Crystallography Open Database

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Searching year of publication is 2015

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1531044 CIFC30 H22 O4P 1 21 17.0717; 8.8439; 19.5443
90; 96.556; 90
1214.33Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531045 CIFC38.5 H29 Cl O4C 1 2 116.8074; 10.9989; 16.649
90; 92.018; 90
3075.9Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531046 CIFC27 H23 N O4P 1 21 18.1626; 12.2302; 11.0742
90; 101.402; 90
1083.72Wang, De; Wang, Guo-Peng; Sun, Yao-Liang; Zhu, Shou-Fei; Wei, Yin; Zhou, Qi-Lin; Shi, Min
Chiral phosphine-catalyzed tunable cycloaddition reactions of allenoates with benzofuranone-derived olefins for a highly regio-, diastereo- and enantioselective synthesis of spiro-benzofuranones
Chem. Sci., 2015, 6, 7319
1531047 CIFC30 H21 F3 N2C 1 2/c 128.3793; 8.2635; 21.2253
90; 112.455; 90
4600.2Mukundam, Vanga; Kumar, Atul; Dhanunjayarao, Kunchala; Ravi, Arthi; Peruncheralathan, S.; Venkatasubbaiah, Krishnan
Tetraaryl pyrazole polymers: versatile synthesis, aggregation induced emission enhancement and detection of explosives
Polym. Chem., 2015, 6, 7764
1531166 CIFC28 H26 N2 O4 S2P -19.2332; 11.8033; 13.4383
78.564; 74.091; 80.538
1371.04Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui
Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.
Organic letters, 2015, 17, 4870-4873
1531170 CIFC28 H26 N2 O4 S2P 21 21 217.8395; 12.02537; 26.9644
90; 90; 90
2542.01Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui
Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.
Organic letters, 2015, 17, 4870-4873
1531174 CIFC28 H26 N2 O4 S2P 21 21 215.35547; 17.35361; 27.184
90; 90; 90
2526.39Hou, Wenduan; Wei, Qi; Liu, Guisheng; Chen, Jing; Guo, Jing; Peng, Yungui
Asymmetric Multicomponent Sulfa-Michael/Mannich Cascade Reaction: Synthetic Access to 1,2-Diamino-3-Organosulfur Compounds and 2-Nitro Allylic Amines.
Organic letters, 2015, 17, 4870-4873
1531311 CIFC60 H79 B N3 O2 Sc SiP -112.489; 12.502; 20.618
84.375; 75.312; 65.747
2839.1Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531312 CIFC54 H81 B N3 O2 Sc SiP 1 21/n 113.706; 12.501; 31.255
90; 97.34; 90
5311Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531313 CIFC53 H75 B N3 O4 Sc SiP -112.0903; 12.7458; 18.106
93.545; 99.571; 114.287
2481.3Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531314 CIFC59 H79 B N4 O Sc SiP -112.7148; 14.2837; 15.4973
102.293; 99.228; 91.066
2710.3Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531315 CIFC50 H71 B N3 O2 Sc SiP 1 21/c 112.8438; 20.755; 18.74
90; 108.462; 90
4738.5Wang, Baoli; Kang, Xiaohui; Nishiura, Masayoshi; Luo, Yi; Hou, Zhaomin
Isolation, structure and reactivity of a scandium boryl oxycarbene complex
Chem. Sci., 2015
1531316 CIFC24 H17 N OP 1 21/n 112.9997; 21.3361; 13.502
90; 106.398; 90
3592.6Poudel, Tej Narayan; Lee, Yong Rok
Construction of highly functionalized carbazoles via condensation of an enolate to a nitro group
Chem. Sci., 2015, 6, 7028
1531795 CIFC22 H26 O9P 1 21 16.58475; 12.3394; 13.1873
90; 101.317; 90
1050.66Wang, Yuezhou; Qi, Shuang; Zhan, Ying; Zhang, Nanwen; Wu, An-An; Gui, Fu; Guo, Kai; Yang, Yanru; Cao, Shugeng; Hu, Zhiyu; Zheng, Zhonghui; Song, Siyang; Xu, Qingyan; Shen, Yuemao; Deng, Xianming
Aspertetranones A-D, Putative Meroterpenoids from the Marine Algal-Associated Fungus Aspergillus sp. ZL0-1b14.
Journal of natural products, 2015, 78, 2405-2410
1531937 CIFC98 H96 B F24 N2 O Pd TlP -112.7422; 26.6786; 28.5026
99.098; 90.144; 90.509
9566.9Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531938 CIFC108 H102 B F24 N2 Pd TlP -112.5519; 20.2591; 21.647
105.597; 102.325; 97.308
5079.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531939 CIFC152 H172 Ag4 F12 N4 O12 Pt2 S4P 1 21/n 111.7798; 29.62; 20.9358
90; 90.39; 90
7304.7Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531940 CIFC81 H92 Ag F3 N2 O3 Pt SP 1 21/n 118.6061; 19.7722; 20.9507
90; 106.515; 90
7389.5Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531941 CIFC71 H94 F3 N2 O5 Pt S TlP -113.95; 16.2777; 17.6213
66.887; 70.018; 71.465
3379.6Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531942 CIFC93 H134 Ag F3 N2 O10.5 Pd SP 21 21 2115.5936; 21.315; 24.141
90; 90; 90
8023.9Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531943 CIFC79 H106 Ag F3 N5 O4 Pt SP 21 21 2115.6478; 21.2503; 24.077
90; 90; 90
8006.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531944 CIFC84 H98 Ag F3 N2 O3 Pd SP -114.5289; 15.663; 17.673
96.662; 109.412; 94.019
3742.1Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531945 CIFC98 H96 B F24 N2 O Pt TlP -112.7326; 26.642; 28.428
99.2; 90.224; 90.514
9518.8Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531946 CIFC94 H86 B F24 N2 Pt TlP -114.6265; 20.6542; 31.1986
76.597; 79.378; 89.566
9005.2Barnett, Brandon R.; Moore, Curtis E.; Chandrasekaran, Perumalreddy; Sproules, Stephen; Rheingold, Arnold L.; DeBeer, Serena; Figueroa, Joshua S.
Metal-only Lewis pairs between group 10 metals and Tl(i) or Ag(i): insights into the electronic consequences of Z-type ligand binding
Chem. Sci., 2015, 6, 7169
1531947 CIFC3 H7 Cl3 I0 N O0 PbP 43 21 210.4482; 10.4482; 14.7573
90; 90; 90
1611Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong
Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission
Chem. Sci., 2015, 6, 7222
1531948 CIFC80 H180 Cl59 N16 O2 Pb21P 1 21/c 121.2016; 15.9211; 26.4092
90; 91.811; 90
8910Wang, Guan-E; Xu, Gang; Wang, Ming-Sheng; Cai, Li-Zhen; Li, Wen-Hua; Guo, Guo-Cong
Semiconductive 3-D haloplumbate framework hybrids with high color rendering index white-light emission
Chem. Sci., 2015, 6, 7222
1532146 CIFC24 H12 N6 O6P b c n7.235; 41.244; 21.816
90; 90; 90
6510Zhan, Tian-Guang; Zhou, Tian-You; Qi, Qiao-Yan; Wu, Jian; Li, Guang-Yu; Zhao, Xin
The construction of supramolecular polymers through anion bridging: from frustrated hydrogen-bonding networks to well-ordered linear arrays
Polym. Chem., 2015, 6, 7586
1532452 CIFC15 H34 I2 N4 Ni O4 S2P -110.141; 11.619; 11.643
86.263; 69.71; 76.551
1251.3Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532453 CIFC15 H29 Co N2 O6 S2P -17.5419; 8.0477; 16.687
78.174; 82.069; 86.421
981.2Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532454 CIFC15 H28 Fe N2 O6 S2P -17.486; 8.04; 16.74
78.165; 82.235; 86.603
976.6Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532455 CIFC30 H56 Cu2 N4 O12 S4C 1 2/c 119.683; 12.1661; 19.517
90; 106.346; 90
4484.7Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532456 CIFC11 H24 N2 O2 S2P 1 21/c 19.6252; 12.3461; 12.2335
90; 103.606; 90
1413Denny, J. A.; Foley, W. S.; Todd, A. D.; Darensbourg, M. Y.
The ligand unwrapping/rewrapping pathway that exchanges metals in S-acetylated, hexacoordinate N2S2O2complexes
Chem. Sci., 2015, 6, 7079
1532457 CIFC32 H40 S3P -19.799; 11.932; 13.735
84.22; 72.85; 66.98
1412.1Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532458 CIFC32 H40 S3P -110.274; 10.828; 13.62
73.61; 83.52; 85.57
1443Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532459 CIFC28 H32 S3P -17.769; 12.591; 12.753
93.524; 98.169; 101.228
1206.1Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532460 CIFC24 H24 S3P 1 21/c 111.959; 22.114; 7.632
90; 97.436; 90
2001Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532461 CIFC16 H8 S3P 1 21/c 113.033; 3.916; 24.464
90; 103.214; 90
1215.5Mitsudo, Koichi; Sato, Hidehiko; Yamasaki, Arata; Kamimoto, Natsuyo; Goto, Jun; Mandai, Hiroki; Suga, Seiji
Synthesis and Properties of Ethene-Bridged Terthiophenes.
Organic letters, 2015, 17, 4858-4861
1532465 CIFC47.5 H62.5 F6 N1.5 O6.5 PP 1 2/c 115.9874; 18.0758; 18.1871
90; 107.85; 90
5002.8Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei
Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities
Chem. Sci., 2015, 6, 6731
1532466 CIFC138 H129 F18 N3 O18 P3R -3 :H43.2165; 43.2165; 12.4664
90; 90; 120
20163.7Jia, Fei; He, Zhenfeng; Yang, Liu-Pan; Pan, Zhi-Sheng; Yi, Min; Jiang, Ren-Wang; Jiang, Wei
Oxatub[4]arene: a smart macrocyclic receptor with multiple interconvertible cavities
Chem. Sci., 2015, 6, 6731
1532468 CIFC82 H116 Cd2 N24 O25C 1 2/c 130.664; 17.225; 27.371
90; 105.9; 90
13904Sun, Chun-Yi; To, Wai-Pong; Wang, Xin-Long; Chan, Kaai-Tung; Su, Zhong-Min; Che, Chi-Ming
Metal‒organic framework composites with luminescent gold(iii) complexes. Strongly emissive and long-lived excited states in open air and photo-catalysis
Chem. Sci., 2015, 6, 7105
1532469 CIFC91.5 H111.5 Ge2 N2 Si2P -110.806; 18.897; 21.557
108.61; 90.43; 103.93
4032.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532470 CIFC104 H122 Ge2 N2 O2 Si2P 1 21/n 113.373; 21.643; 15.884
90; 102.62; 90
4486.3Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532471 CIFC46 H57 Ge N SiP -110.783; 11.465; 16.298
97.01; 91.76; 92.77
1996.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532472 CIFC52 H61 Ge N SiP 1 21/n 111.543; 23.7164; 16.3022
90; 97.979; 90
4419.7Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532473 CIFC49 H61 Ge N SiP 1 21/c 110.319; 18.286; 22.437
90; 91.27; 90
4232.7Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532474 CIFC50 H63 Ge N SiP 1 21 110.2741; 14.6818; 14.6417
90; 102.077; 90
2159.71Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532475 CIFC52 H67 Ge N SiP 1 21/n 19.942; 15.413; 28.793
90; 97.18; 90
4377.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532476 CIFC46 H57 N Si SnP -110.673; 12.534; 15.493
82.27; 85.09; 73.63
1968Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532477 CIFC52 H68 N Si SnP -110.2591; 13.6505; 17.3164
99.111; 105.293; 95.189
2287.3Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532478 CIFC53 H61 Ge N SiP 1 21/n 110.0813; 15.796; 28.096
90; 96.916; 90
4441.6Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532479 CIFC53 H61 N Si SnP 1 21/n 110.1088; 15.7379; 28.106
90; 96.853; 90
4439.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532480 CIFC52 H65 Ge N SiP 1 21/n 110.003; 15.4017; 28.92
90; 97.698; 90
4415.4Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532481 CIFC49 H63 Ge N SiP 1 21/n 111.374; 23.3065; 16.3439
90; 97.891; 90
4291.5Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532482 CIFC49 H62 Cl Ge N SiP -110.731; 14.446; 15.647
77.83; 78.54; 69.06
2194.2Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532483 CIFC48 H63 Ge N O SiP -110.399; 14.2109; 15.4524
90.483; 101.026; 105.118
2159.72Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532484 CIFC53 H70 N2 O Si SnP -114.604; 15.84; 20.773
88.61; 82.84; 84.99
4749.2Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532485 CIFC112 H154 Ge2 N2 O2 Si2P 1 21/n 115.0392; 12.4994; 26.2128
90; 93.127; 90
4920.17Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532486 CIFC112 H158 N2 O2 Si2 Sn2P -115.4827; 16.4448; 23.7823
72.311; 88.259; 62.908
5094.1Hadlington, Terrance J.; Hermann, Markus; Frenking, Gernot; Jones, Cameron
Two-coordinate group 14 element(ii) hydrides as reagents for the facile, and sometimes reversible, hydrogermylation/hydrostannylation of unactivated alkenes and alkynes
Chem. Sci., 2015, 6, 7249
1532487 CIFC23 H32 O7P 21 21 219.772; 13.5369; 16.5519
90; 90; 90
2189.53Ma, Guoxu; Wu, Haifeng; Chen, Deli; Zhu, Nailiang; Zhu, Yindi; Sun, Zhonghao; Li, Pengfei; Yang, Junshan; Yuan, Jingquan; Xu, Xudong
Antimalarial and Antiproliferative Cassane Diterpenes of Caesalpinia sappan.
Journal of natural products, 2015, 78, 2364-2371
1532490 CIFC27 H30 B2 D3 N2 O2P -16.2435; 13.8921; 14.2338
100.533; 92.139; 100.164
1191.63Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532491 CIFC30 H34 B2 N2 O2P -112.0335; 13.357; 17.045
73.663; 81.968; 79.686
2575Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532492 CIFC31 H36 B2 N2 O2P 1 21/n 19.498; 9.09; 30.647
90; 94.119; 90
2639.1Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532493 CIFC30 H33 B2 Br N2 O2P 1 21/n 19.5066; 9.248; 30.632
90; 94.399; 90
2685.1Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532494 CIFC32 H39 B2 N2 O2P 1 21/n 18.8862; 21.985; 14.0495
90; 96.2349; 90
2728.5Wu, Di; Ganguly, Rakesh; Li, Yongxin; Hoo, Sin Ni; Hirao, Hajime; Kinjo, Rei
Reversible [4 + 2] cycloaddition reaction of 1,3,2,5-diazadiborinine with ethylene
Chem. Sci., 2015, 6, 7150
1532495 CIFC33 H52 I P2 PdP b c a14.978; 16.438; 29.361
90; 90; 90
7229Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532496 CIFC65 H64 B F24 I P2 PdP 1 21/n 114.0602; 28.6171; 16.9031
90; 92.0331; 90
6796.9Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532497 CIFC33 H53 I P2 PdP 1 21/c 112.8203; 14.834; 19.174
90; 106.641; 90
3493.7Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532498 CIFC40 H60 I N P2 PdP 1 21/n 117.0891; 14.014; 18.4206
90; 100.081; 90
4343.4Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532499 CIFC39 H57 I O P2 PdP -111.8764; 14.433; 25.1741
101.297; 93.5784; 111.2
3903Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532500 CIFC68 H72 B F24 I P3 PdP 1 21 110.0901; 23.7955; 31.205
90; 90.532; 90
7492Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532501 CIFC44 H67 F3 O4 P2 Pd S2P 21 21 2114.0266; 15.2323; 21.3735
90; 90; 90
4566.6Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532502 CIFC50 H74 P2 Pd S2P 1 21/n 111.297; 11.59; 36.768
90; 92.926; 90
4808Cui, Peng; Iluc, Vlad M.
Redox-induced umpolung of transition metal carbenes
Chem. Sci., 2015, 6, 7343
1532507 CIFC8 H4 F S3P n m a7.784; 22.5821; 9.6099
90; 90; 90
1689.22Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532508 CIFC16 H10 S6C 1 2/c 124.2039; 6.2548; 22.525
90; 103.733; 90
3312.6Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532509 CIFC12 H6 S6 Se2P b c a16.5074; 8.21747; 23.5969
90; 90; 90
3200.9Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532510 CIFC12 H6 S8P 1 21/c 18.3161; 20.227; 9.2199
90; 92.391; 90
1549.53Debnath, Sashi; Bedi, Anjan; Zade, Sanjio S.
Thienopentathiepine: a sulfur containing fused heterocycle for conjugated systems and their electrochemical polymerization
Polym. Chem., 2015, 6, 7658
1532833 CIFC21 H28 N2 O4P 21 21 218.7278; 9.6635; 46.6791
90; 90; 90
3937Chung, John Y. L.; Marcune, Benjamin; Strotman, Hallena R.; Petrova, Rositza I.; Moore, Jeffrey C.; Dormer, Peter G.
Synthesis of ((3R,6R)-6-Methylpiperidin-3-yl)methanol via Biocatalytic Transamination and Crystallization-Induced Dynamic Resolution
Organic Process Research & Development, 2015, 19, 1418
1533007 CIFC75 H88 Mo4 O8 P2 Sm2P -19.5023; 12.6103; 15.1418
97.784; 90.79; 100.069
1768.68Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533008 CIFC68 H80 Mo4 O8 P2 Yb2P -19.4563; 12.5189; 14.9787
84.903; 71.669; 76.285
1635Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533009 CIFC68 H86 Mo2 O4 P4 Sm2P -19.6185; 10.2667; 17.5096
83.519; 77.307; 78.461
1648.4Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533010 CIFC81 H105 Mo3 O6 P5 Sm3P 1 21/m 110.13; 25.686; 15.724
90; 96.36; 90
4066.2Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533011 CIFC78 H106 Mo2 O4 P6 Sm2P -111.1671; 12.7931; 14.7276
98.952; 110.227; 95.319
1925.7Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533012 CIFC78 H106 Mo2 O4 P6 Yb2P -111.1924; 12.6285; 14.6371
99.581; 110.455; 94.847
1888.44Arleth, Nicholas; Gamer, Michael T.; Köppe, Ralf; Pushkarevsky, Nikolay A.; Konchenko, Sergey N.; Fleischmann, Martin; Bodensteiner, Michael; Scheer, Manfred; Roesky, Peter W.
The approach to 4d/4f-polyphosphides
Chem. Sci., 2015, 6, 7179
1533373 CIFC28 H42 Au Cl3 N4 OI 41/a37.1846; 37.1846; 9.743
90; 90; 90
13471.6Ramsay, William J.; Foster, Jonathan A.; Moore, Katharine L.; Ronson, Tanya K.; Mirgalet, Raphaël J.; Jefferson, David A.; Nitschke, Jonathan R.
AuICl-bound N-heterocyclic carbene ligands form MII4(LAuCl)6integrally gilded cages
Chem. Sci., 2015, 6, 7326
1533374 CIFC30 H33 Cl F3 Ir N2 O2P 1 21/n 111.3662; 17.1523; 15.528
90; 111.111; 90
2824.1Yellol, Jyoti; Pérez, Sergio A; Buceta, Alicia; Yellol, Gorakh; Donaire, Antonio; Szumlas, Piotr; Bednarski, Patrick J.; Makhloufi, Gamall; Janiak, Christoph; Espinosa, Arturo; Ruiz, José
Novel C,N-Cyclometalated Benzimidazole Ruthenium(II) and Iridium(III) Complexes as Antitumor and Antiangiogenic Agents: A Structure-Activity Relationship Study.
Journal of medicinal chemistry, 2015, 58, 7310-7327
1533375 CIFC30 H32 Cl F3 N2 O2 RuP 1 21/c 112.5656; 17.1429; 13.9971
90; 108.785; 90
2854.5Yellol, Jyoti; Pérez, Sergio A; Buceta, Alicia; Yellol, Gorakh; Donaire, Antonio; Szumlas, Piotr; Bednarski, Patrick J.; Makhloufi, Gamall; Janiak, Christoph; Espinosa, Arturo; Ruiz, José
Novel C,N-Cyclometalated Benzimidazole Ruthenium(II) and Iridium(III) Complexes as Antitumor and Antiangiogenic Agents: A Structure-Activity Relationship Study.
Journal of medicinal chemistry, 2015, 58, 7310-7327
1533376 CIFC25.5 H28 O12.5P 21 21 2115.0788; 17.5135; 19.2065
90; 90; 90
5072.1Gan, Maoluo; Liu, Bin; Tan, Yi; Wang, Qiang; Zhou, Hongxia; He, Hongwei; Ping, Yuhui; Yang, Zhaoyong; Wang, Yiguang; Xiao, Chunling
Saccharothrixones A-D, Tetracenomycin-Type Polyketides from the Marine-Derived Actinomycete Saccharothrix sp. 10-10.
Journal of natural products, 2015, 78, 2260-2265
1534094 CIFC79 H60 Cl2 N10 O7 RuP -112.6643; 15.7605; 18.076
105.968; 97.219; 99.105
3370.1Fan, Congbin; Ye, Changqing; Wang, Xiaomei; Chen, Zhigang; Zhou, Yuyang; Liang, Zuoqin; Tao, Xutang
Synthesis and Electrochromic Properties of New Terpyridine‒Triphenylamine Hybrid Polymers
Macromolecules, 2015, 48, 6465
1534095 CIFC32 H40 N0 O8P 21 21 218.2474; 12.543; 29.019
90; 90; 90
3001.9Yang, Shanshan; Sun, Jiachen; Lu, Hong; Ma, Hong; Zhang, Yaozhou
Bioactivity-guided isolation of anticancer compounds from Euphorbia lathyris
Anal. Methods, 2015, 7, 9568
1534096 CIFC16 H16 Br N O2P 21 21 215.1904; 9.7263; 29.581
90; 90; 90
1493.3Pathipati, Stalin R.; Singh, Vipender; Eriksson, Lars; Selander, Nicklas
Lewis Acid Catalyzed Annulation of Nitrones with Oxiranes, Aziridines, and Thiiranes.
Organic letters, 2015, 17, 4506-4509
1534097 CIFC27 H21 N O4P 1 21/c 111.7836; 8.1908; 21.1196
90; 92.216; 90
2036.9Jung, Youngeun; Kim, Ikyon
Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles.
Organic letters, 2015, 17, 4600-4603
1534098 CIFC26 H21 N O3P 1 21/c 111.5406; 9.3427; 18.9135
90; 96.804; 90
2024.9Jung, Youngeun; Kim, Ikyon
Deformylative Intramolecular Hydroarylation: Synthesis of Benzo[e]pyrido[1,2-a]indoles.
Organic letters, 2015, 17, 4600-4603
1534099 CIFC62 H60 Cl N4 O4 PP 1 21 113.9954; 19.389; 14.02
90; 115.309; 90
3439.3Gao, Xing; Han, Jianwei; Wang, Limin
Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles.
Organic letters, 2015, 17, 4596-4599
1534100 CIFC65 H65 N4 O5 PP 1 21 112.0658; 17.7295; 13.2309
90; 104.155; 90
2744.4Gao, Xing; Han, Jianwei; Wang, Limin
Design of Highly Stable Iminophosphoranes as Recyclable Organocatalysts: Application to Asymmetric Chlorinations of Oxindoles.
Organic letters, 2015, 17, 4596-4599
1534101 CIFC24 H29 F N2 O5R 3 :H31.82; 31.82; 6.203
90; 90; 120
5439.2Bonetti, Andrea; Pellegrino, Sara; Das, Priyadip; Yuran, Sivan; Bucci, Raffaella; Ferri, Nicola; Meneghetti, Fiorella; Castellano, Carlo; Reches, Meital; Gelmi, Maria Luisa
Dipeptide Nanotubes Containing Unnatural Fluorine-Substituted β(2,3)-Diarylamino Acid and l-Alanine as Candidates for Biomedical Applications.
Organic letters, 2015, 17, 4468-4471
1534102 CIFC15 H17 N3P 1 21/c 19.507; 9.4923; 14.387
90; 90.344; 90
1298.3Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick
Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton.
Organic letters, 2015, 17, 4518-4521
1534103 CIFC24 H21 NP 1 21/c 17.4677; 18.793; 24.102
90; 94.988; 90
3369.7Hassan, Haitham; Mohammed, Shireen; Robert, Frédéric; Landais, Yannick
Total Synthesis of (±)-Eucophylline. A Free-Radical Approach to the Synthesis of the Azabicyclo[3.3.1]nonane Skeleton.
Organic letters, 2015, 17, 4518-4521
1534104 CIFC13 H14 B Cl F2 N2I 41/a :225.108; 25.108; 8.6289
90; 90; 90
5439.8Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.
Organic letters, 2015, 17, 4632-4635
1534105 CIFC16 H11 B Cl2 F2 N2 OC 1 2/c 115.6318; 13.1816; 15.4701
90; 96.971; 90
3164.1Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.
Organic letters, 2015, 17, 4632-4635
1534106 CIFC12 H11 B Cl2 F2 N2P -110.1284; 11.8356; 12.656
91.216; 110.273; 107.739
1341.8Zhou, Xin; Yu, Changjiang; Feng, Zeya; Yu, Yang; Wang, Jun; Hao, Erhong; Wei, Yun; Mu, Xiaolong; Jiao, Lijuan
Highly Regioselective α-Chlorination of the BODIPY Chromophore with Copper(II) Chloride.
Organic letters, 2015, 17, 4632-4635
1534107 CIFC20 H13 F3 O2 SP -17.4471; 9.4405; 12.781
79.059; 79.842; 75.136
844.95Xu, Chunfa; Shen, Qilong
Lewis Acid Mediated Trifluoromethylthio Lactonization/Lactamization.
Organic letters, 2015, 17, 4561-4563
1534108 CIFC24 H21 N O4 SP 1 21/n 18.2556; 14.406; 17.938
90; 93.63; 90
2129.1Liu, Hongxu; Yang, Yanyan; Wang, Shen; Wu, Jie; Wang, Xiao-Na; Chang, Junbiao
Synthesis of 3-Substituted 2-Aminochromones via Sn(IV)-Promoted Annulation of Ynamides with 2-Methoxyaroyl Chlorides.
Organic letters, 2015, 17, 4472-4475
1534109 CIFC14 H11 N O SP -15.9946; 7.961; 12.7201
85.167; 84.614; 73.532
578.51Lemercier, Bérénice C; Pierce, Joshua G.
Synthesis of 1,4,2-Oxathiazoles via Oxidative Cyclization of Thiohydroximic Acids.
Organic letters, 2015, 17, 4542-4545
1534110 CIFC25 H22 Cl2 I N3 O4 SP 1 21 110.469; 11.122; 11.473
90; 92.129; 90
1335Tripathi, Chandra Bhushan; Mukherjee, Santanu
Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes.
Organic letters, 2015, 17, 4424-4427
1534111 CIFC18 H16 I N OP 1 21 19.9179; 5.7432; 14.186
90; 95.817; 90
803.88Tripathi, Chandra Bhushan; Mukherjee, Santanu
Catalytic Enantioselective 1,4-Iodofunctionalizations of Conjugated Dienes.
Organic letters, 2015, 17, 4424-4427
1534112 CIFC21 H21 N O5 SP 1 21 111.3632; 11.802; 15.831
90; 109.817; 90
1997.3Qiao, Baokun; Huang, Yin-Jun; Nie, Jing; Ma, Jun-An
Highly Regio-, Diastereo-, and Enantioselective Mannich Reaction of Allylic Ketones and Cyclic Ketimines: Access to Chiral Benzosultam.
Organic letters, 2015, 17, 4608-4611
1534113 CIFC19 H18 N2 O2P 1 21/c 111.7071; 15.8544; 9.4636
90; 113.637; 90
1609.2Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping
Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles.
Organic letters, 2015, 17, 4502-4505
1534114 CIFC14 H17 N3 O4P 1 21/c 16.9191; 16.135; 14.3518
90; 104.515; 90
1551.09Shao, Jiaan; Liu, Xingyu; Shu, Ke; Tang, Pai; Luo, Jing; Chen, Wenteng; Yu, Yongping
Tuning the Annulation Reactivity of Vinyl Azides and Carbazates: A Divergent Synthesis of Aza-pyrimidinones and Imidazoles.
Organic letters, 2015, 17, 4502-4505
1534115 CIFC33 H25 N3 O2P 1 21/n 116.9438; 7.2054; 21.3218
90; 95.864; 90
2589.49Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun
Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles.
Organic letters, 2015, 17, 4490-4493
1534116 CIFC27 H20 N4 O4P 1 21/c 17.3218; 32.2827; 11.6678
90; 91.975; 90
2756.25Peng, Jing; Ran, Guang-Yao; Du, Wei; Chen, Ying-Chun
Divergent Cyclization Reactions of Morita-Baylis-Hillman Carbonates of 2-Cyclohexenone and Isatylidene Malononitriles.
Organic letters, 2015, 17, 4490-4493
1534117 CIFC21 H19 F3 N4 O2P 1 21/c 122.1268; 5.3611; 16.7753
90; 101.52; 90
1949.86Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A
Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines.
Organic letters, 2015, 17, 4568-4571
1534118 CIFC20 H18 F3 N3 O2P c a 2116.6564; 5.4719; 39.3699
90; 90; 90
3588.3Chung, Tim S.; Lopez, Steven A.; Houk, K. N.; Garcia-Garibay, Miguel A
Stereospecific Synthesis of Substituted Aziridines by a Crystal-to-Crystal Photodenitrogenation of Δ(2)-1,2,3-Triazolines.
Organic letters, 2015, 17, 4568-4571
1534119 CIFC53 H45 N2 O8P 21 21 2111.4428; 15.4354; 24.3994
90; 90; 90
4309.5Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534120 CIFC48 H52 N4 O9P 21 21 214.958; 25.526; 11.093
90; 90; 90
4235.5Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534121 CIFC45 H42 I2 N4 O8C 1 2/c 135.02; 16.0741; 20.002
90; 111.769; 90
10456Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534122 CIFC59 H63 N6 O8C 1 2/c 120.0623; 15.4284; 19.2848
90; 120.843; 90
5125Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534123 CIFC47 H48 N4 O8P 1 21/c 113.787; 14.6; 24.867
90; 105.219; 90
4829.9Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534124 CIFC49 H50 Cl6 N4 O8P -113.203; 13.977; 14.658
90.494; 100.476; 113.249
2434.2Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534125 CIFC45 H44 N4 O8P -112.2439; 13.8398; 14.5323
91.544; 97.532; 110.103
2285.7Bharitkar, Yogesh P.; Das, Mohua; Kumari, Neha; Kumari, M. Padma; Hazra, Abhijit; Bhayye, Sagar S.; Natarajan, Ramalingam; Shah, Siddharth; Chatterjee, Sourav; Mondal, Nirup B.
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection.
Organic letters, 2015, 17, 4440-4443
1534135 CIFC40 H59 Cl2 N2 P RuP 1 21/n 112.2117; 18.0562; 18.2926
90; 103.741; 90
3918Lummiss, Justin A. M.; Higman, Carolyn S.; Fyson, Devon L.; McDonald, Robert; Fogg, Deryn E.
The divergent effects of strong NHC donation in catalysis
Chem. Sci., 2015, 6, 6739
1534136 CIFC39 H35 N OP 1 21/c 119.39657; 15.07422; 10.4257
90; 98.9955; 90
3010.86Deng, Haiqin; He, Zikai; Lam, Jacky W. Y.; Tang, Ben Zhong
Regio- and stereoselective construction of stimuli-responsive macromolecules by a sequential coupling-hydroamination polymerization route
Polym. Chem., 2015, 6, 8297
1534348 CIFC20 H32 O3C 1 2 133.5582; 7.4109; 14.7554
90; 97.8284; 90
3635.4Du, Kun; De Mieri, Maria; Neuburger, Markus; Zietsman, Pieter C.; Marston, Andrew; van Vuuren, Sandy F.; Ferreira, Daneel; Hamburger, Matthias; van der Westhuizen, Jan H.
Labdane and Clerodane Diterpenoids from Colophospermum mopane.
Journal of natural products, 2015, 78, 2494-2504
1534351 CIFC16 H30 N2 O5 SP 6511.4458; 11.4458; 27.7551
90; 90; 120
3148.95Mazzier, Daniela; Carraro, Francesco; Crisma, Marco; Rancan, Marzio; Toniolo, Claudio; Moretto, Alessandro
A terminally protected dipeptide: from crystal structure and self-assembly, through co-assembly with carbon-based materials, to a ternary catalyst for reduction chemistry in water.
Soft matter, 2015, 12, 238-245
1534352 CIFC16 H30 N2 O5 SP 21 21 215.08911; 12.09583; 32.4406
90; 90; 90
1996.95Mazzier, Daniela; Carraro, Francesco; Crisma, Marco; Rancan, Marzio; Toniolo, Claudio; Moretto, Alessandro
A terminally protected dipeptide: from crystal structure and self-assembly, through co-assembly with carbon-based materials, to a ternary catalyst for reduction chemistry in water.
Soft matter, 2015, 12, 238-245
1534401 CIFC38 H57 Cl F19 N7 O5 P3 RuP -110.036; 14.855; 18.895
73.62; 76.36; 87.09
2626Du, Jun; Zhang, Erlong; Zhao, Yao; Zheng, Wei; Zhang, Yang; Lin, Yu; Wang, Zhaoying; Luo, Qun; Wu, Kui; Wang, Fuyi
Discovery of a dual-targeting organometallic ruthenium complex with high activity inducing early stage apoptosis of cancer cells.
Metallomics : integrated biometal science, 2015, 7, 1573-1583
1538419 CIFC24.5 H27 Br2 Cl O6P 21 21 219.7566; 19.1985; 27.6028
90; 90; 90
5170.34Hans, Marcus; Charpentier, Maël; Huch, Volker; Jauch, Johann; Bruhn, Torsten; Bringmann, Gerhard; Quandt, Dietmar
Stereoisomeric Composition of Natural Myrtucommulone A.
Journal of natural products, 2015, 78, 2381-2389
1538420 CIFC48 H55 F3 O10P 1 21 16.4479; 40.961; 17.888
90; 91.687; 90
4722.4Hans, Marcus; Charpentier, Maël; Huch, Volker; Jauch, Johann; Bruhn, Torsten; Bringmann, Gerhard; Quandt, Dietmar
Stereoisomeric Composition of Natural Myrtucommulone A.
Journal of natural products, 2015, 78, 2381-2389
1539135 CIFC20 H15 Cl N2 O3P 1 21/n 116.571; 5.5448; 20.45
90; 111.604; 90
1747Li, Danyang; Yu, Ming; Zhang, Jitan; Liu, Zhanxiang; Zhang, Yuhong
Synthesis of Benzyl Esters via Functionalization of Multiple C-H Bonds by Palladium Catalysis.
Organic letters, 2015, 17, 5300-5303
1540018 CIFC24 H20 Dy2 N2 O17C 1 2/c 118.3085; 9.0788; 19.6464
90; 97.068; 90
3240.8Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng
Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet.
Inorganic chemistry, 2015, 54, 10224-10231
1540019 CIFC26 H28 Dy2 N2 O19C 1 2/c 118.465; 9.2442; 19.699
90; 102.18; 90
3286.8Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng
Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet.
Inorganic chemistry, 2015, 54, 10224-10231
1540020 CIFC24 H20 Dy2 N2 O17P n m a8.6326; 28.1206; 15.3462
90; 90; 90
3725.3Liu, Ke; Li, Huanhuan; Zhang, Xuejing; Shi, Wei; Cheng, Peng
Constraining and Tuning the Coordination Geometry of a Lanthanide Ion in Metal-Organic Frameworks: Approach toward a Single-Molecule Magnet.
Inorganic chemistry, 2015, 54, 10224-10231
1540021 CIFC10 H12 B F4 N O2 RuP 1 21/n 18.7303; 9.7841; 15.4342
90; 91.525; 90
1317.89Nyawade, Eunice A.; Friedrich, Holger B.; Omondi, Bernard; Mpungose, Philani
Synthesis and Characterization of New (η5-Cyclopentadienyl)dicarbonylruthenium(II) Amine Complexes: Their Application as Homogeneous Catalysts in Styrene Oxidation
Organometallics, 2015, 34, 4922
1540022 CIFC14 H14 B F4 N O2 RuP 1 21/n 110.4488; 9.7788; 31.7901
90; 99.236; 90
3206.1Nyawade, Eunice A.; Friedrich, Holger B.; Omondi, Bernard; Mpungose, Philani
Synthesis and Characterization of New (η5-Cyclopentadienyl)dicarbonylruthenium(II) Amine Complexes: Their Application as Homogeneous Catalysts in Styrene Oxidation
Organometallics, 2015, 34, 4922
1540024 CIFC42 H49 Cl2 Eu N12 O16 ZnP -113.8641; 14.5627; 15.19
96.519; 113.081; 109.85
2543.6Anastasiadis, Nikolaos C.; Polyzou, Christina D.; Kostakis, George E.; Bekiari, Vlasoula; Lan, Yanhua; Perlepes, Spyros P.; Konidaris, Konstantis F.; Powell, Annie K.
Dinuclear lanthanide(iii)/zinc(ii) complexes with methyl 2-pyridyl ketone oxime.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19791-19795
1540025 CIFC28 H29 Dy N10 O10 ZnC 1 c 115.9387; 9.3158; 22.5168
90; 94.59; 90
3332.6Anastasiadis, Nikolaos C.; Polyzou, Christina D.; Kostakis, George E.; Bekiari, Vlasoula; Lan, Yanhua; Perlepes, Spyros P.; Konidaris, Konstantis F.; Powell, Annie K.
Dinuclear lanthanide(iii)/zinc(ii) complexes with methyl 2-pyridyl ketone oxime.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19791-19795
1540029 CIFC28 H20 Cu O7P 1 21/n 112.3691; 13.9416; 13.8663
90; 100.45; 90
2351.5Jochyms, Quentin; Guillot, Pierre; Mignard, Emmanuel; Vincent, Jean-Marc
A fluorosurfactant and photoreducible Cu(II)-tren click catalyst: surfactant and catalytic properties at liquid/liquid interfaces.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19700-19707
1540030 CIFC46 H58 Dy2 N14 O24P -19.931; 10.841; 14.4817
82.775; 71.167; 74.627
1421.48Kuo, Che-Jung; Holmberg, Rebecca J.; Lin, Po-Heng
Slight synthetic changes eliciting different topologies: synthesis, structure and magnetic properties of novel dinuclear and nonanuclear dysprosium complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19758-19762
1540031 CIFC80 H92 Dy9 N24 O46C 1 2/c 134.8579; 24.5497; 24.2872
90; 120.453; 90
17916.6Kuo, Che-Jung; Holmberg, Rebecca J.; Lin, Po-Heng
Slight synthetic changes eliciting different topologies: synthesis, structure and magnetic properties of novel dinuclear and nonanuclear dysprosium complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19758-19762
1540032 CIFC28.5 H63 Cl2 Cu2 N4 O19 Zn2P -110.9593; 13.8454; 17.4039
109.186; 90.177; 108.009
2355.8Heras Ojea, María José; Wilson, Claire; Coles, Simon J.; Tuna, Floriana; Murrie, Mark
Directed synthesis of {CuZn} and {CuZn} heterometallic complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19275-19281
1540033 CIFC88 H232 Cl8 Cu8 N16 O96 Zn8P 4/n26.5574; 26.5574; 13.1186
90; 90; 90
9252.5Heras Ojea, María José; Wilson, Claire; Coles, Simon J.; Tuna, Floriana; Murrie, Mark
Directed synthesis of {CuZn} and {CuZn} heterometallic complexes.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 19275-19281
1540373 CIFC135 H42 Cl3 O2C 1 2/c 120.4242; 25.5132; 32.3262
90; 105.672; 90
16218.5Abeyratne Kuragama, Peumie L.; Fronczek, Frank R.; Sygula, Andrzej
Bis-corannulene Receptors for Fullerenes Based on Klärner's Tethers: Reaching the Affinity Limits.
Organic letters, 2015, 17, 5292-5295
1540374 CIFC16 H26 N2 O6 SP 21 21 216.2372; 11.1508; 28.596
90; 90; 90
1988.8Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540375 CIFC13 H21 N O6P 21 21 216.282; 9.924; 24.859
90; 90; 90
1549.8Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540376 CIFC16 H27 N O8P 1 21 110.248; 9.553; 11.932
90; 99.477; 90
1152.2Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540377 CIFC17 H28 N2 O6P 1 21 110.375; 17.5559; 10.8576
90; 95.023; 90
1970Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540378 CIFC19 H24 N2 O6 SP 1 21 111.0948; 6.112; 15.1863
90; 92.704; 90
1028.7Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540379 CIFC20 H26 N2 O6P 1 21 19.6081; 10.7346; 20.0544
90; 91.493; 90
2067.7Berini, Christophe; Sebban, Muriel; Oulyadi, Hassan; Sanselme, Morgane; Levacher, Vincent; Brière, Jean-François
Organocatalyzed Multicomponent Synthesis of Isoxazolidin-5-ones.
Organic letters, 2015, 17, 5408-5411
1540380 CIFC84 H153 Ag3 Au15 O2 S14C 1 2/c 124.9951; 18.5586; 51.826
90; 90.478; 90
24040Xiang, Ji; Li, Peng; Song, Yongbo; Liu, Xia; Chong, Hanbao; Jin, Shan; Pei, Yong; Yuan, Xiaoyou; Zhu, Manzhou
X-Ray crystal structure, and optical and electrochemical properties of the Au15Ag3(SC6H11)14 nanocluster with a core-shell structure.
Nanoscale, 2015, 7, 18278-18283
1540381 CIFC21 H24 Cl Co N7 NiP 1 21/n 114.4536; 9.9877; 14.7366
90; 101.065; 90
2087.8Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540382 CIFC41 H64 Fe N4 O0.5 P3 TiP -112.35; 19.4587; 19.7453
113.034; 95.547; 101.183
4204.9Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540383 CIFC43 H68 N4 Ni O P3 TiP -112.5471; 14.0969; 24.6228
91.787; 98.742; 94.687
4286Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540384 CIFC69 H91 B Co Cr N5 O P3P 1 21/c 117.8979; 14.3708; 26.8674
90; 99.446; 90
6816.8Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540385 CIFC39 H60 B Cr F4 N4 Ni P3R -3 :H12.4121; 12.4121; 57.067
90; 90; 120
7613.9Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540386 CIFC21 H24 Cl Co N7 NiP 1 21/n 114.4978; 10.0084; 14.7758
90; 100.944; 90
2105Eisenhart, Reed J.; Clouston, Laura J.; Lu, Connie C.
Configuring Bonds between First-Row Transition Metals.
Accounts of chemical research, 2015, 48, 2885-2894
1540387 CIFC78 H196 Cu6 Li4 Mn4 N12 O104P 4/m m m36.71; 36.71; 15.414
90; 90; 90
20772Grancha, Thais; Acosta, Alvaro; Cano, Joan; Ferrando-Soria, Jesús; Seoane, Beatriz; Gascon, Jorge; Pasán, Jorge; Armentano, Donatella; Pardo, Emilio
Cation Exchange in Dynamic 3D Porous Magnets: Improvement of the Physical Properties.
Inorganic chemistry, 2015, 54, 10834-10840
1540388 CIFC78 H198 Cu6 K4 Mn4 N12 O105P 4/m m m37.492; 37.492; 15.557
90; 90; 90
21868Grancha, Thais; Acosta, Alvaro; Cano, Joan; Ferrando-Soria, Jesús; Seoane, Beatriz; Gascon, Jorge; Pasán, Jorge; Armentano, Donatella; Pardo, Emilio
Cation Exchange in Dynamic 3D Porous Magnets: Improvement of the Physical Properties.
Inorganic chemistry, 2015, 54, 10834-10840
1540389 CIFC19 H24 F2 N3 Na O7 SP 1 21/c 115.929; 10.828; 13.718
90; 91.62; 90
2365.1Jiang, Chen; Wang, Yongli; Yan, Jiaqi; Yang, Jingxiang; Xiao, Liping; Hao, Hongxun
Formation Mechanism and Phase Transformation Behaviors of Pantoprazole Sodium Heterosolvate
Organic Process Research & Development, 2015, 19, 1752
1540392 CIFBa0.1 O4 Si Sr1.9P m n b5.674; 7.086; 9.745
90; 90; 90
391.81Li, Xiaojun; Hua, Youjie; Ma, Hongping; Deng, Degang; Xu, Shiqing
Modification of the crystal structure of Sr2−xBaxSi(O,N)4: Eu2+phosphors to improve their luminescence properties
CrystEngComm, 2015, 17, 9123
1540393 CIFBa0.15 N O4 Si Sr2.85P m n b5.6796; 7.1386; 9.7639
90; 90; 90
395.87Li, Xiaojun; Hua, Youjie; Ma, Hongping; Deng, Degang; Xu, Shiqing
Modification of the crystal structure of Sr2−xBaxSi(O,N)4: Eu2+phosphors to improve their luminescence properties
CrystEngComm, 2015, 17, 9123
1540394 CIFC17 H16 B Mo N6 O2 P3P -18.7379; 9.957; 13.2391
104.609; 96.252; 107.11
1044.19Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540395 CIFC38 H38 B2 Fe N12 P6P -110.981; 13.5289; 15.9001
91.94; 99.962; 111.752
2148.4Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540396 CIFC34.5 H34 B2 Cd N12 P6P -114.048; 14.097; 14.1551
66.977; 61.712; 61.256
2115.4Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540397 CIFC38 H38 B2 Co N12 P6P -111.132; 13.749; 15.6951
90.726; 99.272; 112.266
2186.9Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540398 CIFC38 H38 B2 N12 Ni P6P -111.091; 13.6971; 15.735
90.977; 99.368; 112.091
2177.3Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540399 CIFC32 H30 B3 Cl6 Co F4 N12 P6C 1 2/c 111.2374; 17.1902; 24.3814
90; 97.463; 90
4669.9Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540400 CIFC12 H11 B N6 P3 TlP n m a9.144; 10.3091; 17.5949
90; 90; 90
1658.61Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540401 CIFC12 H11 B Cl3 N6 P3 TiP 1 21/m 18.281; 10.292; 11.4621
90; 102.607; 90
953.34Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540402 CIFC15 H11 B Mn N6 O3 P3P 1 21/c 116.962; 10.482; 24.6311
90; 112.579; 90
4043.6Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540403 CIFC21 H23 B N7 P3 PdP 1 21/c 19.404; 15.931; 16.528
90; 100.27; 90
2436.5Mlateček, Martin; Dostál, Libor; Růžičková, Zdeňka; Honzíček, Jan; Holubová, Jana; Erben, Milan
The first scorpionate ligand based on diazaphosphole.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20242-20253
1540404 CIFC22 H16 Cu N14 OP -112.3344; 14.2954; 15.4511
95.631; 107.583; 108.242
2410.1Saha, Manideepa; Das, Mriganka; Nasani, Rajendar; Choudhuri, Indrani; Yousufuddin, Muhammed; Nayek, Hari Pada; Shaikh, Mobin M.; Pathak, Biswarup; Mukhopadhyay, Suman
Targeted water soluble copper-tetrazolate complexes: interactions with biomolecules and catecholase like activities.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20154-20167
1540405 CIFC29 H23 Cu N12 O3.5P -111.9248; 11.9276; 13.4576
71.6; 68.381; 70.668
1637.7Saha, Manideepa; Das, Mriganka; Nasani, Rajendar; Choudhuri, Indrani; Yousufuddin, Muhammed; Nayek, Hari Pada; Shaikh, Mobin M.; Pathak, Biswarup; Mukhopadhyay, Suman
Targeted water soluble copper-tetrazolate complexes: interactions with biomolecules and catecholase like activities.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20154-20167
1540406 CIFC24.65 H18 Cr Gd N8 Ni O10.65P 1 21/c 113.071; 12.139; 21.735
90; 106.84; 90
3300.8Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540407 CIFC24.63 H20.52 Cr N8 Ni O10.63 TbP 1 21/c 113.051; 12.15; 21.711
90; 106.89; 90
3294.2Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540408 CIFC25 H18 Fe N8 Ni O11 TbP 1 21/c 112.861; 12.014; 21.577
90; 106.73; 90
3192.8Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540409 CIFC24 H18 Fe Gd N8 Ni O11P 1 21/c 112.862; 12.012; 21.58
90; 106.72; 90
3193.1Chen, Chao; Liu, Yashu; Li, Ping; Zhou, Hongbo; Shen, Xiaoping
Construction of Ni(II)Ln(III)M(III) (Ln = Gd(III), Tb(III); M = Fe(III), Cr(III)) clusters showing slow magnetic relaxations.
Dalton transactions (Cambridge, England : 2003), 2015, 44, 20193-20199
1540410 CIFC142 H120 Gd7 N11 O24P -115.5132; 20.762; 24.831
106.288; 103.085; 105.827
6977.1Mazarakioti, Eleni C.; Cunha-Silva, Luís; Bekiari, Vlasoula; Escuer, Albert; Stamatatos, Theocharis C.
New structural topologies in 4f-metal cluster chemistry from vertex-sharing butterfly units: {LnIII7} complexes exhibiting slow magnetization relaxation and ligand-centred emissions
RSC Advances, 2015, 5, 92534-92538
1540411 CIFC23 H20 N2 OP -19.7936; 10.0349; 10.3079
110.403; 101.163; 102.888
883.8Dandia, Anshu; Sharma, Amit; Parewa, Vijay; Kumawat, Begraj; Rathore, Kuldeep S.; Sharma, Amit
Amidic C–N bond cleavage of isatin: chemoselective synthesis of pyrrolo[2,3,4- <i>kl</i> ]acridin-1-ones using Ag NPs decorated rGO composite as an efficient and recoverable catalyst under microwave irradiation
RSC Advances, 2015, 5, 91888-91902
1540412 CIFC29 H24 N2 O2 SeP 21 21 218.7794; 14.6701; 37.5122
90; 90; 90
4831.4Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540413 CIFC31 H28 N2 O3 SeP 1 21 18.6504; 9.7776; 16.3783
90; 98.688; 90
1369.38Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540414 CIFC22 H23 Br N2 O2 S SeP 1 21 111.244; 7.6728; 12.837
90; 98.983; 90
1093.9Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540415 CIFC16 H15 N SeP 1 21/n 114.8679; 10.004; 18.5854
90; 98.871; 90
2731.3Chang, Wong-Jin; Kulkarni, Manohar V.; Sun, Chung-Ming
Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
RSC Advances, 2015, 5, 97113-97120
1540425 CIFC18 H14 N O4C 2 2 216.8797; 17.32; 26.023
90; 90; 90
3100.8Artuso, Emma; Ghibaudi, Elena; Lace, Beatrice; Marabello, Domenica; Vinciguerra, Daniele; Lombardi, Chiara; Koltai, Hinanit; Kapulnik, Yoram; Novero, Mara; Occhiato, Ernesto G.; Scarpi, Dina; Parisotto, Stefano; Deagostino, Annamaria; Venturello, Paolo; Mayzlish-Gati, Einav; Bier, Ariel; Prandi, Cristina
Stereochemical Assignment of Strigolactone Analogues Confirms Their Selective Biological Activity.
Journal of natural products, 2015, 78, 2624-2633
1540426 CIFC32 H32 O15P 21 21 217.0833; 13.9608; 31.0735
90; 90; 90
3072.81Wu, Guangwei; Yu, Guihong; Kurtán, Tibor; Mándi, Attila; Peng, Jixing; Mo, Xiaomei; Liu, Ming; Li, Hui; Sun, Xinhua; Li, Jing; Zhu, Tianjiao; Gu, Qianqun; Li, Dehai
Versixanthones A-F, Cytotoxic Xanthone-Chromanone Dimers from the Marine-Derived Fungus Aspergillus versicolor HDN1009.
Journal of natural products, 2015, 78, 2691-2698
1540465 CIFC28 H40 O8P 43 21 210.5228; 10.5228; 52.456
90; 90; 90
5808.4Nguyen, Ha T. T.; Truong, Ngan B.; Doan, Huong T. M.; Litaudon, Marc; Retailleau, Pascal; Do, Thao T.; Nguyen, Hung V.; Chau, Minh V.; Pham, Cuong V.
Cytotoxic Clerodane Diterpenoids from the Leaves of Casearia grewiifolia.
Journal of natural products, 2015, 78, 2726-2730
1540466 CIFC38.5 H52 O10.5P 3118.4501; 18.4501; 9.9236
90; 90; 120
2925.5Nguyen, Ha T. T.; Truong, Ngan B.; Doan, Huong T. M.; Litaudon, Marc; Retailleau, Pascal; Do, Thao T.; Nguyen, Hung V.; Chau, Minh V.; Pham, Cuong V.
Cytotoxic Clerodane Diterpenoids from the Leaves of Casearia grewiifolia.
Journal of natural products, 2015, 78, 2726-2730
1540468 CIFC20 H16 Br N OP 21 21 215.616; 13.1439; 22.937
90; 90; 90
1693.1Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540469 CIFC16 H15 Br NP b c a16.0499; 7.6796; 22.6554
90; 90; 90
2792.4Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540470 CIFC22 H20 Br N OP 1 21/n 19.5118; 19.672; 9.821
90; 91.45; 90
1837.1Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540471 CIFC17 H18 Br NP b c a17.503; 8.0333; 21.133
90; 90; 90
2971.4Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540472 CIFC23 H22 Br N OC 1 2/c 118.368; 9.0221; 23.995
90; 102.82; 90
3877.3Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540473 CIFC18 H20 Br NP b c a16.319; 8.0724; 24.455
90; 90; 90
3221.5Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540474 CIFC24 H24 Br N OP 1 21/n 15.7109; 12.738; 28.186
90; 90.021; 90
2050.4Xue, peng chong; Wang, Panpan; Chen, Peng; Yao, Boqi; Gong, Peng; sun, Jiabao; zhang, Zhenqi; Lu, Ran
Bright persistent luminescence from pure organic molecules through moderate intermolecular heavy atom effect
Chem. Sci., 2015
1540475 CIFC18 H19 N O3P 21 21 216.1323; 7.4365; 33.4178
90; 90; 90
1523.95Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540476 CIFC19 H21 N O3P 1 21 18.719; 5.6224; 17.2361
90; 96.032; 90
840.26Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540477 CIFC18 H21 N O4C 1 2 114.0792; 6.7979; 17.748
90; 95.958; 90
1689.47Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540478 CIFC19 H21 N O3P 21 21 217.3552; 13.6032; 17.2196
90; 90; 90
1722.89Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540479 CIFC18 H19 N O3P 21 21 215.9065; 7.9113; 32.9027
90; 90; 90
1537.48Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540480 CIFC18 H17 N O2P 21 21 216.0722; 8.115; 29.7039
90; 90; 90
1463.69Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540481 CIFC21 H19 N O4P b c a9.4116; 15.8331; 24.7415
90; 90; 90
3686.8Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540482 CIFC19 H21 N O3P 1 21 18.5617; 5.5085; 17.2021
90; 103.015; 90
790.45Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540483 CIFC18 H19 N O3P 1 21 19.9132; 7.0748; 11.5133
90; 104.337; 90
782.32Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540484 CIFC19 H21 N O3P 21 21 217.5426; 12.0156; 17.4134
90; 90; 90
1578.16Shen, De-Yang; Nguyen, Thi Ngan; Wu, Shwu-Jen; Shiao, Young-Ji; Hung, Hsin-Yi; Kuo, Ping-Chung; Kuo, Daih-Huang; Thang, Tran Dinh; Wu, Tian-Shung
γ- and δ-Lactams from the Leaves of Clausena lansium.
Journal of natural products, 2015, 78, 2521-2530
1540490 CIFC20 H32 O3P 21 21 217.6689; 10.2286; 22.608
90; 90; 90
1773.42Du, Kun; De Mieri, Maria; Neuburger, Markus; Zietsman, Pieter C.; Marston, Andrew; van Vuuren, Sandy F.; Ferreira, Daneel; Hamburger, Matthias; van der Westhuizen, Jan H.
Labdane and Clerodane Diterpenoids from Colophospermum mopane.
Journal of natural products, 2015, 78, 2494-2504
1540491 CIFC20 H32 O3P 21 21 2114.0499; 17.2599; 31.2403
90; 90; 90
7575.8Du, Kun; De Mieri, Maria; Neuburger, Markus; Zietsman, Pieter C.; Marston, Andrew; van Vuuren, Sandy F.; Ferreira, Daneel; Hamburger, Matthias; van der Westhuizen, Jan H.
Labdane and Clerodane Diterpenoids from Colophospermum mopane.
Journal of natural products, 2015, 78, 2494-2504
1540501 CIFAs3 Ga Sr3P n m a12.757; 19.268; 6.503
90; 90; 90
1598.4Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen
Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)
Crystals, 2015, 5, 433
1540502 CIFAl As3 Ba3C m c e19.854; 6.8636; 13.2849
90; 90; 90
1810.3Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen
Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)
Crystals, 2015, 5, 433
1540503 CIFAs3 Ba3 GaP n m a13.3589; 19.9788; 6.8008
90; 90; 90
1815.1Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen
Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)
Crystals, 2015, 5, 433
1540504 CIFAl Ba3 P3C m c e19.3572; 6.7433; 12.9707
90; 90; 90
1693.1Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen
Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)
Crystals, 2015, 5, 433
1540505 CIFGa P3 Sr3C m c e18.787; 6.3867; 12.403
90; 90; 90
1488.2Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen
Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)
Crystals, 2015, 5, 433
1540506 CIFAl As3 Sr3C m c e19.149; 6.5652; 12.6871
90; 90; 90
1595Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen
Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)
Crystals, 2015, 5, 433
1540507 CIFC9 H16 O2P 1 21/c 110.6473; 5.2855; 17.0313
90; 106.099; 90
920.87Sonneck, Marcel; Peppel, Tim; Spannenberg, Anke; Wohlrab, Sebastian
Synthesis and Molecular Structures of (E)-non-2-enoic Acid and (E)-dec-2-enoic Acid
Crystals, 2015, 5, 466
1540508 CIFC10 H18 O2P -14.1405; 15.2839; 17.7089
68.3291; 83.385; 85.0779
1033.39Sonneck, Marcel; Peppel, Tim; Spannenberg, Anke; Wohlrab, Sebastian
Synthesis and Molecular Structures of (E)-non-2-enoic Acid and (E)-dec-2-enoic Acid
Crystals, 2015, 5, 466
1540509 CIFC24 H26 Ca N4 O14 S2P 21 21 216.355; 17.478; 5.4549
90; 90; 90
1559.3Tai, Xi-Shi; Wang, Xin
Synthesis and Crystal Structure of a 1D Chained Coordination Polymer Constructed from Ca2+ and 2-[(E)-(2-Furoylhydrazono)methyl]benzenesulfonate
Crystals, 2015, 5, 458
1540510 CIFC56 H92 Cl2 N8 Nd2 O2P -110.049; 11.337; 14.471
82.53; 83.02; 73.74
1563Karmel, Isabell; Batrice, Rami; Eisen, Moris
Catalytic Organic Transformations Mediated by Actinide Complexes
Inorganics, 2015, 3, 392
1540511 CIFC38 H54 Li2 N4 O2P -19.6687; 9.948; 19.611
93.77; 91.33; 90.96
1881.4Karmel, Isabell; Batrice, Rami; Eisen, Moris
Catalytic Organic Transformations Mediated by Actinide Complexes
Inorganics, 2015, 3, 392
1540512 CIFC50 H70 Li2 N4 O2P -19.8768; 10.2082; 11.6883
104.144; 90.248; 104.209
1105.18Karmel, Isabell; Batrice, Rami; Eisen, Moris
Catalytic Organic Transformations Mediated by Actinide Complexes
Inorganics, 2015, 3, 392
1540513 CIFC44 H72 Ce Cl2 Li N4 O2 P2 Si4P 1 21/n 111.117; 36.425; 13.538
90; 96.7; 90
5444.6Karmel, Isabell; Batrice, Rami; Eisen, Moris
Catalytic Organic Transformations Mediated by Actinide Complexes
Inorganics, 2015, 3, 392
1540514 CIFC12 H16 O5P 1 21 19.2138; 7.3606; 16.9811
90; 102.272; 90
1125.33Guo, Wenqiang; Zhang, Zhenzhen; Zhu, Tianjiao; Gu, Qianqun; Li, Dehai
Penicyclones A-E, Antibacterial Polyketides from the Deep-Sea-Derived Fungus Penicillium sp. F23-2.
Journal of natural products, 2015, 78, 2699-2703
1540524 CIFC38 H50 N O14P 21 21 2111.0875; 14.3476; 23.495
90; 90; 90
3737.6Reis, Mariana A.; André, Vânia; Duarte, M. Teresa; Lage, Hermann; Ferreira, Maria-José U
12,17-Cyclojatrophane and Jatrophane Constituents of Euphorbia welwitschii.
Journal of natural products, 2015, 78, 2684-2690
1540525 CIFC40 H53 N O15P 1 21 112.0328; 21.7465; 15.6177
90; 95.277; 90
4069.4Reis, Mariana A.; André, Vânia; Duarte, M. Teresa; Lage, Hermann; Ferreira, Maria-José U
12,17-Cyclojatrophane and Jatrophane Constituents of Euphorbia welwitschii.
Journal of natural products, 2015, 78, 2684-2690
1540526 CIFC17 H24 O5P 21 21 217.2341; 12.0603; 19.2403
90; 90; 90
1678.63Li, Tian-Xiao; Yang, Ming-Hua; Wang, Xiao-Bing; Wang, Ying; Kong, Ling-Yi
Synergistic Antifungal Meroterpenes and Dioxolanone Derivatives from the Endophytic Fungus Guignardia sp.
Journal of natural products, 2015, 78, 2511-2520
1540527 CIFC11 H21 N3 O5P 21 21 215.6679; 13.4355; 18.1813
90; 90; 90
1384.53Zheng, Xiu-Mian; Meng, Fan-Wang; Geng, Fang; Qi, Meng; Luo, Cheng; Yang, Li; Wang, Zheng-Tao
Plantadeprate A, a Tricyclic Monoterpene Zwitterionic Guanidium, and Related Derivatives from the Seeds of Plantago depressa.
Journal of natural products, 2015, 78, 2822-2826
1540528 CIFC21 H34 O3P 1 21 17.132; 27.174; 9.624
90; 90.614; 90
1865.1Xie, Chunfeng; Sun, Lingmei; Liao, Kai; Liu, Sheng; Wang, Meicheng; Xu, Jing; Bartlam, Mark; Guo, Yuanqiang
Bioactive ent-Pimarane and ent-Abietane Diterpenoids from the Whole Plants of Chloranthus henryi.
Journal of natural products, 2015, 78, 2800-2807
1540529 CIFC21 H36 O3P 1 21 16.7178; 17.015; 34.5
90; 90.064; 90
3943.5Xie, Chunfeng; Sun, Lingmei; Liao, Kai; Liu, Sheng; Wang, Meicheng; Xu, Jing; Bartlam, Mark; Guo, Yuanqiang
Bioactive ent-Pimarane and ent-Abietane Diterpenoids from the Whole Plants of Chloranthus henryi.
Journal of natural products, 2015, 78, 2800-2807
1540534 CIFC17 H15 N O2P 1 21/c 112.452; 9.3523; 11.841
90; 98.748; 90
1362.9Zhou, Zhi; Liu, Guixia; Chen, Yan; Lu, Xiyan
Cascade Synthesis of 3-Alkylidene Dihydrobenzofuran Derivatives via Rhodium(III)-Catalyzed Redox-Neutral C-H Functionalization/Cyclization.
Organic letters, 2015, 17, 5874-5877
1540535 CIFC44 H28 Cl4 OP -111.3831; 11.7165; 12.5092
77.777; 83.9; 89.052
1621.27Das, Soumyajit; Wu, Jishan
Toward Singlet-Triplet Bistable Nonalternant Kekulé Hydrocarbons: Azulene-to-Naphthalene Rearrangement.
Organic letters, 2015, 17, 5854-5857
1540536 CIFC15 H21 N3 O5P 1 21 16.359; 22.998; 32.023
90; 90.01; 90
4683Zhang, Xiaofei; Yang, Haodong; Tang, Pingping
Transition-Metal-Free Oxidative Aliphatic C-H Azidation.
Organic letters, 2015, 17, 5828-5831
1540537 CIFC15 H24 N2 O2 SP 1 21/c 110.9076; 6.7702; 21.2437
90; 103.38; 90
1526.19Kröger, Denis; Franz, Max; Schmidtmann, Marc; Martens, Jürgen
Sequential Multicomponent Reactions and a Cu-Mediated Rearrangement: Diastereoselective Synthesis of Tricyclic Ketones.
Organic letters, 2015, 17, 5866-5869
1540549 CIFC202 H191 Cl12 N41 O70 Zn9P -119.431; 22.435; 28.802
81.86; 81.6; 75.35
11945Wood, Christopher; Ronson, Tanya; McConnell, Anna; Roberts, Derrick A.; Nitschke, Jonathan
Dual stimuli-induced formation of a μ-hydroxido bridged [Zn9L5(μ-OH)6]12+half-pipe
Chem. Sci., 2015
1540550 CIFC222 H163 F60 N41 O62 S22 Zn9P 1 21/n 115.8416; 55.356; 33.875
90; 90.229; 90
29706Wood, Christopher; Ronson, Tanya; McConnell, Anna; Roberts, Derrick A.; Nitschke, Jonathan
Dual stimuli-induced formation of a μ-hydroxido bridged [Zn9L5(μ-OH)6]12+half-pipe
Chem. Sci., 2015
1540551 CIFC202 H146 F40 N62 O66 S22 Zn9P 61 2 236.8; 36.8; 35.22
90; 90; 120
41306Wood, Christopher; Ronson, Tanya; McConnell, Anna; Roberts, Derrick A.; Nitschke, Jonathan
Dual stimuli-induced formation of a μ-hydroxido bridged [Zn9L5(μ-OH)6]12+half-pipe
Chem. Sci., 2015
1540552 CIFC198 H149 F48 N39 O64 Re4 S16 Zn9P 1 21/c 138.4811; 22.233; 33.8318
90; 115.636; 90
26095.5Wood, Christopher; Ronson, Tanya; McConnell, Anna; Roberts, Derrick A.; Nitschke, Jonathan
Dual stimuli-induced formation of a μ-hydroxido bridged [Zn9L5(μ-OH)6]12+half-pipe
Chem. Sci., 2015
1540559 CIFC15 H13 NP 21 21 216.8195; 8.3525; 20.053
90; 90; 90
1142.2Kanchupalli, Vinaykumar; Joseph, Desna; Katukojvala, Sreenivas
Pyridazine N-Oxides as Precursors of Metallocarbenes: Rhodium-Catalyzed Transannulation with Pyrroles.
Organic letters, 2015, 17, 5878-5881
1540569 CIFC17 H11 F3 N2 O3P 1 21/c 113.835; 14.066; 7.7299
90; 97.446; 90
1491.6Fugard, Alison J.; Thompson, Bethany K.; Slawin, Alexandra M. Z.; Taylor, James E.; Smith, Andrew D.
Organocatalytic Synthesis of Fused Bicyclic 2,3-Dihydro-1,3,4-oxadiazoles through an Intramolecular Cascade Cyclization.
Organic letters, 2015, 17, 5824-5827
1540570 CIFC36.42 H45.33 N8 O15.23 ZrP 1 21/c 119.6642; 12.5427; 16.2481
90; 91.706; 90
4005.7Deri, Melissa A.; Ponnala, Shashikanth; Kozlowski, Paul; Burton-Pye, Benjamin P; Cicek, Huseyin T.; Hu, Chunhua; Lewis, Jason S.; Francesconi, Lynn C.
p-SCN-Bn-HOPO: A Superior Bifunctional Chelator for (89)Zr ImmunoPET.
Bioconjugate chemistry, 2015, 26, 2579-2591
1540571 CIFC11 H14 N2P n m a8.917; 7.6126; 15.0884
90; 90; 90
1024.22Druzhinin, Sergey I.; Galievsky, Victor A.; Demeter, Attila; Kovalenko, Sergey A.; Senyushkina, Tamara; Dubbaka, Srinivas R.; Knochel, Paul; Mayer, Peter; Grosse, Christian; Stalke, Dietmar; Zachariasse, Klaas A.
Two-State Intramolecular Charge Transfer (ICT) with 3,5-Dimethyl-4-(dimethylamino)benzonitrile (MMD) and Its Meta-Isomer mMMD. Ground State Amino Twist Not Essential for ICT.
The journal of physical chemistry. A, 2015, 119, 11820-11836
1540572 CIFC15 H22 N2P 1 21 18.4033; 8.2068; 10.092
90; 92.33; 90
695.4Druzhinin, Sergey I.; Galievsky, Victor A.; Demeter, Attila; Kovalenko, Sergey A.; Senyushkina, Tamara; Dubbaka, Srinivas R.; Knochel, Paul; Mayer, Peter; Grosse, Christian; Stalke, Dietmar; Zachariasse, Klaas A.
Two-State Intramolecular Charge Transfer (ICT) with 3,5-Dimethyl-4-(dimethylamino)benzonitrile (MMD) and Its Meta-Isomer mMMD. Ground State Amino Twist Not Essential for ICT.
The journal of physical chemistry. A, 2015, 119, 11820-11836
1540573 CIFC12 H12 N2P -16.575; 7.956; 9.875
90.42; 107.21; 101.99
481.4Druzhinin, Sergey I.; Galievsky, Victor A.; Demeter, Attila; Kovalenko, Sergey A.; Senyushkina, Tamara; Dubbaka, Srinivas R.; Knochel, Paul; Mayer, Peter; Grosse, Christian; Stalke, Dietmar; Zachariasse, Klaas A.
Two-State Intramolecular Charge Transfer (ICT) with 3,5-Dimethyl-4-(dimethylamino)benzonitrile (MMD) and Its Meta-Isomer mMMD. Ground State Amino Twist Not Essential for ICT.
The journal of physical chemistry. A, 2015, 119, 11820-11836
1540574 CIFC15 H11 N O3P 1 21/n 112.134; 7.418; 26.1516
90; 91.845; 90
2352.69Tomás-Mendivil, Eder; Starck, Jérôme; Ortuno, Jean-Claude; Michelet, Véronique
Synthesis of Functionalized 1H-Isochromene Derivatives via a Au-Catalyzed Domino Cycloisomerization/Reduction Approach.
Organic letters, 2015, 17, 6126-6129
1540575 CIF
HKL
Ca Gd2 Mo4 O16I 41/a :25.22344; 5.22344; 11.50019
90; 90; 90
313.77Chang Sung Lim; Victor Atuchin; Aleksandr Aleksandrovsky; Maxim Molokeev; Aleksandr Oreshonkov
Microwave sol-gel synthesis of CaGd2(MoO4)4:Er3+/Yb3+ phosphors and their upconversion photoluminescence properties
Journal of the American Ceramic Society, 2015, 98, 3223-3230
1540576 CIF
HKL
Ca Er0.2 Gd1.8 Mo4 O16I 41/a :25.21601; 5.21601; 11.4875
90; 90; 90
312.54Chang Sung Lim; Victor Atuchin; Aleksandr Aleksandrovsky; Maxim Molokeev; Aleksandr Oreshonkov
Microwave sol-gel synthesis of CaGd2(MoO4)4:Er3+/Yb3+ phosphors and their upconversion photoluminescence properties
Journal of the American Ceramic Society, 2015, 98, 3223-3230
1540577 CIF
HKL
Ca Er0.1 Gd1.7 Mo4 O16 Yb0.2I 41/a :25.21412; 5.21412; 11.48095
90; 90; 90
312.13Chang Sung Lim; Victor Atuchin; Aleksandr Aleksandrovsky; Maxim Molokeev; Aleksandr Oreshonkov
Microwave sol-gel synthesis of CaGd2(MoO4)4:Er3+/Yb3+ phosphors and their upconversion photoluminescence properties
Journal of the American Ceramic Society, 2015, 98, 3223-3230
1540578 CIF
HKL
Ca Er0.05 Gd1.5 Mo4 O16 Yb0.45I 41/a :25.21103; 5.21103; 11.47435
90; 90; 90
311.58Chang Sung Lim; Victor Atuchin; Aleksandr Aleksandrovsky; Maxim Molokeev; Aleksandr Oreshonkov
Microwave sol-gel synthesis of CaGd2(MoO4)4:Er3+/Yb3+ phosphors and their upconversion photoluminescence properties
Journal of the American Ceramic Society, 2015, 98, 3223-3230
1540580 CIFC34 H30 O2P 6526.2091; 26.2091; 6.7076
90; 90; 120
3990.3Kumar, Ravindra; Tokura, Hiromu; Nishimura, Akira; Mori, Tadashi; Hoshimoto, Yoichi; Ohashi, Masato; Ogoshi, Sensuke
Nickel(0)/N-Heterocyclic Carbene-Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of Two Enones and an Alkyne: Access to Cyclohexenes with Four Contiguous Stereogenic Centers.
Organic letters, 2015, 17, 6018-6021
1540584 CIFC21 H29 N O7P -16.1386; 8.845; 20.0476
100.943; 95.193; 92.11
1062.7Cameron, Alex; Fisher, Brendan; Fisk, Nicholas; Hummel, Jessica; White, Jonathan M.; Krenske, Elizabeth H.; Rizzacasa, Mark A.
Towards the Synthesis of Dihydrooxepino[4,3-b]pyrrole-Containing Natural Products via Cope Rearrangement of Vinyl Pyrrole Epoxides.
Organic letters, 2015, 17, 5998-6001
1540588 CIFC58 H72 Br4 N9 O10 YbP 1 21/n 116.2698; 15.1873; 25.1775
90; 96.682; 90
6179Decortes, Antonello; Haak, Robert M.; Martín, Carmen; Belmonte, Marta Martínez; Martin, Eddy; Benet-Buchholz, Jordi; Kleij, Arjan W.
Copolymerization of CO2and Cyclohexene Oxide Mediated by Yb(salen)-Based Complexes
Macromolecules, 2015, 48, 8197
1540589 CIFC40 H47 N2 O5 YbP 21 21 2113.3478; 15.5479; 17.2278
90; 90; 90
3575.29Decortes, Antonello; Haak, Robert M.; Martín, Carmen; Belmonte, Marta Martínez; Martin, Eddy; Benet-Buchholz, Jordi; Kleij, Arjan W.
Copolymerization of CO2and Cyclohexene Oxide Mediated by Yb(salen)-Based Complexes
Macromolecules, 2015, 48, 8197
1540590 CIFC15 H7 F O2P -17.2431; 9.1369; 9.4709
67.245; 89.096; 67.767
528.73Wu, Xunshen; Yang, Yang; Han, Jianwei; Wang, Limin
Palladium Catalyzed C-I and Vicinal C-H Dual Activation of Diaryliodonium Salts for Diarylation: Synthesis of 4,5-Benzocoumarins.
Organic letters, 2015, 17, 5654-5657
1540591 CIFC23 H31 N O2P 1 21/c 112.335; 13.08; 12.657
90; 102.79; 90
1991.4Wang, Xinbo; Pan, Yupeng; Huang, Kuo-Wei; Lai, Zhiping
One-Pot Synthesis of N-(α-Peroxy)Indole/Carbazole via Chemoselective Three-Component Condensation Reaction in Open Atmosphere.
Organic letters, 2015, 17, 5630-5633
1540592 CIFC12 H12 O2P 1 21/c 111.418; 10.794; 17.585
90; 102.207; 90
2118Mao, Wenbin; Zhu, Chen
Synergistic Acid-Promoted Synthesis of Highly Substituted Butenolides via the Annulation of Keto Acids and Tertiary Alcohols.
Organic letters, 2015, 17, 5710-5713
1540593 CIFC33 H24 F3 N O4 SP -114.2696; 14.853; 14.948
67.375; 72.768; 89.623
2772.3Nayak, Sanatan; Ghosh, Nayan; Prabagar, B.; Sahoo, Akhila K.
p-TsOH Promoted Au(I)-Catalyzed Consecutive Endo Cyclization of Yne-Tethered Ynamide: Access to Benzofused Dihydroisoquinolones.
Organic letters, 2015, 17, 5662-5665
1540594 CIFC21 H16 O4P b c a11.3289; 14.3997; 19.8404
90; 90; 90
3236.6Zheng, Yang; Mao, Jincheng; Weng, Yuecheng; Zhang, Xiaolu; Xu, Xinfang
Cyclopentadiene Construction via Rh-Catalyzed Carbene/Alkyne Metathesis Terminated with Intramolecular Formal [3 + 2] Cycloaddition.
Organic letters, 2015, 17, 5638-5641
1540595 CIFC15 H15 N O4 SP 21 21 218.1024; 11.3536; 14.828
90; 90; 90
1364Kong, Jongrock; McLaughlin, Mark; Belyk, Kevin; Mondschein, Ryan
Enantioselective Rh(I)-Catalyzed Addition of Arylboronic Acids to Cyclic Ketimines.
Organic letters, 2015, 17, 5520-5523
1540596 CIFC20 H16 Br N O4P 21 21 218.1709; 8.6771; 25.4706
90; 90; 90
1805.86Skrzyńska, Anna; Przydacz, Artur; Albrecht, Łukasz
Organocatalytic Nonclassical Trienamine Activation in the Remote Alkylation of Furan Derivatives.
Organic letters, 2015, 17, 5682-5685
1540597 CIFC22 H15 Cl F3 N O3 SP 1 21/n 110.3902; 11.1304; 17.5579
90; 95.9749; 90
2019.49Huang, Zhongyan; Wang, Chen; Tokunaga, Etsuko; Sumii, Yuji; Shibata, Norio
Stereoselective Synthesis of β-Lactam-triflones under Catalyst-Free Conditions.
Organic letters, 2015, 17, 5610-5613
1540598 CIFC21 H21 N SiP -110.2204; 10.3756; 18.4485
95.235; 105.12; 108.782
1754.9Hao, Wei; Wang, Han; Ye, Qingyu; Zhang, Wen-Xiong; Xi, Zhenfeng
Cyclopentadiene-Phosphine/Palladium-Catalyzed Synthesis of Indolizines from Pyrrole and 1,4-Dibromo-1,3-butadienes.
Organic letters, 2015, 17, 5674-5677
1540599 CIFC23 H17 N O3P 21 21 217.2793; 12.9826; 18.8537
90; 90; 90
1781.8Banerjee, Arghya; Santra, Sourav Kumar; Mohanta, Prakash Ranjan; Patel, Bhisma K.
Ruthenium(II) Catalyzed Regiospecific C-H/O-H Annulations of Directing Arenes via Weak Coordination.
Organic letters, 2015, 17, 5678-5681
1540600 CIFC29 H18 Cl N OP -19.6188; 10.5071; 11.1216
94.256; 104.939; 102.615
1049.6Banerjee, Arghya; Santra, Sourav Kumar; Mohanta, Prakash Ranjan; Patel, Bhisma K.
Ruthenium(II) Catalyzed Regiospecific C-H/O-H Annulations of Directing Arenes via Weak Coordination.
Organic letters, 2015, 17, 5678-5681
1540601 CIFC20 H21 N O2P n a 217.5747; 10.8659; 20.7341
90; 90; 90
1706.54Karmakar, Raju; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Ni(II)-Catalyzed Highly Stereo- and Regioselective Syntheses of Isoindolinones and Isoquinolinones from in Situ Prepared Aldimines Triggered by Homoallylation/Lactamization Cascade.
Organic letters, 2015, 17, 5650-5653
1540602 CIFC13 H12 O2P -18.1069; 8.3799; 8.9188
102.823; 100.864; 113.21
516.59Sekine, Kohei; Sadamitsu, Yuta; Yamada, Tohru
SilverCatalyzed Cascade Carboxylation and Cyclization of Trimethyl(2-methylenebut-3-yn-1-yl)silane Derivatives.
Organic letters, 2015, 17, 5706-5709
1540603 CIFC15 H12 B N3 OP c a 217.6982; 5.5273; 29.041
90; 90; 90
1235.7Adachi, Shinya; Liew, Sean K.; Lee, C. Frank; Lough, Alan; He, Zhi; Denis, Jeffrey D St; Poda, Gennady; Yudin, Andrei K.
Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach.
Organic letters, 2015, 17, 5594-5597
1540604 CIFC15 H13 B N4P b c a10.6778; 8.9179; 27.039
90; 90; 90
2574.75Adachi, Shinya; Liew, Sean K.; Lee, C. Frank; Lough, Alan; He, Zhi; Denis, Jeffrey D St; Poda, Gennady; Yudin, Andrei K.
Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach.
Organic letters, 2015, 17, 5594-5597
1540605 CIFC38 H25 O PP -110.332; 10.435; 13.632
67.996; 82.773; 76.624
1324.5Wu, Bin; Chopra, Rena; Yoshikai, Naohiko
One-Pot Benzo[b]phosphole Synthesis through Sequential Alkyne Arylmagnesiation, Electrophilic Trapping, and Intramolecular Phospha-Friedel-Crafts Cyclization.
Organic letters, 2015, 17, 5666-5669
1540606 CIFC12 H17 N O3 S2P 21 21 218.7469; 13.4624; 24.6866
90; 90; 90
2906.95Marsini, Maurice A.; Reeves, Jonathan T.; Desrosiers, Jean-Nicolas; Herbage, Melissa A.; Savoie, Jolaine; Li, Zhibin; Fandrick, Keith R.; Sader, C. Avery; McKibben, Bryan; Gao, Donghong A.; Cui, Jianwen; Gonnella, Nina C.; Lee, Heewon; Wei, Xudong; Roschangar, Frank; Lu, Bruce Z.; Senanayake, Chris H.
Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters.
Organic letters, 2015, 17, 5614-5617
1540607 CIFC15 H21 N O3 SP 21 21 215.9251; 14.3949; 17.8151
90; 90; 90
1519.47Marsini, Maurice A.; Reeves, Jonathan T.; Desrosiers, Jean-Nicolas; Herbage, Melissa A.; Savoie, Jolaine; Li, Zhibin; Fandrick, Keith R.; Sader, C. Avery; McKibben, Bryan; Gao, Donghong A.; Cui, Jianwen; Gonnella, Nina C.; Lee, Heewon; Wei, Xudong; Roschangar, Frank; Lu, Bruce Z.; Senanayake, Chris H.
Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters.
Organic letters, 2015, 17, 5614-5617
1540608 CIFC32 H37 Br Cl N3 O6 S2P 19.9554; 13.0776; 14.9103
75.045; 78.893; 69.659
1747.12Marsini, Maurice A.; Reeves, Jonathan T.; Desrosiers, Jean-Nicolas; Herbage, Melissa A.; Savoie, Jolaine; Li, Zhibin; Fandrick, Keith R.; Sader, C. Avery; McKibben, Bryan; Gao, Donghong A.; Cui, Jianwen; Gonnella, Nina C.; Lee, Heewon; Wei, Xudong; Roschangar, Frank; Lu, Bruce Z.; Senanayake, Chris H.
Diastereoselective Synthesis of α-Quaternary Aziridine-2-carboxylates via Aza-Corey-Chaykovsky Aziridination of N-tert-Butanesulfinyl Ketimino Esters.
Organic letters, 2015, 17, 5614-5617
1540609 CIFC20 H20 N2 O SP 1 21/n 110.5944; 5.6765; 27.958
90; 94.681; 90
1675.8Zhu, Longzhi; Qiu, Renhua; Cao, Xin; Xiao, Song; Xu, Xinhua; Au, Chak-Tong; Yin, Shuang-Feng
Copper-Mediated Remote C-H Bond Chalcogenation of Quinolines on the C5 Position.
Organic letters, 2015, 17, 5528-5531
1540610 CIFC23 H30 N2 O4 SP 1 21/n 17.7796; 34.171; 8.2694
90; 93.715; 90
2193.7Shen, Mei-Hua; Xu, Ke; Sun, Chu-Han; Xua, Hua-Dong
Stereoselective Construction of Bridged trans-aza-Bicyclo[7/6,3/2,1]alkenyl Imines through Ring Expansion aza-Cope Rearrangement.
Organic letters, 2015, 17, 5598-5601
1540611 CIFC60 H56 Si4P b c a16.685; 16.536; 37.285
90; 90; 90
10287Fu, Xiangyu; Zhao, Dahui
Cyclo-oligomerization of 6,12-Diethynyl Indeno[1,2-b]fluorenes via Diradical Intermediates.
Organic letters, 2015, 17, 5694-5697
1540612 CIFC20 H22 O4P 1 21/n 18.1446; 8.8894; 22.8882
90; 97.4066; 90
1643.29Mackay, Emily G.; Nörret, Marck; Wong, Leon S.-M.; Louis, Ignace; Lawrence, Andrew L.; Willis, Anthony C.; Sherburn, Michael S.
A Domino Diels-Alder Approach toward the Tetracyclic Nicandrenone Framework.
Organic letters, 2015, 17, 5517-5519
1540613 CIFC20 H22 O4P 1 21/c 114.271; 7.3032; 15.87
90; 97.862; 90
1638.5Mackay, Emily G.; Nörret, Marck; Wong, Leon S.-M.; Louis, Ignace; Lawrence, Andrew L.; Willis, Anthony C.; Sherburn, Michael S.
A Domino Diels-Alder Approach toward the Tetracyclic Nicandrenone Framework.
Organic letters, 2015, 17, 5517-5519
1540614 CIFC15 H14 N2 O7P -16.8857; 7.8782; 14.23
73.669; 85.904; 80.621
730.62Wagner, Frederic; Harms, Klaus; Koert, Ulrich
Hauser-Heck: Efficient Synthesis of γ-Aryl-β-ketoesters en Route to Substituted Naphthalenes.
Organic letters, 2015, 17, 5670-5673
1540615 CIFC13 H10 N2 O7P -16.4851; 8.2205; 12.0587
92.463; 91.458; 99.303
633.47Wagner, Frederic; Harms, Klaus; Koert, Ulrich
Hauser-Heck: Efficient Synthesis of γ-Aryl-β-ketoesters en Route to Substituted Naphthalenes.
Organic letters, 2015, 17, 5670-5673
1540616 CIFC15 H16 O5P -17.9292; 8.4053; 10.7094
93.039; 104.73; 106.745
654.85Wagner, Frederic; Harms, Klaus; Koert, Ulrich
Hauser-Heck: Efficient Synthesis of γ-Aryl-β-ketoesters en Route to Substituted Naphthalenes.
Organic letters, 2015, 17, 5670-5673
1540617 CIFC30 H26 O3 SP 1 n 114.188; 5.8892; 15.3276
90; 103.795; 90
1243.77Chang, Meng-Yang; Cheng, Yu-Chieh
Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.
Organic letters, 2015, 17, 5702-5705
1540618 CIFC24 H20 O2P -17.1637; 11.4472; 11.9023
79.27; 77.811; 87.147
937.3Chang, Meng-Yang; Cheng, Yu-Chieh
Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.
Organic letters, 2015, 17, 5702-5705
1540619 CIFC24 H21 F O3 SP 1 21/n 115.3544; 5.9154; 21.8657
90; 90.554; 90
1985.91Chang, Meng-Yang; Cheng, Yu-Chieh
Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.
Organic letters, 2015, 17, 5702-5705
1540620 CIFC30 H26 O3 SP c a 2116.1272; 8.2497; 17.782
90; 90; 90
2365.8Chang, Meng-Yang; Cheng, Yu-Chieh
Bi(OTf)3 Mediated exo-Olefin Isomerization of α-Benzoyl β-Styrylsulfones.
Organic letters, 2015, 17, 5702-5705
1540621 CIFC14 H11 Br N4 OP 1 21/c 114.7522; 13.9738; 6.7673
90; 100.152; 90
1373.2Rajamanickam, Suresh; Majji, Ganesh; Santra, Sourav Kumar; Patel, Bhisma K.
Bu4NI Catalyzed C-N Bond Formation via Cross-Dehydrogenative Coupling of Aryl Ethers (Csp3-H) and Tetrazoles (N-H).
Organic letters, 2015, 17, 5586-5589
1540622 CIFC27 H20 Cl F3 N2 O3C 1 2 119.9301; 11.6169; 12.0116
90; 106.035; 90
2672.8Zhou, Ding; Huang, Zheng; Yu, Xueting; Wang, Youxin; Li, Jian; Wang, Wei; Xie, Hexin
A Quinine-Squaramide Catalyzed Enantioselective Aza-Friedel-Crafts Reaction of Cyclic Trifluoromethyl Ketimines with Naphthols and Electron-Rich Phenols.
Organic letters, 2015, 17, 5554-5557
1540623 CIFC17 H17 N OP n m a17.598; 6.875; 10.631
90; 90; 90
1286.2Das, Sajal; Hong, Dongsub; Chen, Zhiwei; She, Zhigang; Hersh, William H.; Subramaniam, Gopal; Chen, Yu
Auto-Tandem Palladium Catalysis: From Isoxazole to 2-Azafluorenone.
Organic letters, 2015, 17, 5578-5581
1540624 CIFC17 H19 N O2P 1 21/c 19.5944; 19.75; 7.917
90; 90.554; 90
1500.1Das, Sajal; Hong, Dongsub; Chen, Zhiwei; She, Zhigang; Hersh, William H.; Subramaniam, Gopal; Chen, Yu
Auto-Tandem Palladium Catalysis: From Isoxazole to 2-Azafluorenone.
Organic letters, 2015, 17, 5578-5581
1540625 CIFC32 H21 O5 P WP 1 21/c 111.521; 11.9824; 20.383
90; 98.02; 90
2786.34Zhou, Yang; Gan, Zhenjie; Su, Bo; Li, Jun; Duan, Zheng; Mathey, François
Intramolecular, Pd/Cu-Co-catalyzed P-C Bond Cleavage and Addition onto an Alkyne: A Route to Benzophospholes.
Organic letters, 2015, 17, 5722-5724
1540626 CIFC54 H78 Mo N2 O2P 110.0435; 10.3143; 12.8862
74.5019; 87.313; 78.6415
1261.15Al-Khafaji, Yahya; Prior, Timothy; Elsegood, Mark; Redshaw, Carl
Molybdenum (VI) Imido Complexes Derived from Chelating Phenols: Synthesis, Characterization and ɛ-Caprolactone ROP Capability
Catalysts, 2015, 5, 1928
1540627 CIFC60 H82 Cl2 Mo N2 O2P -111.7691; 14.1045; 18.0657
83.543; 81.066; 74.829
2851.1Al-Khafaji, Yahya; Prior, Timothy; Elsegood, Mark; Redshaw, Carl
Molybdenum (VI) Imido Complexes Derived from Chelating Phenols: Synthesis, Characterization and ɛ-Caprolactone ROP Capability
Catalysts, 2015, 5, 1928
1540628 CIFC80 H106 F10 Mo2 N4 O4P 1 21/n 114.2727; 15.4944; 18.0242
90; 98.4505; 90
3942.7Al-Khafaji, Yahya; Prior, Timothy; Elsegood, Mark; Redshaw, Carl
Molybdenum (VI) Imido Complexes Derived from Chelating Phenols: Synthesis, Characterization and ɛ-Caprolactone ROP Capability
Catalysts, 2015, 5, 1928
1540629 CIFC114 H158 Mo2 N10 O8P -113.0178; 13.4853; 16.9177
106.113; 96.4972; 92.7062
2825.3Al-Khafaji, Yahya; Prior, Timothy; Elsegood, Mark; Redshaw, Carl
Molybdenum (VI) Imido Complexes Derived from Chelating Phenols: Synthesis, Characterization and ɛ-Caprolactone ROP Capability
Catalysts, 2015, 5, 1928
1540630 CIFC124 H182 Mo2 N4 O4C 1 2/c 140.815; 17.0938; 16.3488
90; 94.82; 90
11365.9Al-Khafaji, Yahya; Prior, Timothy; Elsegood, Mark; Redshaw, Carl
Molybdenum (VI) Imido Complexes Derived from Chelating Phenols: Synthesis, Characterization and ɛ-Caprolactone ROP Capability
Catalysts, 2015, 5, 1928
1540631 CIFC104 H140 F10 Mo2 N8 O8P -118.7522; 22.6704; 25.8469
79.933; 81.162; 81.434
10605.9Al-Khafaji, Yahya; Prior, Timothy; Elsegood, Mark; Redshaw, Carl
Molybdenum (VI) Imido Complexes Derived from Chelating Phenols: Synthesis, Characterization and ɛ-Caprolactone ROP Capability
Catalysts, 2015, 5, 1928
1540632 CIFC28 H44 Cl2 Mo N2 O2P -110.0491; 10.6022; 15.6133
92.902; 90.577; 112.932
1529.2Al-Khafaji, Yahya; Prior, Timothy; Elsegood, Mark; Redshaw, Carl
Molybdenum (VI) Imido Complexes Derived from Chelating Phenols: Synthesis, Characterization and ɛ-Caprolactone ROP Capability
Catalysts, 2015, 5, 1928
1540633 CIFC26 H31 Br N2 O7 SP 1 21/n 110.418; 14.7052; 17.8673
90; 99.129; 90
2702.6Mizoguchi, Kenji; Sakamoto, Hirokazu
Role ofWater Molecules to the Electronic States of M-DNA
Crystals, 2015, 5, 475
1540634 CIFC26 H29 Br N2 O7 SP -18.3812; 13.0305; 13.2656
64.054; 83.078; 86.643
1293.2Mizoguchi, Kenji; Sakamoto, Hirokazu
Role ofWater Molecules to the Electronic States of M-DNA
Crystals, 2015, 5, 475
1540635 CIFC48 H54 Br2 N4 O10 S2P 1 21/n 115.9728; 14.008; 22.8933
90; 109.716; 90
4822Mizoguchi, Kenji; Sakamoto, Hirokazu
Role ofWater Molecules to the Electronic States of M-DNA
Crystals, 2015, 5, 475
1540636 CIFC32 H34 Cu0 N4 O8 ZnP 1 21 111.421; 9.2213; 15.188
90; 106.112; 90
1536.7Tai, Xi-Shi; You, Hai-Ying
A New 1D Chained Coordination Polymer: Synthesis, Crystal Structure, Antitumor Activity and Luminescent Property
Crystals, 2015, 5, 608
1540637 CIFC56 H92 Cl2 N8 Nd2 O2P -110.049; 11.337; 14.471
82.53; 83.02; 73.74
1563Sroor, Farid; Hrib, Cristian; Edelmann, Frank
New Lanthanide Alkynylamidinates and Diiminophosphinates
Inorganics, 2015, 3, 429
1540638 CIFC38 H54 Li2 N4 O2P -19.6687; 9.948; 19.611
93.77; 91.33; 90.96
1881.4Sroor, Farid; Hrib, Cristian; Edelmann, Frank
New Lanthanide Alkynylamidinates and Diiminophosphinates
Inorganics, 2015, 3, 429
1540639 CIFC50 H70 Li2 N4 O2P -19.8768; 10.2082; 11.6883
104.144; 90.248; 104.209
1105.18Sroor, Farid; Hrib, Cristian; Edelmann, Frank
New Lanthanide Alkynylamidinates and Diiminophosphinates
Inorganics, 2015, 3, 429
1540640 CIFC44 H72 Ce Cl2 Li N4 O2 P2 Si4P 1 21/n 111.117; 36.425; 13.538
90; 96.7; 90
5444.6Sroor, Farid; Hrib, Cristian; Edelmann, Frank
New Lanthanide Alkynylamidinates and Diiminophosphinates
Inorganics, 2015, 3, 429
1540641 CIFC16 H18.37 N4 O7.68 YP b c a14.6954; 14.3307; 18.2161
90; 90; 90
3836.2Loukopoulos, Edward; Griffiths, Kieran; Akien, Geoffrey; Kourkoumelis, Nikolaos; Abdul-Sada, Alaa; Kostakis, George
Dinuclear Lanthanide (III) Coordination Polymers in a Domino Reaction
Inorganics, 2015, 3, 448
1540642 CIFC42 H36 Cl3 Dy2 N9 O9P 1 21/n 114.2871; 19.9839; 20.0637
90; 101.857; 90
5606.2Loukopoulos, Edward; Griffiths, Kieran; Akien, Geoffrey; Kourkoumelis, Nikolaos; Abdul-Sada, Alaa; Kostakis, George
Dinuclear Lanthanide (III) Coordination Polymers in a Domino Reaction
Inorganics, 2015, 3, 448

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