Crystallography Open Database

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7238987 CIFC16 H14 N2 OP 1 21/n 113.427; 5.6126; 16.7627
90; 91.685; 90
1262.7Rao, D. Nageswar; Rasheed, Sk.; Aravinda, S.; Vishwakarma, Ram A.; Das, Parthasarathi
Base and ligand free copper-catalyzed N-arylation of 2-amino-N-heterocycles with boronic acids in air
RSC Advances, 2013, 3, 11472
7238988 CIFC19 H25 N9 O8P -110.8173; 11.0856; 13.235
89.971; 69.525; 63.586
1308.7Radhakrishnan, K.; Burgula, Laxmi Narayana; Kundu, Lal Mohan
Watson‒Crick and Hoogsteen tri-base pairing: a co-crystal structure of a 2 : 1 complex of 6-isopropyluracil and adenine nucleobases
RSC Advances, 2013, 3, 7282
7238989 CIFC9 H12 Cd Cl2 N4 SP 1 21/n 18.9957; 13.855; 11.033
90; 90.941; 90
1374.9Manikandan, Rajendran; Chitrapriya, Nataraj; Jang, Yoon Jung; Viswanathamurthi, Periasamy
Evaluation of DNA-binding, radical scavenging and cytotoxic activity of five coordinated Cd(ii) complexes containing 2-acetylpyridine-N4-substituted thiosemicarbazone
RSC Advances, 2013, 3, 11647
7238990 CIFC16 H14 O4P -17.119; 7.462; 12.573
76.093; 85.589; 73.234
620.74Petrov, Vesselin; Diniz, Ana Marta; Cunha-Silva, Luís; Parola, A. Jorge; Pina, Fernando
Kinetic and thermodynamic study of 2′-hydroxy-8-methoxyflavylium. Reaction network interconverting flavylium cation and flavanone
RSC Advances, 2013, 3, 10786
7238991 CIFC28 H28 N2 O9P 1 21/c 118.8356; 9.5741; 15.4158
90; 103.78; 90
2699.98Tan, Wei; Zhu, Xiao-Tong; Zhang, Shu; Xing, Gui-Juan; Zhu, Ren-Yi; Shi, Feng
Diversity-oriented synthesis of spiro-oxindole-based 2,5-dihydropyrroles via three-component cycloadditions and evaluation on their cytotoxicity
RSC Advances, 2013, 3, 10875
7238992 CIFC17 H14 N4 SP 1 21 19.5334; 6.4275; 13.057
90; 108.293; 90
759.65Basu, Arghya; Thiyagarajan, Durairaj; Kar, Chirantan; Ramesh, Aiyagari; Das, Gopal
Synthesis, crystal structure and bio-macromolecular interaction studies of pyridine-based thiosemicarbazone and its Ni(ii) and Cu(ii) complexes
RSC Advances, 2013, 3, 14088
7238993 CIFC37 H33 N9 Ni O S2P 1 21 19.0267; 33.436; 12.2036
90; 100.916; 90
3616.6Basu, Arghya; Thiyagarajan, Durairaj; Kar, Chirantan; Ramesh, Aiyagari; Das, Gopal
Synthesis, crystal structure and bio-macromolecular interaction studies of pyridine-based thiosemicarbazone and its Ni(ii) and Cu(ii) complexes
RSC Advances, 2013, 3, 14088
7238994 CIFC17 H13 Cl Cu N4 SP 1 21/c 17.5413; 13.9846; 15.6339
90; 101.29; 90
1616.88Basu, Arghya; Thiyagarajan, Durairaj; Kar, Chirantan; Ramesh, Aiyagari; Das, Gopal
Synthesis, crystal structure and bio-macromolecular interaction studies of pyridine-based thiosemicarbazone and its Ni(ii) and Cu(ii) complexes
RSC Advances, 2013, 3, 14088
7238995 CIFC22 H24 O5P -18.6741; 9.1126; 12.8419
96.627; 102.887; 106.395
931.84Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7238996 CIFC23 H26 O5P 1 21/c 112.6354; 10.1017; 15.6517
90; 95.22; 90
1989.5Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7238997 CIFC20 H20 O5P 1 21/n 19.5864; 12.2835; 14.5863
90; 97.979; 90
1701Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7238998 CIFC20 H20 O5P 1 21/c 120.44; 10.579; 7.873
90; 92.119; 90
1701.3Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7238999 CIFC24 H28 O5P -18.4362; 10.6638; 12.5335
76.146; 79.366; 84.811
1074.7Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7239000 CIFC23 H26 O5P 1 21/n 112.4423; 12.3999; 13.5967
90; 97.19; 90
2081.2Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7239001 CIFC27 H34 O5P 1 21/c 112.518; 8.3814; 23.699
90; 103.33; 90
2419.5Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7239002 CIFC23 H26 O5P 21 21 2112.1101; 12.3001; 13.492
90; 90; 90
2009.7Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7239003 CIFC23 H26 O5C 1 2/c 125.1535; 8.7953; 36.307
90; 96.419; 90
7981.9Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7239004 CIFC22 H24 O5P 1 21/n 115.8167; 8.221; 15.9694
90; 116.312; 90
1861.3Basavaiah, Deevi; Kumar, Katta Santosh; Aravindu, Kunche; Lingaiah, Balthu
The Baylis‒Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
RSC Advances, 2013, 3, 9629
7239005 CIFC10 H9 N3 O4P -17.343; 12.189; 12.8943
70.277; 87.489; 81.431
1074.23Ramesh, Samikannu; Arunachalam, Pirama Nayagam; Lalitha, Appaswami
Regioselective ethoxy-carbonylation of indoles and indazoles using DEAD and tetraethylammonium cyanide
RSC Advances, 2013, 3, 8666
7239006 CIFC11 H13 N O SP 21 21 219.5407; 8.005; 6.7851
90; 90; 90
1061.35Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack
RSC Advances, 2013, 3, 24997
7239007 CIFC9 H15 N O3 SP 1 21/a 17.4816; 15.2728; 9.6621
90; 97.115; 90
1095.54Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack
RSC Advances, 2013, 3, 24997
7239008 CIFC9 H15 N O4P b c a9.1981; 9.2778; 23.4543
90; 90; 90
2001.55Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack
RSC Advances, 2013, 3, 24997
7239009 CIFC9 H15 N O3 SP 1 21/n 19.6972; 6.7661; 17.4884
90; 100.177; 90
1129.4Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack
RSC Advances, 2013, 3, 24997
7239010 CIFC13 H25 N O3 SP 1 21/c 111.4804; 9.954; 28.7919
90; 90; 90
3290.22Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack
RSC Advances, 2013, 3, 24997
7239011 CIFC11 H22 N2 O3 SP 1 21/c 113.1321; 11.0452; 10.1525
90; 100.532; 90
1447.78Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack
RSC Advances, 2013, 3, 24997
7239012 CIFC16 H30 N2 O5 SP 1 21/n 15.9611; 19.2487; 17.6222
90; 94.909; 90
2014.61Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack
RSC Advances, 2013, 3, 24997
7239013 CIFC13 H28 N2 O3P 1 21/c 112.2603; 12.7294; 10.9082
90; 110.413; 90
1595.5Wang, Hui; Gurau, Gabriela; Kelley, Steven P.; Myerson, Allan S.; Rogers, Robin D.
Hydrophobic vs. hydrophilic ionic liquid separations strategies in support of continuous pharmaceutical manufacturing
RSC Advances, 2013, 3, 10019
7239014 CIFC11 H10 Cl0 O2 SP 1 21/n 19.1727; 12.4922; 15.7956
90; 104.861; 90
1749.4Shukla, Gaurav; Verma, Girijesh Kumar; Nagaraju, Anugula; Verma, Rajiv Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar
DMAP mediated one-pot domino thienannulation: a versatile, regioselective and green mechanochemical route to naphtho[2,3-b]thiophenes
RSC Advances, 2013, 3, 13811
7239015 CIFC18 H10 O3 S3P -18.245; 8.504; 12.515
97.9; 92.639; 113.007
795.2Shukla, Gaurav; Verma, Girijesh Kumar; Nagaraju, Anugula; Verma, Rajiv Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar
DMAP mediated one-pot domino thienannulation: a versatile, regioselective and green mechanochemical route to naphtho[2,3-b]thiophenes
RSC Advances, 2013, 3, 13811
7239016 CIFC18 H17 N O3 SP -16.1217; 11.429; 11.589
85.145; 83.541; 80.709
793.3Shukla, Gaurav; Verma, Girijesh Kumar; Nagaraju, Anugula; Verma, Rajiv Kumar; Raghuvanshi, Keshav; Singh, Maya Shankar
DMAP mediated one-pot domino thienannulation: a versatile, regioselective and green mechanochemical route to naphtho[2,3-b]thiophenes
RSC Advances, 2013, 3, 13811
7239017 CIFC71 H47 Cl2 N17 O8 Ru2P 1 21/c 125.197; 12.849; 25.351
90; 105.04; 90
7926Saha, Debasish; Das, Shyamal; Karmakar, Srikanta; Dutta, Supriya; Baitalik, Sujoy
Synthesis, structural characterization and anion-, cation- and solvent-induced tuning of photophysical properties of a bimetallic Ru(ii) complex: combined experimental and DFT/TDDFT investigation
RSC Advances, 2013, 3, 17314
7239018 CIFC27 H26 N2 O6C 1 2/c 121.75; 9.476; 24.315
90; 101.661; 90
4908Huang, Lan; Su, Jingru; Zhong, Desheng; Wang, Haibo; Liu, Ruiyuan; Yu, Le; Zhu, Qiuhua; Liu, Shuwen
Copper-induced fluorescence enhancement and particle-size decrease of a C-6 unsubstituted tetrahydropyrimidine racemate
RSC Advances, 2013, 3, 13286
7239019 CIFC23 H15 Cl N2 O5P 1 21 15.9139; 18.664; 8.834
90; 93.314; 90
973.4Ma, Shijun; Wu, Lulu; Liu, Ming; Xu, Xiufang; Huang, Yaodong; Wang, Yongmei
Highly enantioselective aza-Michael addition reactions of 4-nitrophthalimide with α,β-unsaturated ketones
RSC Advances, 2013, 3, 11498
7239020 CIFC28 H20 OP 1 21/n 111.3616; 11.6419; 14.837
90; 96.197; 90
1951Teng, Ming-yu; Liu, Ying; Li, Shao-lu; Huang, Guoli; Jiang, Juli; Wang, Leyong
Synthesis, chemo-selective properties of substituted 9-aryl-9H-fluorenes from triarylcarbinols and enantiomerical kinetics of chiral 9-methoxy-11-(naphthalen-1-yl)-11H-benzo[a]fluorene
RSC Advances, 2013, 3, 9016
7239021 CIFC27 H18P -112.975; 7.2022; 19.2
90; 94.338; 90
1789.1Teng, Ming-yu; Liu, Ying; Li, Shao-lu; Huang, Guoli; Jiang, Juli; Wang, Leyong
Synthesis, chemo-selective properties of substituted 9-aryl-9H-fluorenes from triarylcarbinols and enantiomerical kinetics of chiral 9-methoxy-11-(naphthalen-1-yl)-11H-benzo[a]fluorene
RSC Advances, 2013, 3, 9016
7239022 CIFC22 H20 O3P 1 21/c 115.412; 5.8149; 19.488
90; 96.633; 90
1734.8Teng, Ming-yu; Liu, Ying; Li, Shao-lu; Huang, Guoli; Jiang, Juli; Wang, Leyong
Synthesis, chemo-selective properties of substituted 9-aryl-9H-fluorenes from triarylcarbinols and enantiomerical kinetics of chiral 9-methoxy-11-(naphthalen-1-yl)-11H-benzo[a]fluorene
RSC Advances, 2013, 3, 9016
7239023 CIFC25 H20 O2P 1 21/n 110.533; 6.5954; 26.832
90; 97.565; 90
1847.8Teng, Ming-yu; Liu, Ying; Li, Shao-lu; Huang, Guoli; Jiang, Juli; Wang, Leyong
Synthesis, chemo-selective properties of substituted 9-aryl-9H-fluorenes from triarylcarbinols and enantiomerical kinetics of chiral 9-methoxy-11-(naphthalen-1-yl)-11H-benzo[a]fluorene
RSC Advances, 2013, 3, 9016
7239024 CIFC23 H17 Cl4 Fe OP b c n10.949; 17.19; 12.099
90; 90; 90
2277.2Ye, Junwei; Zhang, Xiangdong; Deng, Dai; Ning, Guiling; Liu, Tianqing; Zhuang, Meiling; Yang, Lijian; Gong, Weitao; Lin, Yuan
Selective C‒C bond cleavage of cyclopentadiene rings assisted by ferric chloride to synthesize water-soluble pyrylium salts
RSC Advances, 2013, 3, 8232
7239025 CIFC24 H19 Cl4 Fe O2P b c a13.319; 18.375; 19.555
90; 90; 90
4786Ye, Junwei; Zhang, Xiangdong; Deng, Dai; Ning, Guiling; Liu, Tianqing; Zhuang, Meiling; Yang, Lijian; Gong, Weitao; Lin, Yuan
Selective C‒C bond cleavage of cyclopentadiene rings assisted by ferric chloride to synthesize water-soluble pyrylium salts
RSC Advances, 2013, 3, 8232
7239026 CIFC25 H21 Cl4 Fe O3P 1 21/n 17.542; 18.02; 19.28
90; 96.98; 90
2601Ye, Junwei; Zhang, Xiangdong; Deng, Dai; Ning, Guiling; Liu, Tianqing; Zhuang, Meiling; Yang, Lijian; Gong, Weitao; Lin, Yuan
Selective C‒C bond cleavage of cyclopentadiene rings assisted by ferric chloride to synthesize water-soluble pyrylium salts
RSC Advances, 2013, 3, 8232
7239027 CIFC26 H23 Cl4 Fe O4P 1 21/c 17.772; 19.769; 17.515
90; 92.98; 90
2687Ye, Junwei; Zhang, Xiangdong; Deng, Dai; Ning, Guiling; Liu, Tianqing; Zhuang, Meiling; Yang, Lijian; Gong, Weitao; Lin, Yuan
Selective C‒C bond cleavage of cyclopentadiene rings assisted by ferric chloride to synthesize water-soluble pyrylium salts
RSC Advances, 2013, 3, 8232
7239028 CIFC29 H25 Cl4 Fe O3P 1 21/c 110.487; 32.446; 9.5526
90; 107.715; 90
3096.3Ye, Junwei; Zhang, Xiangdong; Deng, Dai; Ning, Guiling; Liu, Tianqing; Zhuang, Meiling; Yang, Lijian; Gong, Weitao; Lin, Yuan
Selective C‒C bond cleavage of cyclopentadiene rings assisted by ferric chloride to synthesize water-soluble pyrylium salts
RSC Advances, 2013, 3, 8232
7239029 CIFC15 H13 N O3 SP 1 21/c 112.5933; 15.1264; 15.0649
90; 111.798; 90
2664.5Patpi, Santhosh Reddy; Sridhar, Balasubramanian; Tadikamalla, Prabhakar Rao; Kantevari, Srinivas
Pd-catalyzed site selective C‒H acetoxylation of aryl/heteroaryl/thiophenyl tethered dihydroquinolinones
RSC Advances, 2013, 3, 10251
7239030 CIFC25 H23 N O3P 1 21/c 116.2313; 15.4503; 8.0772
90; 96.738; 90
2011.6Patpi, Santhosh Reddy; Sridhar, Balasubramanian; Tadikamalla, Prabhakar Rao; Kantevari, Srinivas
Pd-catalyzed site selective C‒H acetoxylation of aryl/heteroaryl/thiophenyl tethered dihydroquinolinones
RSC Advances, 2013, 3, 10251
7239031 CIFC28 H20 OC 1 2/c 125.7493; 8.1753; 21.7304
90; 117.408; 90
4061Cai, Ranran; Huang, Mengmeng; Cui, Xiuling; Zhang, Jianye; Du, Chenxia; Wu, Yusheng; Wu, Yangjie
Synthesis of cyclopentadienyl alkyl ethers via Pd-catalyzed cyclotrimerization of diarylacetylenes
RSC Advances, 2013, 3, 13140
7239032 CIFC41 H38 OP 1 21/c 119.936; 7.9365; 25.6157
90; 127.958; 90
3195.6Cai, Ranran; Huang, Mengmeng; Cui, Xiuling; Zhang, Jianye; Du, Chenxia; Wu, Yusheng; Wu, Yangjie
Synthesis of cyclopentadienyl alkyl ethers via Pd-catalyzed cyclotrimerization of diarylacetylenes
RSC Advances, 2013, 3, 13140
7239033 CIFC36 H28 OP -110.131; 10.15; 14.682
99.93; 93.55; 114.56
1337.5Cai, Ranran; Huang, Mengmeng; Cui, Xiuling; Zhang, Jianye; Du, Chenxia; Wu, Yusheng; Wu, Yangjie
Synthesis of cyclopentadienyl alkyl ethers via Pd-catalyzed cyclotrimerization of diarylacetylenes
RSC Advances, 2013, 3, 13140
7239034 CIFC20 H20 N2 O2P 1 21/c 18.2474; 17.675; 11.501
90; 101.32; 90
1643.9Long, Lingliang; Li, Xiufen; Zhang, Dongdong; Meng, Suci; Zhang, Jinfang; Sun, Xianglan; Zhang, Chi; Zhou, Liping; Wang, Lin
Amino-coumarin based fluorescence ratiometric sensors for acidic pH and their application for living cells imaging
RSC Advances, 2013, 3, 12204
7239035 CIFC21 H27 N O5P 21 21 217.6964; 9.0385; 28.1815
90; 90; 90
1960.4Savić, Marina P.; Djurendić, Evgenija A.; Petri, Edward T.; Ćelić, Andjelka; Klisurić, Olivera R.; Sakač, Marija N.; Jakimov, Dimitar S.; Kojić, Vesna V.; Gaši, Katarina M. Penov
Synthesis, structural analysis and antiproliferative activity of some novel D-homo lactone androstane derivatives
RSC Advances, 2013, 3, 10385
7239036 CIFC19 H27 N O5P 21 21 217.6411; 8.3284; 27.4713
90; 90; 90
1748.22Savić, Marina P.; Djurendić, Evgenija A.; Petri, Edward T.; Ćelić, Andjelka; Klisurić, Olivera R.; Sakač, Marija N.; Jakimov, Dimitar S.; Kojić, Vesna V.; Gaši, Katarina M. Penov
Synthesis, structural analysis and antiproliferative activity of some novel D-homo lactone androstane derivatives
RSC Advances, 2013, 3, 10385
7239037 CIFC20 H17 N2 O5P 1 21/c 19.0098; 11.0194; 18.008
90; 101.284; 90
1753.3Jaiswal, Pradeep Kumar; Biswas, Soumen; Singh, Shivendra; Pathak, Biswarup; Mobin, Shaikh M.; Samanta, Sampak
Stereoselective synthesis of highly functionalized tetrahydrocarbazoles through a domino Michael‒Henry reaction: an easy access to four contiguous chiral centers
RSC Advances, 2013, 3, 10644
7239038 CIFC20 H18 N2 O5P 1 21/n 18.876; 11.1516; 17.9923
90; 104.062; 90
1727.54Jaiswal, Pradeep Kumar; Biswas, Soumen; Singh, Shivendra; Pathak, Biswarup; Mobin, Shaikh M.; Samanta, Sampak
Stereoselective synthesis of highly functionalized tetrahydrocarbazoles through a domino Michael‒Henry reaction: an easy access to four contiguous chiral centers
RSC Advances, 2013, 3, 10644
7239039 CIFC48 H48 Cu N6 O8P 1 21 19.95; 13.482; 17.253
90; 105.438; 90
2230.9Samanta, Suvendu; Das, Sudipto; Samanta, Partha Kumar; Dutta, Supriya; Biswas, Papu
A mononuclear copper(ii) complex immobilized in mesoporous silica: an efficient heterogeneous catalyst for the aerobic oxidation of benzylic alcohols
RSC Advances, 2013, 3, 19455
7239040 CIFC19 H24 Cu N10 S2P -19.469; 10.956; 12.77
70.023; 68.5; 87.844
1152.6Wang, Xuan; Xing, Yong Heng; Bai, Feng Ying; Wang, Xin Yu; Guan, Qing Lin; Hou, Ya Nan; Zhang, Rui; Shi, Zhan
Synthesis, structure, and surface photovoltage properties of a series of novel d7‒d10 metal complexes with pincer N-heterocycle ligands
RSC Advances, 2013, 3, 16021
7239041 CIFC19 H24 N10 Ni S2P -18.8512; 11.923; 13.48
65.61; 89.96; 70.44
1205.1Wang, Xuan; Xing, Yong Heng; Bai, Feng Ying; Wang, Xin Yu; Guan, Qing Lin; Hou, Ya Nan; Zhang, Rui; Shi, Zhan
Synthesis, structure, and surface photovoltage properties of a series of novel d7‒d10 metal complexes with pincer N-heterocycle ligands
RSC Advances, 2013, 3, 16021
7239042 CIFC19 H24 Co N10 S2P -17.7012; 11.514; 14.198
85.868; 75.758; 86.508
1215.9Wang, Xuan; Xing, Yong Heng; Bai, Feng Ying; Wang, Xin Yu; Guan, Qing Lin; Hou, Ya Nan; Zhang, Rui; Shi, Zhan
Synthesis, structure, and surface photovoltage properties of a series of novel d7‒d10 metal complexes with pincer N-heterocycle ligands
RSC Advances, 2013, 3, 16021
7239043 CIFC17 H26 N14 Ni OP 1 21/c 113.9708; 15.4535; 11.0815
90; 106.174; 90
2297.8Wang, Xuan; Xing, Yong Heng; Bai, Feng Ying; Wang, Xin Yu; Guan, Qing Lin; Hou, Ya Nan; Zhang, Rui; Shi, Zhan
Synthesis, structure, and surface photovoltage properties of a series of novel d7‒d10 metal complexes with pincer N-heterocycle ligands
RSC Advances, 2013, 3, 16021
7239044 CIFC17 H24 Co N14C 1 2/c 116.86; 11.386; 11.379
90; 95.365; 90
2174.8Wang, Xuan; Xing, Yong Heng; Bai, Feng Ying; Wang, Xin Yu; Guan, Qing Lin; Hou, Ya Nan; Zhang, Rui; Shi, Zhan
Synthesis, structure, and surface photovoltage properties of a series of novel d7‒d10 metal complexes with pincer N-heterocycle ligands
RSC Advances, 2013, 3, 16021
7239045 CIFC16 H19 N O2C 1 2/c 122.219; 7.2701; 19.4157
90; 117.964; 90
2770.1Lei, Shenghui
Synthetic studies towards the Lycopodium alkaloid paniculatine
RSC Advances, 2013, 3, 11014
7239046 CIFC24 H29 N O3P 1 21/n 112.8516; 9.598; 17.1017
90; 98.929; 90
2083.92Lei, Shenghui
Synthetic studies towards the Lycopodium alkaloid paniculatine
RSC Advances, 2013, 3, 11014
7239047 CIFC17 H26 Cl N O3P 1 21/c 112.523; 9.641; 14.152
90; 102.01; 90
1671.23Lei, Shenghui
Synthetic studies towards the Lycopodium alkaloid paniculatine
RSC Advances, 2013, 3, 11014
7239048 CIFC20 H28 OP -16.8754; 10.7487; 11.7991
91.303; 92.041; 99.15
859.97Kakde, Badrinath N.; De, Subhadip; Dey, Dhananjay; Bisai, Alakesh
Metal triflate-catalyzed cyclization of arylvinylcarbinols: formal synthesis of (±)-dichroanone and (±)-taiwaniaquinone H
RSC Advances, 2013, 3, 8176
7239049 CIFC18 H22 O3P 1 21/n 18.0057; 19.331; 9.6263
90; 95.807; 90
1482.1Kakde, Badrinath N.; De, Subhadip; Dey, Dhananjay; Bisai, Alakesh
Metal triflate-catalyzed cyclization of arylvinylcarbinols: formal synthesis of (±)-dichroanone and (±)-taiwaniaquinone H
RSC Advances, 2013, 3, 8176
7239050 CIFC19 H27 N3 O4P -19.524; 9.968; 10.582
96.259; 102.562; 90.735
974Joseph, Nayana; Rajan, Rani; John, Jubi; Devika, N. V.; Chand, S. Sarath; Suresh, E.; Pihko, Petri M.; Radhakrishnan, K. V.
An exclusive approach to 3,4-disubstituted cyclopentenes and alkylidene cyclopentenes via the palladium catalyzed ring opening of azabicyclic olefins with aryl halides
RSC Advances, 2013, 3, 7751
7239051 CIFC19 H14 Br N3 O3P -17.8668; 15.1461; 15.4604
77.883; 89.983; 78
1759.92Sivakumar, Sathiyamoorthi; Kanchithalaivan, Selvaraj; Kumar, Raju Ranjith
A one-pot three-component domino protocol for the synthesis of penta-substituted 4H-pyrans
RSC Advances, 2013, 3, 13357
7239052 CIFC20 H30 O3P 21 21 216.77744; 14.074; 19.0348
90; 90; 90
1815.65Ramachary, Dhevalapally B.; Sakthidevi, Rajasekar; Reddy, P. Srinivasa
Direct organocatalytic stereoselective transfer hydrogenation of conjugated olefins of steroids
RSC Advances, 2013, 3, 13497
7239053 CIFC19 H28 O2P 21 21 217.9253; 8.4074; 25.074
90; 90; 90
1670.7Ramachary, Dhevalapally B.; Sakthidevi, Rajasekar; Reddy, P. Srinivasa
Direct organocatalytic stereoselective transfer hydrogenation of conjugated olefins of steroids
RSC Advances, 2013, 3, 13497
7239054 CIFC36 H92 Ce2 Cl2 O20 Ti4P 1 21/n 111.9651; 19.467; 12.9495
90; 91.992; 90
3014.4Lv, Yaokang; Yao, Mingming; Holgado, Juan Pedro; Roth, Torsten; Steiner, Alexander; Gan, Lihua; Lambert, Richard M.; Wright, Dominic S.
A low-temperature single-source route to an efficient broad-band cerium(iii) photocatalyst using a bimetallic polyoxotitanium cage
RSC Advances, 2013, 3, 13659
7239055 CIFC44 H110 Ce O29 Ti8C 1 2/c 115.63; 23.318; 20.732
90; 93.994; 90
7538Lv, Yaokang; Yao, Mingming; Holgado, Juan Pedro; Roth, Torsten; Steiner, Alexander; Gan, Lihua; Lambert, Richard M.; Wright, Dominic S.
A low-temperature single-source route to an efficient broad-band cerium(iii) photocatalyst using a bimetallic polyoxotitanium cage
RSC Advances, 2013, 3, 13659
7239056 CIFC18 H21 N3 O2 SP 1 21/n 18.8513; 16.517; 11.4378
90; 94.84; 90
1666.21Chen, Li-Hsun; Chuang, Ying-Sheng; Narhe, Bharat D.; Sun, Chung-Ming
A concise synthesis of 2-(2-aminothiophene)-benzimidazoles by one-pot multicomponent reaction
RSC Advances, 2013, 3, 13934
7239057 CIFC22 H20 N4 O2P 1 21/c 121.059; 11.2828; 15.679
90; 95.888; 90
3705.7Yu, Fuchao; Chen, Zhiqiong; Hao, Xiaopan; Jiang, Xiuyang; Yan, Shengjiao; Lin, Jun
Three component solvent-free synthesis of 1H-pyrazol-5(4H)-one-based heterocyclic ketene aminal derivatives
RSC Advances, 2013, 3, 13183
7239058 CIFC16 H25 Cu4 N12 O41 P W12C 1 2/m 112.774; 19.299; 11.056
90; 98.752; 90
2693.8Tian, AiXiang; Lin, XiaoLing; Liu, XiaoJing; Ying, Jun; Wang, XiuLi
Hydroxyl- and chloro-bridges as “structural assistants” in the construction of two new Keggin-based 3D frameworks
RSC Advances, 2013, 3, 17188
7239059 CIFC32 H54 Cl Cu2 N24 O43 P W12P -112.067; 15.262; 20.31
96.457; 95.796; 90.465
3697Tian, AiXiang; Lin, XiaoLing; Liu, XiaoJing; Ying, Jun; Wang, XiuLi
Hydroxyl- and chloro-bridges as “structural assistants” in the construction of two new Keggin-based 3D frameworks
RSC Advances, 2013, 3, 17188
7239060 CIFC16 H12 N2 O2 SP n a 219.88; 22.9781; 6.1558
90; 90; 90
1397.51Tiwari, Karishma; Mishra, Monika; Singh, Vinod P.
A highly sensitive and selective fluorescent sensor for Al3+ ions based on thiophene-2-carboxylic acid hydrazide Schiff base
RSC Advances, 2013, 3, 12124
7239061 CIFC19 H21 Br N2 O3P 21 21 214.9215; 13.8042; 26.079
90; 90; 90
1771.7Maurya, Hardesh K.; Vasudev, Prema G.; Gupta, Atul
A regioselective synthesis of 2,6-diarylpyridines
RSC Advances, 2013, 3, 12955
7239062 CIFC40 H36 F9 Nd O14P 1 21/c 113.228; 12.583; 26.182
90; 108.3; 90
4138Li, Weizuo; Yan, Pengfei; Hou, Guangfeng; Li, Hongfeng; Li, Guangming
Near-infrared luminescent hybrid materials ‒ PMMA doped with a neodymium complex: synthesis, structure and photophysical properties
RSC Advances, 2013, 3, 18173
7239063 CIFC41 H40 Cl4 F9 O15 YbP -111.777; 12.332; 18.168
78.47; 88.87; 70.05
2426.8Li, Weizuo; Yan, Pengfei; Hou, Guangfeng; Li, Hongfeng; Li, Guangming
Near-infrared luminescent hybrid materials ‒ PMMA doped with a neodymium complex: synthesis, structure and photophysical properties
RSC Advances, 2013, 3, 18173
7239064 CIFC51 H38 F9 N2 Nd O12P 1 21/c 113.3522; 19.6431; 19.7333
90; 106.942; 90
4951Li, Weizuo; Yan, Pengfei; Hou, Guangfeng; Li, Hongfeng; Li, Guangming
Near-infrared luminescent hybrid materials ‒ PMMA doped with a neodymium complex: synthesis, structure and photophysical properties
RSC Advances, 2013, 3, 18173
7239065 CIFC13 H11 F3 O4P -18.4438; 11.4961; 13.5973
103.513; 96.609; 95.597
1264.21Li, Weizuo; Yan, Pengfei; Hou, Guangfeng; Li, Hongfeng; Li, Guangming
Near-infrared luminescent hybrid materials ‒ PMMA doped with a neodymium complex: synthesis, structure and photophysical properties
RSC Advances, 2013, 3, 18173
7239069 CIFC46 H50 N8 Ni O2 S4P -18.1895; 8.5987; 16.7988
92.215; 102.812; 105.961
1102.75Yang, Xiong-Bo; Zhou, Li; Huang, Long-Biao; Xu, Jia-Ju; Zhou, Ye; Han, Su-Ting; Xu, Zong-Xiang; Lau, Victor C. Y.; Hon-Wah Lam, Micheal; Wong, Wai-Yeung; Roy, V. A. L.
Importance of alkyl chain-length on the self-assembly of new Ni(qdt)2 complexes and charge transport properties
RSC Advances, 2013, 3, 12075
7239070 CIFC48 H50 N8 Ni S4P 1 21/c 114.8356; 10.8116; 13.3564
90; 93.711; 90
2137.83Yang, Xiong-Bo; Zhou, Li; Huang, Long-Biao; Xu, Jia-Ju; Zhou, Ye; Han, Su-Ting; Xu, Zong-Xiang; Lau, Victor C. Y.; Hon-Wah Lam, Micheal; Wong, Wai-Yeung; Roy, V. A. L.
Importance of alkyl chain-length on the self-assembly of new Ni(qdt)2 complexes and charge transport properties
RSC Advances, 2013, 3, 12075
7239071 CIFC50 H58 N8 Ni O2 S4P 1 21/c 115.263; 9.2809; 16.8903
90; 93.097; 90
2389.09Yang, Xiong-Bo; Zhou, Li; Huang, Long-Biao; Xu, Jia-Ju; Zhou, Ye; Han, Su-Ting; Xu, Zong-Xiang; Lau, Victor C. Y.; Hon-Wah Lam, Micheal; Wong, Wai-Yeung; Roy, V. A. L.
Importance of alkyl chain-length on the self-assembly of new Ni(qdt)2 complexes and charge transport properties
RSC Advances, 2013, 3, 12075
7239072 CIFC11 H10 Br N3 OP 21 21 215.6282; 9.0457; 22.768
90; 90; 90
1159.1Li, Nai-Kai; Liu, Zhao-Min; Huang, Xiao-Fei; Zhang, Jin-Xin; Chen, Xiang; Wang, Yong; Wang, Xing-Wang
Enantioselective Strecker-type reaction between azomethine imines and trimethylsilyl cyanide catalyzed by a cinchona alkaloid-derived thiourea bearing multiple hydrogen-bonding donors
RSC Advances, 2013, 3, 9154
7239073 CIFC11 H10 Br N3 OP 15.5927; 9.9073; 11.448
113.882; 91.874; 99.063
569.49Li, Nai-Kai; Liu, Zhao-Min; Huang, Xiao-Fei; Zhang, Jin-Xin; Chen, Xiang; Wang, Yong; Wang, Xing-Wang
Enantioselective Strecker-type reaction between azomethine imines and trimethylsilyl cyanide catalyzed by a cinchona alkaloid-derived thiourea bearing multiple hydrogen-bonding donors
RSC Advances, 2013, 3, 9154
7239074 CIFC40 H26 N2P 1 21/c 116.4103; 10.588; 16.0074
90; 94.814; 90
2771.51Chen, Chien-Tien; Chao, Wei-Shan; Liu, Hao-Wei; Wei, Yi; Jou, Jwo-Huei; Kumar, Sudhir
Spirally configured cis-stilbene/fluorene hybrids as ambipolar, fluorescent materials for organic light emitting diode applications
RSC Advances, 2013, 3, 9381
7239075 CIFC46 H30 N2C 1 2/c 133.6125; 8.5624; 26.3251
90; 116.544; 90
6777.8Chen, Chien-Tien; Chao, Wei-Shan; Liu, Hao-Wei; Wei, Yi; Jou, Jwo-Huei; Kumar, Sudhir
Spirally configured cis-stilbene/fluorene hybrids as ambipolar, fluorescent materials for organic light emitting diode applications
RSC Advances, 2013, 3, 9381
7239076 CIFC52 H35 N3P 1 21/a 110.7889; 19.9049; 17.5852
90; 106.621; 90
3618.67Chen, Chien-Tien; Chao, Wei-Shan; Liu, Hao-Wei; Wei, Yi; Jou, Jwo-Huei; Kumar, Sudhir
Spirally configured cis-stilbene/fluorene hybrids as ambipolar, fluorescent materials for organic light emitting diode applications
RSC Advances, 2013, 3, 9381
7239077 CIFC58 H39 N3P -110.7569; 13.6042; 16.642
106.93; 104.183; 90.917
2248.77Chen, Chien-Tien; Chao, Wei-Shan; Liu, Hao-Wei; Wei, Yi; Jou, Jwo-Huei; Kumar, Sudhir
Spirally configured cis-stilbene/fluorene hybrids as ambipolar, fluorescent materials for organic light emitting diode applications
RSC Advances, 2013, 3, 9381
7239078 CIFC60 H55 B NP -113.1698; 14.2017; 25.4887
100.776; 96.286; 94.685
4629.48Chen, Chien-Tien; Chao, Wei-Shan; Liu, Hao-Wei; Wei, Yi; Jou, Jwo-Huei; Kumar, Sudhir
Spirally configured cis-stilbene/fluorene hybrids as ambipolar, fluorescent materials for organic light emitting diode applications
RSC Advances, 2013, 3, 9381
7239079 CIFC54 H39 Cl2 NP -110.703; 13.3547; 14.8791
92.18; 90.261; 109.366
2004.6Chen, Chien-Tien; Chao, Wei-Shan; Liu, Hao-Wei; Wei, Yi; Jou, Jwo-Huei; Kumar, Sudhir
Spirally configured cis-stilbene/fluorene hybrids as ambipolar, fluorescent materials for organic light emitting diode applications
RSC Advances, 2013, 3, 9381
7239080 CIFC17 H16 Fe N2 OP n a 2120.791; 5.874; 11.646
90; 90; 90
1422.3Kashyap, Bishwapran; Phukan, Prodeep
A new ferrocene-based bulky pyridine as an efficient reusable homogeneous catalyst
RSC Advances, 2013, 3, 15327
7239081 CIFC24 H22 Fe N4 O2C 1 2/c 128.447; 6.2758; 12.914
90; 116.647; 90
2060.6Kashyap, Bishwapran; Phukan, Prodeep
A new ferrocene-based bulky pyridine as an efficient reusable homogeneous catalyst
RSC Advances, 2013, 3, 15327
7239082 CIFC28 H29 F6 N O3P 21 21 215.9746; 17.1181; 25.5543
90; 90; 90
2613.5Romanski, Jan; Nowak, Piotr; Maksymiuk, Anna; Chapuis, Christian; Jurczak, Janusz
Diastereoselective 1,3-dipolar cycloadditions of both electronically modified phenyl-nitrile oxides and stilbenes
RSC Advances, 2013, 3, 23105
7239083 CIFC32 H47 N O5P 1 21 19.0578; 17.9136; 10.2169
90; 113.597; 90
1519.16Romanski, Jan; Nowak, Piotr; Maksymiuk, Anna; Chapuis, Christian; Jurczak, Janusz
Diastereoselective 1,3-dipolar cycloadditions of both electronically modified phenyl-nitrile oxides and stilbenes
RSC Advances, 2013, 3, 23105
7239084 CIFC26 H20 Br N3 O2 SP 1 21/c 116.705; 21.458; 12.8736
90; 99.698; 90
4548.7Postolachi, Rodica; Danac, Ramona; Buurma, Niklaas J.; Pui, Aurel; Balan, Mihaela; Shova, Sergiu; Deleanu, Calin
New cycloimmonium ylide ligands and their palladium(ii) affinities
RSC Advances, 2013, 3, 17260
7239085 CIFC60 H42 Cl6 N4C 1 2/c 117.4912; 12.3477; 23.7674
90; 93.302; 90
5124.7Tanaka, Kazuki; Aratani, Naoki; Kuzuhara, Daiki; Sakamoto, Sadaaki; Okujima, Tetsuo; Ono, Noboru; Uno, Hidemitsu; Yamada, Hiroko
A soluble bispentacenequinone precursor for creation of directly 6,6′-linked bispentacenes and a tetracyanobipentacenequinodimethane
RSC Advances, 2013, 3, 15310
7239086 CIFC45 H25 Cl3 O2C 1 2/c 124.8385; 11.3087; 12.6953
90; 112.668; 90
3290.54Tanaka, Kazuki; Aratani, Naoki; Kuzuhara, Daiki; Sakamoto, Sadaaki; Okujima, Tetsuo; Ono, Noboru; Uno, Hidemitsu; Yamada, Hiroko
A soluble bispentacenequinone precursor for creation of directly 6,6′-linked bispentacenes and a tetracyanobipentacenequinodimethane
RSC Advances, 2013, 3, 15310
7239087 CIFC45 H25 Cl3 O2P -111.4108; 11.8461; 13.6538
83.843; 66.38; 84.23
1677.9Tanaka, Kazuki; Aratani, Naoki; Kuzuhara, Daiki; Sakamoto, Sadaaki; Okujima, Tetsuo; Ono, Noboru; Uno, Hidemitsu; Yamada, Hiroko
A soluble bispentacenequinone precursor for creation of directly 6,6′-linked bispentacenes and a tetracyanobipentacenequinodimethane
RSC Advances, 2013, 3, 15310
7239088 CIFC52 H40 O2P 1 21/n 110.2853; 12.1795; 14.7576
90; 106.415; 90
1773.33Tanaka, Kazuki; Aratani, Naoki; Kuzuhara, Daiki; Sakamoto, Sadaaki; Okujima, Tetsuo; Ono, Noboru; Uno, Hidemitsu; Yamada, Hiroko
A soluble bispentacenequinone precursor for creation of directly 6,6′-linked bispentacenes and a tetracyanobipentacenequinodimethane
RSC Advances, 2013, 3, 15310
7239089 CIFC67 H53 Cl9P 1 21/c 124.018; 10.21; 22.028
90; 90.352; 90
5401.7Tanaka, Kazuki; Aratani, Naoki; Kuzuhara, Daiki; Sakamoto, Sadaaki; Okujima, Tetsuo; Ono, Noboru; Uno, Hidemitsu; Yamada, Hiroko
A soluble bispentacenequinone precursor for creation of directly 6,6′-linked bispentacenes and a tetracyanobipentacenequinodimethane
RSC Advances, 2013, 3, 15310

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