer, Karsten; Mindiola, Daniel J.
Arrested disproportionation in trivalent, mononuclear, and non-metallocene complexes of Zr(iii) and Hf(iii).
Chemical communications (Cambridge, England), 2018, 54, 2052-2055
7121194 CIFC44 H62 Cl N2 P2 ZrP 1 21/n 117.7014; 13.7831; 17.8222
90; 99.961; 90		4282.7Grant, Lauren N.; Miehlich, Matthias E.; Meyer, Karsten; Mindiola, Daniel J.
Arrested disproportionation in trivalent, mononuclear, and non-metallocene complexes of Zr(iii) and Hf(iii).
Chemical communications (Cambridge, England), 2018, 54, 2052-2055
7121195 CIFC44 H62 Cl Hf N2 P2P 1 21/n 117.727; 13.7111; 17.849
90; 99.773; 90		4275.4Grant, Lauren N.; Miehlich, Matthias E.; Meyer, Karsten; Mindiola, Daniel J.
Arrested disproportionation in trivalent, mononuclear, and non-metallocene complexes of Zr(iii) and Hf(iii).
Chemical communications (Cambridge, England), 2018, 54, 2052-2055
7121196 CIFC58 H78 Cl2 Hf N2 P2P 21 21 2113.3358; 25.5782; 31.842
90; 90; 90		10861.5Grant, Lauren N.; Miehlich, Matthias E.; Meyer, Karsten; Mindiola, Daniel J.
Arrested disproportionation in trivalent, mononuclear, and non-metallocene complexes of Zr(iii) and Hf(iii).
Chemical communications (Cambridge, England), 2018, 54, 2052-2055
7121197 CIFC19 H14 F3 N O2C 1 2/c 119.9333; 9.8491; 16.6571
90; 98.999; 90		3229.95Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Afonin, A. V.; Vashchenko, A. V.; Muzalevskiy, V. M.; Nenajdenko, V. G.
Metal-free stereoselective annulation of quinolines with trifluoroacetylacetylenes and water: an access to fluorinated oxazinoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 2268-2271
7121198 CIFC28 H19 Br2 F3 N2 O2P 1 21/n 110.054; 15.229; 17.101
90; 95.46; 90		2606Trofimov, B. A.; Belyaeva, K. V.; Nikitina, L. P.; Afonin, A. V.; Vashchenko, A. V.; Muzalevskiy, V. M.; Nenajdenko, V. G.
Metal-free stereoselective annulation of quinolines with trifluoroacetylacetylenes and water: an access to fluorinated oxazinoquinolines.
Chemical communications (Cambridge, England), 2018, 54, 2268-2271
7121199 CIFC27 H18 F4 Ir N5 O2.5I 41/a :227.885; 27.885; 12.931
90; 90; 90		10055Che, Weilong; Li, Guangfu; Liu, Xingman; Shao, Kuizhan; Zhu, Dongxia; Su, Zhongmin; Bryce, Martin R.
Selective sensing of 2,4,6-trinitrophenol (TNP) in aqueous media with "aggregation-induced emission enhancement" (AIEE)-active iridium(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 1730-1733
7121200 CIFC33 H28 F6 Ir N5 O2P -110.047; 11.116; 16.257
98.712; 104.853; 98.326		1702.4Che, Weilong; Li, Guangfu; Liu, Xingman; Shao, Kuizhan; Zhu, Dongxia; Su, Zhongmin; Bryce, Martin R.
Selective sensing of 2,4,6-trinitrophenol (TNP) in aqueous media with "aggregation-induced emission enhancement" (AIEE)-active iridium(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 1730-1733
7121201 CIFC27 H18 Cl4 Ir N5 O2P -111.546; 13.292; 13.599
109.302; 110.41; 103.766		1692Che, Weilong; Li, Guangfu; Liu, Xingman; Shao, Kuizhan; Zhu, Dongxia; Su, Zhongmin; Bryce, Martin R.
Selective sensing of 2,4,6-trinitrophenol (TNP) in aqueous media with "aggregation-induced emission enhancement" (AIEE)-active iridium(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 1730-1733
7121202 CIFC30 H22 F6 Ir N5 O3P 1 21/n 113.872; 10.096; 22.338
90; 105.767; 90		3010.8Che, Weilong; Li, Guangfu; Liu, Xingman; Shao, Kuizhan; Zhu, Dongxia; Su, Zhongmin; Bryce, Martin R.
Selective sensing of 2,4,6-trinitrophenol (TNP) in aqueous media with "aggregation-induced emission enhancement" (AIEE)-active iridium(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 1730-1733
7121203 CIFC33 H21 F4 Ir N8 O9P 1 21/n 117.161; 9.905; 23.645
90; 104.93; 90		3883.5Che, Weilong; Li, Guangfu; Liu, Xingman; Shao, Kuizhan; Zhu, Dongxia; Su, Zhongmin; Bryce, Martin R.
Selective sensing of 2,4,6-trinitrophenol (TNP) in aqueous media with "aggregation-induced emission enhancement" (AIEE)-active iridium(iii) complexes.
Chemical communications (Cambridge, England), 2018, 54, 1730-1733
7121204 CIFC29 H23 Br N2 O2C 1 2 115.6759; 10.396; 14.9375
90; 102.563; 90		2376.03Bao, Xiaoze; Wei, Shiqiang; Qu, Jingping; Wang, Baomin
C6' steric bulk of cinchona alkaloid enables an enantioselective Michael addition/annulation sequence toward pyranopyrazoles.
Chemical communications (Cambridge, England), 2018, 54, 2028-2031
7121205 CIFC17 H19 N O3 SP -15.861; 9.841; 13.802
90.674; 93.458; 92.833		793.6Chen, Jun; Guo, Hong-Mei; Zhao, Quan-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
Visible light-driven photocatalytic generation of sulfonamidyl radicals for alkene hydroamination of unsaturated sulfonamides.
Chemical communications (Cambridge, England), 2018, 54, 6780-6783
7121206 CIFC18 H21 N O4 SP 21 21 218.1382; 11.2235; 19.4636
90; 90; 90		1777.79Chen, Jun; Guo, Hong-Mei; Zhao, Quan-Qing; Chen, Jia-Rong; Xiao, Wen-Jing
Visible light-driven photocatalytic generation of sulfonamidyl radicals for alkene hydroamination of unsaturated sulfonamides.
Chemical communications (Cambridge, England), 2018, 54, 6780-6783
7121207 CIFC112 H130 Fe2 O2 P4P -112.4226; 13.5015; 16.1699
106.698; 103.359; 101.267		2425.67Heinl, S.; Timoshkin, A. Y.; Müller, J; Scheer, M.
Unexpected differences in the reactivity between the phosphorus and arsenic derivatives [(Cp<sup>BIG</sup>Fe)<sub>2</sub>(μ,η<sup>4:4</sup>-E<sub>4</sub>)] (E = P and As).
Chemical communications (Cambridge, England), 2018, 54, 2244-2247
7121208 CIFC55 H65 As5 FeP -113.4626; 13.7448; 16.0091
92.777; 114.468; 107.131		2526.71Heinl, S.; Timoshkin, A. Y.; Müller, J; Scheer, M.
Unexpected differences in the reactivity between the phosphorus and arsenic derivatives [(Cp<sup>BIG</sup>Fe)<sub>2</sub>(μ,η<sup>4:4</sup>-E<sub>4</sub>)] (E = P and As).
Chemical communications (Cambridge, England), 2018, 54, 2244-2247
7121209 CIFC110.15 H130.3 As4 Cl0.3 Fe2P b c a26.8253; 24.577; 28.7258
90; 90; 90		18938.5Heinl, S.; Timoshkin, A. Y.; Müller, J; Scheer, M.
Unexpected differences in the reactivity between the phosphorus and arsenic derivatives [(Cp<sup>BIG</sup>Fe)<sub>2</sub>(μ,η<sup>4:4</sup>-E<sub>4</sub>)] (E = P and As).
Chemical communications (Cambridge, England), 2018, 54, 2244-2247
7121210 CIFC166 H196.5 As6 Fe3 N0.5P -117.9595; 20.6577; 23.1771
98.9194; 106.184; 114.402		7152.4Heinl, S.; Timoshkin, A. Y.; Müller, J; Scheer, M.
Unexpected differences in the reactivity between the phosphorus and arsenic derivatives [(Cp<sup>BIG</sup>Fe)<sub>2</sub>(μ,η<sup>4:4</sup>-E<sub>4</sub>)] (E = P and As).
Chemical communications (Cambridge, England), 2018, 54, 2244-2247
7121211 CIFC90 H51 Cu6 Ga3 N0 O46P 63/m m c18.5324; 18.5324; 40.25
90; 90; 120		11971.8Zhang, Jian-Wei; Hu, Man-Cheng; Li, Shu-Ni; Jiang, Yu-Cheng; Qu, Peng; Zhai, Quan-Guo
Assembly of [Cu<sub>2</sub>(COO)<sub>4</sub>] and [M<sub>3</sub>(μ<sub>3</sub>-O)(COO)<sub>6</sub>] (M = Sc, Fe, Ga, and In) building blocks into porous frameworks towards ultra-high C<sub>2</sub>H<sub>2</sub>/CO<sub>2</sub> and C<sub>2</sub>H<sub>2</sub>/CH<sub>4</sub> separation performance.
Chemical communications (Cambridge, England), 2018, 54, 2012-2015
7121212 CIFC34.67 H38.33 Cl4.33 Fe2 N4 PdP 3123.629; 23.629; 16.877
90; 90; 120		8160.5Haraguchi, Ryosuke; Hoshino, Shun; Yamazaki, Tatsuro; Fukuzawa, Shin-Ichi
Chiral triazolylidene-Pd-PEPPSI: synthesis, characterization, and application in asymmetric Suzuki-Miyaura cross-coupling.
Chemical communications (Cambridge, England), 2018, 54, 2110-2113
7121213 CIFC75 H95 Cl9 N12 O32.5P 1 21 113.7293; 20.0802; 16.8259
90; 101.186; 90		4550.6Ragab, Sherif S.; Kassir, Ahmad F.; Guillot, Régis; Scherrmann, Marie-Christine; Boddaert, Thomas; Aitken, David J.
Cooperative 5- and 10-membered ring interactions in the 10-helix folding of oxetin homo-oligomers.
Chemical communications (Cambridge, England), 2018, 54, 1968-1971
7121214 CIFC29 H29 N3 O5P 1 21 18.851; 10.081; 28.437
90; 91.989; 90		2536Li, Nai-Kai; Fan, Wei-Tai; Zhang, Jun-Qi; Sun, Bing-Bing; Chen, Jun-Bo; Wang, Xing-Wang
Diastereodivergent synthesis of bispirooxindoles via asymmetric Friedel-Crafts/aldol cascade reaction: co-catalyst effects on diastereoselective outcomes.
Chemical communications (Cambridge, England), 2018, 54, 2260-2263
7121215 CIFC28 H24 Cl2 F N3 O5P 1 21/c 112.2486; 10.5812; 21.0573
90; 93.509; 90		2724Li, Nai-Kai; Fan, Wei-Tai; Zhang, Jun-Qi; Sun, Bing-Bing; Chen, Jun-Bo; Wang, Xing-Wang
Diastereodivergent synthesis of bispirooxindoles via asymmetric Friedel-Crafts/aldol cascade reaction: co-catalyst effects on diastereoselective outcomes.
Chemical communications (Cambridge, England), 2018, 54, 2260-2263
7121216 CIFC29 H29 N3 O5P 21 21 219.612; 9.9405; 52.933
90; 90; 90		5057.6Li, Nai-Kai; Fan, Wei-Tai; Zhang, Jun-Qi; Sun, Bing-Bing; Chen, Jun-Bo; Wang, Xing-Wang
Diastereodivergent synthesis of bispirooxindoles via asymmetric Friedel-Crafts/aldol cascade reaction: co-catalyst effects on diastereoselective outcomes.
Chemical communications (Cambridge, England), 2018, 54, 2260-2263
7121217 CIFC34 H58 B2 Cl6 Fe K N6 O14P -112.1407; 12.3264; 18.962
76.882; 79.997; 62.072		2434.3Voloshin, Yan Z.; Novikov, Valentin V.; Nelyubina, Yulia V.; Belov, Alexander S.; Roitershtein, Dmitrii M.; Savitsky, Anton; Mokhir, Andriy; Sutter, Jörg; Miehlich, Matthias E.; Meyer, Karsten
Synthesis and characterization of an Fe(i) cage complex with high stability towards strong H-acids.
Chemical communications (Cambridge, England), 2018, 54, 3436-3439
7121218 CIFC34 H58 B2 Cl6 Fe K N6 O14P -112.1407; 12.3264; 18.962
76.882; 79.997; 62.072		2434.3Voloshin, Yan Z.; Novikov, Valentin V.; Nelyubina, Yulia V.; Belov, Alexander S.; Roitershtein, Dmitrii M.; Savitsky, Anton; Mokhir, Andriy; Sutter, Jörg; Miehlich, Matthias E.; Meyer, Karsten
Synthesis and characterization of an Fe(i) cage complex with high stability towards strong H-acids.
Chemical communications (Cambridge, England), 2018, 54, 3436-3439
7121219 CIFC82 H94 Cl6 N2 O13P -110.6018; 17.0612; 21.6709
82; 82.577; 87.172		3847.18Arai, Kenta; Ueda, Yoshihiro; Morisaki, Kazuhiro; Furuta, Takumi; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo
Intermolecular chemo- and regioselective aromatic C-H amination of alkoxyarenes promoted by rhodium nitrenoids.
Chemical communications (Cambridge, England), 2018, 54, 2264-2267
7121220 CIFC24 H18 Cl N OP 1 21/c 111.0623; 18.5108; 9.7609
90; 98.868; 90		1974.87Hsu, Yu-Chen; Hsieh, Shu-An; Li, Po-Hsuan; Liu, Rai-Shung
Gold-catalyzed N,O-functionalization of 1,4-diyn-3-ols with N-hydroxyanilines to form highly functionalized pyrrole derivatives.
Chemical communications (Cambridge, England), 2018, 54, 2114-2117
7121221 CIFC24 H19 N OP -19.6383; 9.7333; 10.4533
80.286; 71.715; 74.791		894.5Hsu, Yu-Chen; Hsieh, Shu-An; Li, Po-Hsuan; Liu, Rai-Shung
Gold-catalyzed N,O-functionalization of 1,4-diyn-3-ols with N-hydroxyanilines to form highly functionalized pyrrole derivatives.
Chemical communications (Cambridge, England), 2018, 54, 2114-2117
7121222 CIFC20 H18 N2P b c a5.8216; 19.8873; 27.2396
90; 90; 90		3153.7Wang, Ting-Ting; Zhang, Di; Liao, Wei-Wei
Versatile synthesis of functionalized β- and γ-carbolines via Pd-catalyzed C-H addition to nitriles/cyclization sequences.
Chemical communications (Cambridge, England), 2018, 54, 2048-2051
7121223 CIFC21 H20 N2 OP -17.5703; 11.2253; 11.2607
113.159; 96.838; 101.414		841.58Wang, Ting-Ting; Zhang, Di; Liao, Wei-Wei
Versatile synthesis of functionalized β- and γ-carbolines via Pd-catalyzed C-H addition to nitriles/cyclization sequences.
Chemical communications (Cambridge, England), 2018, 54, 2048-2051
7121224 CIFC14 H16 O3P 1 21/c 121.1661; 6.9223; 23.4838
90; 91.652; 90		3439.4Viswanadh, N.; Ghotekar, Ganesh S.; Thoke, Mahesh B.; Velayudham, R.; Shaikh, Aslam C.; Karthikeyan, M.; Muthukrishnan, M.
Transition metal free regio-selective C-H hydroxylation of chromanones towards the synthesis of hydroxyl-chromanones using PhI(OAc)<sub>2</sub> as the oxidant.
Chemical communications (Cambridge, England), 2018, 54, 2252-2255
7121225 CIFC10 H12 O3P 1 21/n 17.9634; 10.2991; 11.6563
90; 91.605; 90		955.63Viswanadh, N.; Ghotekar, Ganesh S.; Thoke, Mahesh B.; Velayudham, R.; Shaikh, Aslam C.; Karthikeyan, M.; Muthukrishnan, M.
Transition metal free regio-selective C-H hydroxylation of chromanones towards the synthesis of hydroxyl-chromanones using PhI(OAc)<sub>2</sub> as the oxidant.
Chemical communications (Cambridge, England), 2018, 54, 2252-2255
7121226 CIFC21 H17 F6 N O2P -19.0952; 10.01; 10.595
95.63; 93.85; 103.51		929.3Borisova, Kseniya K.; Nikitina, Eugeniya V.; Novikov, Roman A.; Khrustalev, Victor N.; Dorovatovskii, Pavel V.; Zubavichus, Yan V.; Kuznetsov, Maxim L.; Zaytsev, Vladimir P.; Varlamov, Alexey V.; Zubkov, Fedor I.
Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.
Chemical communications (Cambridge, England), 2018, 54, 2850-2853
7121227 CIFC14 H10 F6 O2 SP 1 21/c 18.0313; 7.93; 20.946
90; 99.56; 90		1315.5Borisova, Kseniya K.; Nikitina, Eugeniya V.; Novikov, Roman A.; Khrustalev, Victor N.; Dorovatovskii, Pavel V.; Zubavichus, Yan V.; Kuznetsov, Maxim L.; Zaytsev, Vladimir P.; Varlamov, Alexey V.; Zubkov, Fedor I.
Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.
Chemical communications (Cambridge, England), 2018, 54, 2850-2853
7121228 CIFC18 H14 F9 N O4P 1 21/n 110.19; 12.17; 15.44
90; 104.72; 90		1851.9Borisova, Kseniya K.; Nikitina, Eugeniya V.; Novikov, Roman A.; Khrustalev, Victor N.; Dorovatovskii, Pavel V.; Zubavichus, Yan V.; Kuznetsov, Maxim L.; Zaytsev, Vladimir P.; Varlamov, Alexey V.; Zubkov, Fedor I.
Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.
Chemical communications (Cambridge, England), 2018, 54, 2850-2853
7121229 CIFC14 H10 F6 O2 SP -15.35; 9.655; 13.985
97.81; 98.93; 102.32		686.4Borisova, Kseniya K.; Nikitina, Eugeniya V.; Novikov, Roman A.; Khrustalev, Victor N.; Dorovatovskii, Pavel V.; Zubavichus, Yan V.; Kuznetsov, Maxim L.; Zaytsev, Vladimir P.; Varlamov, Alexey V.; Zubkov, Fedor I.
Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.
Chemical communications (Cambridge, England), 2018, 54, 2850-2853
7121230 CIFC16 H10 F9 N O3P 1 21/c 111.47; 18.01; 17.04
90; 108.15; 90		3344.9Borisova, Kseniya K.; Nikitina, Eugeniya V.; Novikov, Roman A.; Khrustalev, Victor N.; Dorovatovskii, Pavel V.; Zubavichus, Yan V.; Kuznetsov, Maxim L.; Zaytsev, Vladimir P.; Varlamov, Alexey V.; Zubkov, Fedor I.
Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.
Chemical communications (Cambridge, England), 2018, 54, 2850-2853
7121231 CIFC21 H17 F6 N O2P c a 2118.903; 5.5733; 36.08
90; 90; 90		3801.1Borisova, Kseniya K.; Nikitina, Eugeniya V.; Novikov, Roman A.; Khrustalev, Victor N.; Dorovatovskii, Pavel V.; Zubavichus, Yan V.; Kuznetsov, Maxim L.; Zaytsev, Vladimir P.; Varlamov, Alexey V.; Zubkov, Fedor I.
Diels-Alder reactions between hexafluoro-2-butyne and bis-furyl dienes: kinetic versus thermodynamic control.
Chemical communications (Cambridge, England), 2018, 54, 2850-2853
7121232 CIFC210 H208 F18 N96 O60 Pt4 S6P -118.9989; 19.6522; 20.0079
89.782; 80.632; 88.26		7367.3Kuang, Shengjian; Hu, Zhixiong; Zhang, Hao; Zhang, Xiongzhi; Liang, Feng; Zhao, Zhiyong; Liu, Simin
Enhancement of metal-metal interactions inside a large-cavity synthetic host in water.
Chemical communications (Cambridge, England), 2018, 54, 2169-2172
7121234 CIFC47.5 H41 F3 N2 O TiP -19.83402; 10.87734; 19.1786
104.504; 103.273; 91.6813		1924.83Foschi, Francesco; Roth, Torsten; Enders, Markus; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H.
Isolation and structural characterization of a titanacyclopropane as key intermediate in the double aryl Grignard addition to 2-(arylethynyl)pyridine derivatives.
Chemical communications (Cambridge, England), 2018, 54, 2228-2231
7121235 CIFC24 H16 F2 N2P 3228.9605; 28.9605; 5.6946
90; 90; 120		4136.2Foschi, Francesco; Roth, Torsten; Enders, Markus; Wadepohl, Hubert; Clot, Eric; Gade, Lutz H.
Isolation and structural characterization of a titanacyclopropane as key intermediate in the double aryl Grignard addition to 2-(arylethynyl)pyridine derivatives.
Chemical communications (Cambridge, England), 2018, 54, 2228-2231

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