Crystallography Open Database

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7157230 CIFC24 H23 N O3 SP 1 21/n 19.6018; 12.4113; 16.8115
90; 96.978; 90
1988.6Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157229 CIFC22 H16 O3 SP 1 21/n 18.8058; 20.394; 9.6437
90; 99.794; 90
1706.6Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157228 CIFC23 H25 N O4 SP 1 21/n 111.6856; 14.0485; 13.2869
90; 96.0216; 90
2169.2Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157227 CIFC23 H23 N3 O2I 41/a :238.315; 38.315; 5.547
90; 90; 90
8143.2Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157226 CIFC17 H12 O5 S2P 1 21/c 18.7498; 18.5113; 9.4511
90; 99.3488; 90
1510.46Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157225 CIFC24 H24 N4 O2P -19.145; 11.501; 11.649
117.55; 94.48; 91.05
1080.9Aiken, Stuart; Anozie, Kelechi; de Azevedo, Orlando D. C. C.; Cowen, Lewis; Edgar, Ross J. L.; Gabbutt, Christopher D.; Heron, B. Mark; Lawrence, Philippa A.; Mills, Abby J.; Rice, Craig R.; Urquhart, Mike W. J.; Zonidis, Dimitrios
Expedient synthesis of highly substituted 3,4-dihydro-1,2-oxathiine 2,2-dioxides and 1,2-oxathiine 2,2-dioxides: revisiting sulfene additions to enaminoketones.
Organic & biomolecular chemistry, 2019, 17, 9585-9604
7157189 CIFC32 H32 N2 O7P 21 21 2113; 13.405; 17.492
90; 90; 90
3048Sharma, Arun; Sharma, Vivek; Chimni, Swapandeep Singh
Organocatalytic enantioselective conjugate addition of pyrazolin-5-ones to arylomethylidene malonates.
Organic & biomolecular chemistry, 2019, 17, 9514
7157188 CIFC12 H13 Br O3P 1 21 15.845; 7.6852; 12.8843
90; 100.457; 90
569.15Shit, Sudip; Devi, Namita; Devi, Ngangbam Renubala; Saikia, Anil K.
Stereoselective synthesis of hexahydrofuro[3,4-b]furan-4-ol and its dimer via tandem Prins and pinacol rearrangement.
Organic & biomolecular chemistry, 2019, 17, 7398-7407
7157187 CIFC24 H24 Br2 O5P 21 21 2117.353; 24.435; 5.4165
90; 90; 90
2296.7Shit, Sudip; Devi, Namita; Devi, Ngangbam Renubala; Saikia, Anil K.
Stereoselective synthesis of hexahydrofuro[3,4-b]furan-4-ol and its dimer via tandem Prins and pinacol rearrangement.
Organic & biomolecular chemistry, 2019, 17, 7398-7407
7157186 CIFC14 H17 F6 N3 OP b c a11.65; 18.43; 15.238
90; 90; 90
3272Moraes, Paulo A.; Lobo, Marcio M.; Marangoni, Mário A; Meyer, Alexandre R.; Frizzo, Clarissa P.; Bonacorso, Helio G.; Martins, Marcos A. P.; Zanatta, Nilo
Chemo- and regioselective reactions of 5-bromo enones/enaminones with pyrazoles.
Organic & biomolecular chemistry, 2019, 17, 2384-2392
7157185 CIFC14 H15 F6 N3 OP 1 21/n 111.79; 7.792; 16.696
90; 103.74; 90
1489.9Moraes, Paulo A.; Lobo, Marcio M.; Marangoni, Mário A; Meyer, Alexandre R.; Frizzo, Clarissa P.; Bonacorso, Helio G.; Martins, Marcos A. P.; Zanatta, Nilo
Chemo- and regioselective reactions of 5-bromo enones/enaminones with pyrazoles.
Organic & biomolecular chemistry, 2019, 17, 2384-2392
7157184 CIFC19 H16 N2 SP 1 21/n 18.5086; 17.1346; 22.5907
90; 99.192; 90
3251.2Zhang, Xi; Wang, Tong-Lin; Liu, Xiao-Jun; Wang, Xi-Cun; Quan, Zheng-Jun
The solvent-controlled chemoselective construction of C-S/S-S bonds via the Michael reaction/thiol coupling of quinoline-2-thiones.
Organic & biomolecular chemistry, 2019, 17, 2379-2383
7157183 CIFC29 H22 N2 O3 SP -112.875; 13.03; 15.195
76.583; 78.566; 72.177
2338.2Kundal, Sandip; Chakraborty, Baitan; Paul, Kartick; Jana, Umasish
Efficient two-step synthesis of structurally diverse indolo[2,3-b]quinoline derivatives.
Organic & biomolecular chemistry, 2019, 17, 2321-2325
7157182 CIFC25 H21 N O3P 1 21/c 111.065; 11.521; 15.832
90; 97.78; 90
1999.68Zeng, Qian; Dong, Kuiyong; Huang, Jingjing; Qiu, Lihua; Xu, Xinfang
Copper-catalyzed carbene/alkyne metathesis terminated with the Buchner reaction: synthesis of dihydrocyclohepta[b]indoles.
Organic & biomolecular chemistry, 2019, 17, 2326-2330
7157181 CIFC24 H36 Cl N3 O Pd SeR -3 :H27.319; 27.319; 19.5324
90; 90; 120
12624.5Sharma, Kamal Nayan; Satrawala, Naveen; Srivastava, Avinash Kumar; Ali, Munsaf; Joshi, Raj Kumar
Palladium(ii) ligated with a selenated (Se, C<sub>NHC</sub>, N<sup>-</sup>)-type pincer ligand: an efficient catalyst for Mizoroki-Heck and Suzuki-Miyaura coupling in water.
Organic & biomolecular chemistry, 2019, 17, 8969-8976
7157159 CIFC24 H26 N2 O3P -111.7236; 11.754; 17.2404
73.252; 73.789; 71.074
2106.24He, Yi; Narmon, Thomas; Wu, Danjun; Li, Zhenghua; Van Meervelt, Luc; Van der Eycken, Erik V.
A gold-triggered dearomative spirocarbocyclization/Diels-Alder reaction cascade towards diverse bridged N-heterocycles.
Organic & biomolecular chemistry, 2019, 17, 9529
7157158 CIFC25 H28 N2 O3P 1 21/n 113.4238; 10.0908; 16.9778
90; 96.486; 90
2285.04He, Yi; Narmon, Thomas; Wu, Danjun; Li, Zhenghua; Van Meervelt, Luc; Van der Eycken, Erik V.
A gold-triggered dearomative spirocarbocyclization/Diels-Alder reaction cascade towards diverse bridged N-heterocycles.
Organic & biomolecular chemistry, 2019, 17, 9529
7157157 CIFC16 H13 N O2 SP -16.4036; 7.8241; 14.538
85.37; 89.441; 70.995
686.3You, Guirong; Xi, Dan; Sun, Jian; Hao, Liqiang; Xia, Chengcai
Transition-metal- and oxidant-free three-component reaction of quinoline N-oxides, sodium metabisulfite and aryldiazonium tetrafluoroborates via a dual radical coupling process.
Organic & biomolecular chemistry, 2019, 17, 9479
7157156 CIFC72 H60 N6 Se3P -111.8825; 12.7306; 20.6914
90.924; 101.853; 111.378
2838.3Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157155 CIFC22 H14 F2 N2 SP 1 21/c 19.5114; 15.691; 11.5516
90; 98.966; 90
1702.9Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157154 CIFC22 H16 N2 SeP 1 21/c 19.6424; 15.1758; 11.7826
90; 101.61; 90
1688.9Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157153 CIFC24 H16 N2 O4 SP -18.8175; 10.9212; 10.9295
76.676; 67.685; 89.692
943.5Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157152 CIFC40 H30 N8 O S2P -19.4466; 9.9176; 19.5777
79.604; 86.538; 70.029
1695.59Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157151 CIFC22 H14 N2 OP 1 n 18.7248; 8.5852; 11.534
90; 105.252; 90
833.5Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157150 CIFC28 H20 N4 O4 SP 1 21/c 113.0978; 8.4281; 21.7783
90; 103.164; 90
2340.92Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157149 CIFC22 H18 N2 SP 1 21/c 19.6081; 15.136; 11.7745
90; 101.041; 90
1680.65Patel, Heta A.; Bhanvadia, Viraj J.; Mande, Hemant M.; Zade, Sanjio S.; Patel, Arun L.
Benzochalcogendiazole-based conjugated molecules: investigating the effects of substituents and heteroatom juggling.
Organic & biomolecular chemistry, 2019, 17, 9467
7157148 CIFC23 H26 N2 O3 SP 21 21 219.2149; 11.3488; 19.7251
90; 90; 90
2062.81Luo, Shao-Xiong; Liu, Yanzhou; Lambrecht, Michael J.; Ortwine, Daniel F.; DiPasquale, Antonio G.; Liang, Jun; Wang, Xiaojing; Zbieg, Jason R.; Li, Jun
cis-Selective synthesis of 1,3-disubstituted tetrahydro-β-carbolines from N-sulfonyl N,S-acetals.
Organic & biomolecular chemistry, 2019, 17, 9510
7157147 CIFC25 H24 N2 O2 SP 21 21 219.0518; 12.1315; 18.9731
90; 90; 90
2083.47Luo, Shao-Xiong; Liu, Yanzhou; Lambrecht, Michael J.; Ortwine, Daniel F.; DiPasquale, Antonio G.; Liang, Jun; Wang, Xiaojing; Zbieg, Jason R.; Li, Jun
cis-Selective synthesis of 1,3-disubstituted tetrahydro-β-carbolines from N-sulfonyl N,S-acetals.
Organic & biomolecular chemistry, 2019, 17, 9510
7157145 CIFC27 H24 N2 O5 SP 21 21 218.5917; 13.421; 21.279
90; 90; 90
2453.7Lu, Min; Li, Hong; Zou, Chuncheng; Li, Jianchang; Liu, Chengyu; Sun, Maolin; Ma, Yueyue; Cheng, Ruihua; Ye, Jinxing
Primary amine catalyzed diastereo- and enantioselective Michael reaction of thiazolones and α,β-unsaturated ketones.
Organic & biomolecular chemistry, 2019, 17, 9305-9312
7157144 CIFC46 H45 Br2 N6 O6C 1 2/c 124.8162; 11.0757; 34.2851
90; 100.28; 90
9272.2Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu
Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes.
Organic & biomolecular chemistry, 2019, 17, 9390-9402
7157143 CIFC36 H32 Br2 N6 O6P 1 21/n 115.516; 9.876; 23.035
90; 104.61; 90
3416Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu
Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes.
Organic & biomolecular chemistry, 2019, 17, 9390-9402
7157142 CIFC19 H18 F N3 O3P 1 21/n 119.0038; 7.304; 25.2096
90; 108.964; 90
3309.26Rao, Madhuri P.; Gunaga, Shubha S.; Zuegg, Johannes; Pamarthi, Rambabu; Ganesh, Madhu
Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes.
Organic & biomolecular chemistry, 2019, 17, 9390-9402
7157141 CIFC20 H20 F Fe I O S SiP -17.148; 9.9469; 15.3417
108.069; 97.069; 91.763
1026.4Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157140 CIFC14 H16 F Fe I O SiP 1 21/n 16.7234; 12.3647; 18.5635
90; 91.338; 90
1542.8Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157139 CIFC25 H25 F Fe I O P SiP -18.1007; 10.7372; 14.989
108.19; 93.055; 97.786
1220.8Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157138 CIFC21 H24 F Fe I O2 SiP -18.514; 10.875; 11.472
86.069; 84.834; 82.271
1046.5Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157137 CIFC13 H16 Br F Fe SiP 1 21/c 117.276; 6.8553; 12.095
90; 100.988; 90
1406.2Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157136 CIFC10 H7 Cl F Fe IP 1 21/c 16.6845; 15.913; 10.315
90; 99.375; 90
1082.6Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157135 CIFC26 H26 F Fe I O SiP -18.1302; 10.5516; 14.7688
107.406; 93.634; 98.033
1189.6Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157134 CIFC14 H16 F Fe I O2 SiP 1 21/n 16.7304; 13.738; 17.564
90; 100.433; 90
1597.2Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157133 CIFC19 H20 F Fe I S SiP 1 21/c 18.8626; 11.0153; 20.456
90; 98.537; 90
1974.9Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157132 CIFC10 H7 F Fe I2P 1 21/c 112.21; 28.6668; 6.6319
90; 100.875; 90
2279.6Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157131 CIFC10 H7 Br Cl F FeP 1 21/n 16.5459; 10.4479; 15.037
90; 91.505; 90
1028Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157130 CIFC16 H12 F Fe I SP -17.2; 10.0755; 11.5617
64.721; 78.205; 84.196
742.31Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157129 CIFC22 H21 B F Fe PP b c a12.4583; 14.7599; 20.49
90; 90; 90
3767.8Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157128 CIFC13 H16 Br F Fe SiP 1 21/c 119.502; 11.7498; 13.23
90; 107.235; 90
2895.5Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157127 CIFC16 H20 B F Fe O2P 1 21/n 113.17; 7.7111; 15.613
90; 105.44; 90
1528.4Tazi, Mehdi; Erb, William; Roisnel, Thierry; Dorcet, Vincent; Mongin, Florence; Low, Paul J.
From ferrocene to fluorine-containing penta-substituted derivatives and all points in-between; or, how to increase the available chemical space.
Organic & biomolecular chemistry, 2019, 17, 9352-9359
7157126 CIFC30 H24 F9 N9 O3P -18.042; 10.654; 20.098
84.402; 81.612; 85.682
1692.2You, Yi; Chen, Yueji; You, Chenhui; Wang, Junwen; Weng, Zhiqiang
Synthesis of 3-(tri/difluoromethyl)-1H-1,2,4-triazol-5(4H)-ones via the cyclization of hydrazinecarboxamides with tri/difluoroacetic anhydride.
Organic & biomolecular chemistry, 2019, 17, 9343-9347
7157125 CIFC10 H9 F2 N3 OI 1 2/a 115.8495; 10.2381; 13.1866
90; 104.544; 90
2071.2You, Yi; Chen, Yueji; You, Chenhui; Wang, Junwen; Weng, Zhiqiang
Synthesis of 3-(tri/difluoromethyl)-1H-1,2,4-triazol-5(4H)-ones via the cyclization of hydrazinecarboxamides with tri/difluoroacetic anhydride.
Organic & biomolecular chemistry, 2019, 17, 9343-9347
7157124 CIFC28 H21 Cl N4 OP 21 21 217.6734; 11.9044; 27.0141
90; 90; 90
2467.7Ji, Yan-Ling; Li, He-Ping; Ai, Yue-Yan; Li, Guo; He, Xiang-Hong; Huang, Wei; Huang, Rui-Zhen; Han, Bo
Enantio- and diastereoselective synthesis of spiropyrazolones via an organocatalytic [1 + 2 + 3] multicomponent reaction.
Organic & biomolecular chemistry, 2019, 17, 9217-9225
7157123 CIFC28 H21 Cl N4 OP 21 21 217.5705; 11.9923; 27.772
90; 90; 90
2521.4Ji, Yan-Ling; Li, He-Ping; Ai, Yue-Yan; Li, Guo; He, Xiang-Hong; Huang, Wei; Huang, Rui-Zhen; Han, Bo
Enantio- and diastereoselective synthesis of spiropyrazolones via an organocatalytic [1 + 2 + 3] multicomponent reaction.
Organic & biomolecular chemistry, 2019, 17, 9217-9225
7157122 CIFC19 H15 F3 N O SP b c a11.2395; 9.4816; 32.652
90; 90; 90
3479.7Ansari, Monish Arbaz; Yadav, Dhananjay; Soni, Sonam; Singh, Maya Shankar
Phosphonium ylide catalysis: a divergent diastereoselective approach to synthesize cyclic ketene acetals [thia(zolidines/zinanes)] from β-ketothioamides and dihaloalkanes.
Organic & biomolecular chemistry, 2019, 17, 9151-9162
7157121 CIFC18 H15 N O3 SP -18.5498; 9.8965; 10.498
86.67; 77.284; 65.193
785.94Ansari, Monish Arbaz; Yadav, Dhananjay; Soni, Sonam; Singh, Maya Shankar
Phosphonium ylide catalysis: a divergent diastereoselective approach to synthesize cyclic ketene acetals [thia(zolidines/zinanes)] from β-ketothioamides and dihaloalkanes.
Organic & biomolecular chemistry, 2019, 17, 9151-9162
7157120 CIFC36 H49 N O6 SP 1 21 16.41147; 9.65864; 26.39665
90; 91.6151; 90
1633.99Kiełczewska, Urszula; Morzycki, Jacek W.; Rárová, Lucie; Wojtkielewicz, Agnieszka
The synthesis of solasodine F-homo-analogues.
Organic & biomolecular chemistry, 2019, 17, 9050-9058
7157119 CIFC43 H54 N2 O7P 1 21 16.2833; 33.99155; 8.90762
90; 107.114; 90
1818.25Kiełczewska, Urszula; Morzycki, Jacek W.; Rárová, Lucie; Wojtkielewicz, Agnieszka
The synthesis of solasodine F-homo-analogues.
Organic & biomolecular chemistry, 2019, 17, 9050-9058
7157118 CIFC43 H66 N4 O7P -115.784; 15.892; 21.646
72.44; 76.389; 61.814
4534.9Veeresh, Kuruva; Singh, Manjeet; Gopi, Hosahudya N.
Impact of substituent effects on the design of β-sheet mimetics and β-double helices from (E)-vinylogous γ-amino acid oligomers.
Organic & biomolecular chemistry, 2019, 17, 9226-9231
7157117 CIFC38 H64 N4 O7P 110.0311; 13.762; 14.965
92.146; 95.34; 97.624
2036.1Veeresh, Kuruva; Singh, Manjeet; Gopi, Hosahudya N.
Impact of substituent effects on the design of β-sheet mimetics and β-double helices from (E)-vinylogous γ-amino acid oligomers.
Organic & biomolecular chemistry, 2019, 17, 9226-9231
7157116 CIFC24 H23 Cl N2 O4 S2P -110.622; 10.722; 11.698
78.63; 78.84; 67.46
1196.1Xu, Zhong-Qi; Wang, Wen-Bo; Zheng, Lin-Chuang; Li, Lin; Duan, Lili; Li, Yue-Ming
Iodine-mediated aminosulfonylation of alkenyl sulfonamides with sulfonyl hydrazides: synthesis of sulfonylmethyl piperidines, pyrrolidines and pyrazolines.
Organic & biomolecular chemistry, 2019, 17, 9026-9038
7157115 CIFC20 H24 N2 O6 S2P 1 21/c 111.026; 15.703; 12.684
90; 98.83; 90
2170.1Xu, Zhong-Qi; Wang, Wen-Bo; Zheng, Lin-Chuang; Li, Lin; Duan, Lili; Li, Yue-Ming
Iodine-mediated aminosulfonylation of alkenyl sulfonamides with sulfonyl hydrazides: synthesis of sulfonylmethyl piperidines, pyrrolidines and pyrazolines.
Organic & biomolecular chemistry, 2019, 17, 9026-9038
7157114 CIFC12 H11 Br N2 O2P b c a9.93; 9.524; 24.977
90; 90; 90
2362.2Xu, Kang; Yang, Ruiqi; Yang, Shuang; Jiang, Cheng; Ding, Zhenhua
Hypervalent iodane mediated reactions of N-acetyl enamines for the synthesis of oxazoles and imidazoles.
Organic & biomolecular chemistry, 2019, 17, 8977-8981
7157113 CIFC10 H8 Br N OP -15.6468; 12.0159; 14.1013
81.991; 89.552; 82.145
938.51Xu, Kang; Yang, Ruiqi; Yang, Shuang; Jiang, Cheng; Ding, Zhenhua
Hypervalent iodane mediated reactions of N-acetyl enamines for the synthesis of oxazoles and imidazoles.
Organic & biomolecular chemistry, 2019, 17, 8977-8981
7157112 CIFC35 H36 F2 N4 O4 SP 1 21 111.896; 10.6048; 13.5243
90; 109.984; 90
1603.42Zhou, Yuxuan; Ma, Fanghui; Lu, Ping; Wang, Yanguang
Preparation of spiro[imidazolidine-4,3'-indolin]-2'-imines via copper(i)-catalyzed formal [2 + 2 + 1] cycloaddition of 3-diazoindolin-2-imines and triazines.
Organic & biomolecular chemistry, 2019, 17, 8849-8852
7157111 CIFC19 H17 N3 O3P 1 21/c 116.6547; 13.5081; 16.2182
90; 117.968; 90
3222.5Su, Yiting; Huang, Gaofeng; Ye, Fu; Qiao, Panpan; Ye, Jinxiang; Gao, Yu; Chen, Haijun
Facile access to evodiakine enabled by aerobic copper-catalyzed oxidative rearrangement.
Organic & biomolecular chemistry, 2019, 17, 8811-8815
7157110 CIFC19 H17 N3 O3P 1 21/c 115.3447; 10.116; 10.7205
90; 109.892; 90
1564.82Su, Yiting; Huang, Gaofeng; Ye, Fu; Qiao, Panpan; Ye, Jinxiang; Gao, Yu; Chen, Haijun
Facile access to evodiakine enabled by aerobic copper-catalyzed oxidative rearrangement.
Organic & biomolecular chemistry, 2019, 17, 8811-8815
7157109 CIFC30 H36 Se2 Si2P 21 21 219.4081; 14.8474; 20.854
90; 90; 90
2913Hasegawa, Masashi; Kobayakawa, Kosuke; Nojima, Yuki; Mazaki, Yasuhiro
Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2'-biselenophene and [2.2]paracyclophane.
Organic & biomolecular chemistry, 2019, 17, 8822-8826
7157108 CIFC49 H37 Cl3 Se4P 1 21 19.6143; 16.0071; 13.8424
90; 94.363; 90
2124.1Hasegawa, Masashi; Kobayakawa, Kosuke; Nojima, Yuki; Mazaki, Yasuhiro
Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2'-biselenophene and [2.2]paracyclophane.
Organic & biomolecular chemistry, 2019, 17, 8822-8826
7157107 CIFC26 H46 B2 O4 Se2 Si2P n a 2144.64; 6.5823; 11.7225
90; 90; 90
3444.5Hasegawa, Masashi; Kobayakawa, Kosuke; Nojima, Yuki; Mazaki, Yasuhiro
Synthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2'-biselenophene and [2.2]paracyclophane.
Organic & biomolecular chemistry, 2019, 17, 8822-8826
7157106 CIFC35 H22 O3P -17.4625; 14.4575; 14.4842
111.262; 99.696; 94.536
1418.71Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157105 CIFC34 H19 Br O3P -114.3618; 16.8874; 19.6152
77.2599; 71.5053; 73.2936
4277.2Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157104 CIFC34 H18 Cl4 O3P 1 21/n 16.8857; 16.5875; 24.9506
90; 93.9567; 90
2842.98Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157103 CIFC73 H52 Cl2 N2 O8P -111.4707; 17.0265; 17.1384
68.014; 87.526; 70.835
2919.6Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157102 CIFC35 H22 Br N O4P -19.9903; 12.0129; 12.3878
80.372; 82.962; 68.265
1358.56Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157101 CIFC32 H18 Br N O2P 1 21/c 112.5801; 29.118; 7.2563
90; 98.229; 90
2630.7Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157100 CIFC38 H30 N2 O3P -111.465; 11.89; 12.656
110.391; 108.863; 98.617
1461.8Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157099 CIFC34 H19 Br O3P -112.672; 14.322; 15.13
80.53; 89.793; 68.279
2511.3Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157098 CIFC37 H27 Br N2 O3P -111.5199; 11.9192; 12.6746
109.822; 108.543; 99.91
1473.8Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157097 CIFC34 H19 Cl O3P -17.6023; 14.1593; 14.3949
112.791; 94.3666; 96.6561
1406.45Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157096 CIFC28 H15 Br O3P 1 21/c 116.1126; 14.9541; 8.7949
90; 104.805; 90
2048.8Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157095 CIFC35 H22 Cl N O4P -110.0137; 11.9245; 12.3604
80.619; 82.259; 67.699
1343Cao, Jun; Sun, Jing; Yan, Chao-Guo
Construction of indeno[1,2-a]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones.
Organic & biomolecular chemistry, 2019, 17, 9008-9013
7157094 CIFC24 H29 N O6P 1 21/n 19.932; 12.9438; 18.2127
90; 92.2716; 90
2339.55Kurian, Jais; M, Muraleedharan Kannoth
Synthesis of new cyclazines and 4,5-diaryl-1H-pyrrol-3(2H)-one units in discoipyrroles from indolizinone-DMAD cycloadducts.
Organic & biomolecular chemistry, 2019, 17, 8832-8848
7157093 CIFC36 H34 N2 O4P -111.6409; 11.8981; 12.5461
67.133; 76.352; 89.759
1548.5Kurian, Jais; M, Muraleedharan Kannoth
Synthesis of new cyclazines and 4,5-diaryl-1H-pyrrol-3(2H)-one units in discoipyrroles from indolizinone-DMAD cycloadducts.
Organic & biomolecular chemistry, 2019, 17, 8832-8848
7157092 CIFC27 H23 N O5P -16.0337; 12.7989; 15.3967
83.2254; 79.7254; 82.5173
1154.49Kurian, Jais; M, Muraleedharan Kannoth
Synthesis of new cyclazines and 4,5-diaryl-1H-pyrrol-3(2H)-one units in discoipyrroles from indolizinone-DMAD cycloadducts.
Organic & biomolecular chemistry, 2019, 17, 8832-8848
7157091 CIFC52 H50 N2 O8 S2P 1 21/c 18.3119; 24.2166; 11.0613
90; 93.864; 90
2221.4Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157090 CIFC33 H31 N O5 SP 1 21 19.1034; 9.5264; 15.9591
90; 91.547; 90
1383.51Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157089 CIFC32 H29 N O4 SP 1 21 19.2331; 9.4073; 15.2033
90; 91.611; 90
1320.01Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157088 CIFC33 H31 N O4 SP 1 21/c 19.2545; 9.0908; 32.563
90; 96.115; 90
2724Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157087 CIFC56 H58 N2 O10 S2P -110.605; 16.0358; 16.1366
69.467; 72.006; 89.666
2427.91Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157086 CIFC31 H27 N O4 SP 1 21/c 115.6522; 13.6042; 12.4636
90; 107.449; 90
2531.8Gharpure, Santosh J.; Nanda, Santosh K.; Fartade, Dipak J.
Expeditious diastereoselective synthesis of medium ring heterocycle-fused chromenes via tandem 8/9-endo-dig and 8-exo-dig hydroalkoxylation-formal-[4 + 2] cycloaddition.
Organic & biomolecular chemistry, 2019, 17, 8806-8810
7157085 CIFC25 H26 Cl2 N2 O2P 1 21/n 116.0878; 7.3312; 19.996
90; 101.831; 90
2308.3Amiri, Kamran; Khosravi, Hormoz; Balalaie, Saeed; Golmohammadi, Farhad; Anwar, Muhammad U.; Al-Harrasi, Ahmed
Regio- and chemo-selective cyclization of allenic-Ugi products for the synthesis of 3-pyrroline skeletons.
Organic & biomolecular chemistry, 2019, 17, 8858-8870
7157084 CIFC23 H26 N2 O2P 1 21/n 111.5219; 11.4926; 15.5242
90; 92.72; 90
2053.3Amiri, Kamran; Khosravi, Hormoz; Balalaie, Saeed; Golmohammadi, Farhad; Anwar, Muhammad U.; Al-Harrasi, Ahmed
Regio- and chemo-selective cyclization of allenic-Ugi products for the synthesis of 3-pyrroline skeletons.
Organic & biomolecular chemistry, 2019, 17, 8858-8870
7157083 CIFC23 H23 Br N2 O3 SP 1 21/c 18.7087; 24.853; 10.406
90; 110.876; 90
2104.4Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157082 CIFC21 H16 N2 OP b c a11.2543; 11.6498; 23.6897
90; 90; 90
3105.96Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157081 CIFC21 H17 F N2 O2P 21 21 218.7924; 10.9272; 18.098
90; 90; 90
1738.79Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157080 CIFC50 H52 N4 O4P -112.8963; 13.1501; 17.101
92.305; 111.817; 103.594
2590.69Xu, Yuanshuang; Zhang, Linghua; Liu, Mengyang; Zhang, Xiaopeng; Zhang, Xinying; Fan, Xuesen
Synthesis of benzoazepine derivatives via Rh(iii)-catalyzed inert C(sp<sup>2</sup>)-H functionalization and [4 + 3] annulation.
Organic & biomolecular chemistry, 2019, 17, 8706-8710
7157079 CIFC18 H13 Br O4P 21 21 218.8995; 12.8103; 13.9893
90; 90; 90
1594.85Shi, Taoda; Teng, Shenghan; Gopi Krishna Reddy, Alavala; Guo, Xin; Zhang, Yueteng; Moore, Kohlson T.; Buckley, Thomas; Mason, Damian J.; Wang, Wei; Chapman, Eli; Hu, Wenhao
Catalytic asymmetric synthesis of 2,5-dihydrofurans using synergistic bifunctional Ag catalysis.
Organic & biomolecular chemistry, 2019, 17, 8737-8744
7157078 CIFC16 H14 N2 O3P 1 21/c 17.6987; 11.0695; 16.7175
90; 98.836; 90
1407.77Gupta, Vijay; Sahu, Debashish; Jain, Shailja; Vanka, Kumar; Singh, Ravi P.
Diastereoselective multi-component tandem condensation: synthesis of 2-amino-4-(2-furanone)-4H-chromene-3-carbonitriles.
Organic & biomolecular chemistry, 2019, 17, 8853-8857
7157077 CIFC14 H10 N2 O3P 1 21/c 115.3319; 6.1459; 13.6122
90; 106.075; 90
1232.5Gupta, Vijay; Sahu, Debashish; Jain, Shailja; Vanka, Kumar; Singh, Ravi P.
Diastereoselective multi-component tandem condensation: synthesis of 2-amino-4-(2-furanone)-4H-chromene-3-carbonitriles.
Organic & biomolecular chemistry, 2019, 17, 8853-8857
7157076 CIFC16 H13 Cl3 N2 O3P -18.0552; 10.2825; 11.7512
86.964; 71.0335; 70.4039
865.45Gupta, Vijay; Sahu, Debashish; Jain, Shailja; Vanka, Kumar; Singh, Ravi P.
Diastereoselective multi-component tandem condensation: synthesis of 2-amino-4-(2-furanone)-4H-chromene-3-carbonitriles.
Organic & biomolecular chemistry, 2019, 17, 8853-8857
7157075 CIFC49 H34 Br6 O9 SP -111.4092; 14.1314; 15.9669
109.501; 99.298; 101.718
2301.5Neal, Taylor A.; Neal, Jennifer F.; Eippert, Allyson B.; Moore, Curtis; Allen, Heather C.; Badjić, Jovica D
An easily accessible isospiropyran switch.
Organic & biomolecular chemistry, 2019, 17, 9124-9128
7157074 CIFC16 H11 Br2 Cl O2P -18.6085; 9.1123; 10.0471
74.183; 80.293; 85.184
746.83Neal, Taylor A.; Neal, Jennifer F.; Eippert, Allyson B.; Moore, Curtis; Allen, Heather C.; Badjić, Jovica D
An easily accessible isospiropyran switch.
Organic & biomolecular chemistry, 2019, 17, 9124-9128
7157073 CIFC27 H21 Br3 O4P 1 21/c 111.7759; 8.847; 23.5375
90; 90.994; 90
2451.8Neal, Taylor A.; Neal, Jennifer F.; Eippert, Allyson B.; Moore, Curtis; Allen, Heather C.; Badjić, Jovica D
An easily accessible isospiropyran switch.
Organic & biomolecular chemistry, 2019, 17, 9124-9128
7157072 CIFC31 H29 N3 O5P 1 n 19.394; 10.781; 13.904
90; 106.87; 90
1347.6Zhu, Jindong; Fang, Shuaishuai; Jin, Shiyi; Ma, Rui; Lu, Tao; Du, Ding
Application of isatin-derived saturated esters in the synthesis of 3,3'-spirooxindole γ-butyrolactams.
Organic & biomolecular chemistry, 2019, 17, 8745-8748
7157071 CIFC29 H28 N2 O4C 1 2/c 131.713; 9.7; 18.993
90; 121.61; 90
4976Zhu, Jindong; Fang, Shuaishuai; Jin, Shiyi; Ma, Rui; Lu, Tao; Du, Ding
Application of isatin-derived saturated esters in the synthesis of 3,3'-spirooxindole γ-butyrolactams.
Organic & biomolecular chemistry, 2019, 17, 8745-8748
7157070 CIFC31 H42 Cl2 N2 O4 P2P 41 21 210.7127; 10.7127; 27.9476
90; 90; 90
3207.32Yuan, Minglei; Mbaezue, Ifenna I.; Zhou, Zhi; Topic, Filip; Tsantrizos, Youla S.
P-Chiral, N-phosphoryl sulfonamide Brønsted acids with an intramolecular hydrogen bond interaction that modulates organocatalysis.
Organic & biomolecular chemistry, 2019, 17, 8690-8694
7157069 CIFC10 H12 Br NP 21 21 2116.0321; 6.1532; 9.7828
90; 90; 90
965.06Yuan, Minglei; Mbaezue, Ifenna I.; Zhou, Zhi; Topic, Filip; Tsantrizos, Youla S.
P-Chiral, N-phosphoryl sulfonamide Brønsted acids with an intramolecular hydrogen bond interaction that modulates organocatalysis.
Organic & biomolecular chemistry, 2019, 17, 8690-8694
7157068 CIFC30 H44 N O5 P SP 21 21 2110.584; 15.7917; 18.4493
90; 90; 90
3083.6Yuan, Minglei; Mbaezue, Ifenna I.; Zhou, Zhi; Topic, Filip; Tsantrizos, Youla S.
P-Chiral, N-phosphoryl sulfonamide Brønsted acids with an intramolecular hydrogen bond interaction that modulates organocatalysis.
Organic & biomolecular chemistry, 2019, 17, 8690-8694
7157067 CIFC25 H38 N O4 P SP 1 21 110.679; 12.0178; 11.2241
90; 112.326; 90
1332.5Yuan, Minglei; Mbaezue, Ifenna I.; Zhou, Zhi; Topic, Filip; Tsantrizos, Youla S.
P-Chiral, N-phosphoryl sulfonamide Brønsted acids with an intramolecular hydrogen bond interaction that modulates organocatalysis.
Organic & biomolecular chemistry, 2019, 17, 8690-8694
7157066 CIFC23 H23 N O8 SP -17.6514; 11.634; 13.327
76.022; 79.269; 86.003
1130.68Liu, Yanfei; Wu, Jiaping; Qian, Baiyang; Shang, Yongjia
Controllable construction of isoquinolinedione and isocoumarin scaffolds via Rh<sup>III</sup>-catalyzed C-H annulation of N-tosylbenzamides with diazo compounds.
Organic & biomolecular chemistry, 2019, 17, 8768-8777
7157065 CIFC7 H8 F7 N3 OP 1 21/c 110.986; 9.949; 10.414
90; 98.87; 90
1125Liu, Shulin; Wang, Rui; Zhu, Bo; Guan, Wei; Liang, Fushun
Photo- and dioxygen-enabled radical C(sp<sup>3</sup>)-N(sp<sup>2</sup>) cross-coupling between guanidines and perfluoroalkyl iodides.
Organic & biomolecular chemistry, 2019, 17, 8695-8700
7157064 CIFC9 H12 F7 N3 OP 1 21/n 111.7613; 7.26; 15.9064
90; 101.506; 90
1330.91Liu, Shulin; Wang, Rui; Zhu, Bo; Guan, Wei; Liang, Fushun
Photo- and dioxygen-enabled radical C(sp<sup>3</sup>)-N(sp<sup>2</sup>) cross-coupling between guanidines and perfluoroalkyl iodides.
Organic & biomolecular chemistry, 2019, 17, 8695-8700
7157063 CIFC17 H12 F2 N2 OP 1 21/n 18.94; 10.9431; 14.3252
90; 101.51; 90
1373.27Chen, Guojun; Li, Chenglong; Peng, Jianfeng; Yuan, Zeli; Liu, Peijun; Liu, Xiaozu
Silver-promoted decarboxylative radical addition/annulation of oxamic acids with gem-difluoroolefins: concise access to CF<sub>2</sub>-containing 3,4-dihydroquinolin-2-ones.
Organic & biomolecular chemistry, 2019, 17, 8527-8532
7157062 CIFC23 H20 N2 O2P 1 21/c 19.3497; 9.15478; 21.8715
90; 92.8985; 90
1869.68Chen, Lian-Mei; Zhao, Juan; Xia, An-Jie; Guo, Xiao-Qiang; Gan, Ya; Zhou, Chuang; Yang, Zai-Jun; Yang, Jun; Kang, Tai-Ran
A base-promoted cascade reaction of α,β-unsaturated N-tosylhydrazones with o-hydroxybenzyl alcohols: highly regioselective synthesis of N-sec-alkylpyrazoles.
Organic & biomolecular chemistry, 2019, 17, 8561-8570
7157060 CIFC26 H24 Cl2 N2 O2 SP -18.7442; 11.0021; 14.959
95.314; 106.955; 109.24
1271Wu, Hao; Liu, Yu; He, Ming-Xing; Wen, Hao; Cao, Wei; Chen, Ping; Tang, Yu
Preparation of isoquinazolines via metal-free [4 + 2] cycloaddition of ynamides with nitriles.
Organic & biomolecular chemistry, 2019, 17, 8408-8416
7157059 CIFC25 H28 F2 N4 SP 1 21/c 118.3522; 11.8099; 10.9691
90; 97.346; 90
2357.9Peng, Xiangjun; Qin, Feng; Xu, Mengyue; Zhu, Shaojie; Pan, Yingming; Tang, Haitao; Meng, Xiujin; Wang, Hengshan
Synthesis of imidazo[1,2-c]thiazoles through Pd-catalyzed bicyclization of tert-butyl isonitrile with thioamides.
Organic & biomolecular chemistry, 2019, 17, 8403-8407
7157058 CIFC21 H30 O7P 21 21 217.68291; 12.60214; 21.2697
90; 90; 90
2059.36Chen, Heng-Ye; Liu, Ting-Kai; Yang, Jian; Yang, Xiao-Long
Emerones A-C: three novel merosesquiterpenoids with unprecedented skeletons from Emericella sp. XL029.
Organic & biomolecular chemistry, 2019, 17, 8450-8455
7157057 CIFC22 H32 O8P 21 21 2111.34869; 12.79403; 14.62274
90; 90; 90
2123.16Chen, Heng-Ye; Liu, Ting-Kai; Yang, Jian; Yang, Xiao-Long
Emerones A-C: three novel merosesquiterpenoids with unprecedented skeletons from Emericella sp. XL029.
Organic & biomolecular chemistry, 2019, 17, 8450-8455
7157056 CIFC15 H11 N O2P 1 21/c 110.416; 20.705; 10.7592
90; 98.861; 90
2292.7Pan, Jin-Long; Liu, Tuan-Qing; Chen, Chao; Li, Quan-Zhe; Jiang, Wei; Ding, Tong-Mei; Yan, Zhi-Qiang; Zhu, Guo-Dong
Rhodium(iii)-catalysed cascade [3 + 2] annulation of N-aryloxyacetamides with 3-(hetero)arylpropiolic acids: synthesis of benzofuran-2(3H)-ones.
Organic & biomolecular chemistry, 2019, 17, 8589-8600
7157055 CIFC24 H22 N2 OR -3 :H28.608; 28.608; 11.5472
90; 90; 120
8184.3Xu, Shengbo; Qiao, Shanshan; Sun, Song; Yu, Jin-Tao; Cheng, Jiang
Rhodium-catalyzed C-H activation/annulation of amidines with 4-diazoisochroman-3-imines toward isochromeno[3,4-c]isoquinolines.
Organic & biomolecular chemistry, 2019, 17, 8417-8424
7157054 CIFC33 H30 Br N O6P 1 21/c 18.1114; 35.404; 9.9824
90; 104.195; 90
2779.2Zhang, Wen-Hui; Zhou, Yan-You; He, Xue-Wen; Gong, Yi; Liu, Xiong-Li; Zhou, Ying
An asymmetric iminium ion catalysis-enabled cascade cycloaddition reaction of chromone-oxindole synthons with enals: construction of a spirooxindole-hexahydroxanthone framework.
Organic & biomolecular chemistry, 2019, 17, 8369-8373
7157053 CIFC30 H28 Br N3 O3P -19.7016; 11.8988; 12.2186
65.813; 85.063; 89.505
1281.34Zhang, Chen; Shang, Xinye; Cheng, Yuyu; Li, Fushuai; Zhao, Hanhui; Li, Pengfei; Li, Wenjun
Enantioselective construction of 3-substituted 3-amino-2-oxindoles containing an N,N-ketal skeleton via organocatalyzed aza-addition of isatin imines.
Organic & biomolecular chemistry, 2019, 17, 8374-8378
7157052 CIFC26 H26 Cl N3 O3P 1 21/c 111.1047; 9.546; 22.3027
90; 102.179; 90
2311Zhang, Chen; Shang, Xinye; Cheng, Yuyu; Li, Fushuai; Zhao, Hanhui; Li, Pengfei; Li, Wenjun
Enantioselective construction of 3-substituted 3-amino-2-oxindoles containing an N,N-ketal skeleton via organocatalyzed aza-addition of isatin imines.
Organic & biomolecular chemistry, 2019, 17, 8374-8378
7157051 CIFC23 H24 Br N5 O3C 1 2/c 120.5473; 10.6285; 22.3229
90; 108.475; 90
4623.8Zhang, Chen; Shang, Xinye; Cheng, Yuyu; Li, Fushuai; Zhao, Hanhui; Li, Pengfei; Li, Wenjun
Enantioselective construction of 3-substituted 3-amino-2-oxindoles containing an N,N-ketal skeleton via organocatalyzed aza-addition of isatin imines.
Organic & biomolecular chemistry, 2019, 17, 8374-8378
7157050 CIFC26 H24 Br N5 O3P b c a17.594; 10.7941; 25.355
90; 90; 90
4815.2Zhang, Chen; Shang, Xinye; Cheng, Yuyu; Li, Fushuai; Zhao, Hanhui; Li, Pengfei; Li, Wenjun
Enantioselective construction of 3-substituted 3-amino-2-oxindoles containing an N,N-ketal skeleton via organocatalyzed aza-addition of isatin imines.
Organic & biomolecular chemistry, 2019, 17, 8374-8378
7157049 CIFC22 H22 Br N5 O3P 21 21 2110.238; 10.6914; 19.2761
90; 90; 90
2109.93Zhang, Chen; Shang, Xinye; Cheng, Yuyu; Li, Fushuai; Zhao, Hanhui; Li, Pengfei; Li, Wenjun
Enantioselective construction of 3-substituted 3-amino-2-oxindoles containing an N,N-ketal skeleton via organocatalyzed aza-addition of isatin imines.
Organic & biomolecular chemistry, 2019, 17, 8374-8378
7157048 CIFC18 H14.67 N2 O1.33P -110.755; 14.1162; 15.1222
117.094; 99.24; 90.86
2007.2Pozharskii, Alexander F.; Ozeryanskii, Valery A.; Mikshiev, Vladimir Y.; Chernyshev, Anatoly V.; Metelitsa, Anatoly V.; Antonov, Alexander S.
Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors.
Organic & biomolecular chemistry, 2019, 17, 8221-8233
7157047 CIFC24 H18 N2 OP 1 21/n 121.179; 7.379; 22.305
90; 96.923; 90
3460.4Pozharskii, Alexander F.; Ozeryanskii, Valery A.; Mikshiev, Vladimir Y.; Chernyshev, Anatoly V.; Metelitsa, Anatoly V.; Antonov, Alexander S.
Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors.
Organic & biomolecular chemistry, 2019, 17, 8221-8233
7157046 CIFC18 H16 N2 O2P 1 21/n 14.6952; 20.135; 14.864
90; 93.406; 90
1402.7Pozharskii, Alexander F.; Ozeryanskii, Valery A.; Mikshiev, Vladimir Y.; Chernyshev, Anatoly V.; Metelitsa, Anatoly V.; Antonov, Alexander S.
Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors.
Organic & biomolecular chemistry, 2019, 17, 8221-8233
7157045 CIFC24 H15 N5 O7C 1 2/c 120.993; 16.92; 13.496
90; 119.796; 90
4160Pozharskii, Alexander F.; Ozeryanskii, Valery A.; Mikshiev, Vladimir Y.; Chernyshev, Anatoly V.; Metelitsa, Anatoly V.; Antonov, Alexander S.
Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors.
Organic & biomolecular chemistry, 2019, 17, 8221-8233
7157044 CIFC38 H25 Cl N4 O4P 21 21 217.50014; 16.7058; 22.9329
90; 90; 90
2873.4Pozharskii, Alexander F.; Ozeryanskii, Valery A.; Mikshiev, Vladimir Y.; Chernyshev, Anatoly V.; Metelitsa, Anatoly V.; Antonov, Alexander S.
Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors.
Organic & biomolecular chemistry, 2019, 17, 8221-8233
7157043 CIFC18 H13 Br N2P 1 21/n 17; 10.6452; 18.2521
90; 98.614; 90
1344.74Pozharskii, Alexander F.; Ozeryanskii, Valery A.; Mikshiev, Vladimir Y.; Chernyshev, Anatoly V.; Metelitsa, Anatoly V.; Antonov, Alexander S.
Proton-induced fluorescence in modified quino[7,8-h]quinolines: dual sensing for protons and π-donors.
Organic & biomolecular chemistry, 2019, 17, 8221-8233
7157042 CIFC12 H6 Cl2 N2 O2P 1 21/c 110.4975; 14.8593; 7.2597
90; 101.37; 90
1110.18Sreenivasa Rao, Ramana; Shajan, Femil Joseph; Reddy, D. Srinivasa
A route to access imidazol[1,5-a]indole-1,3-diones and pyrrolo[1,2-c]imidazole-1,3-diones.
Organic & biomolecular chemistry, 2019, 17, 8384-8390
7157041 CIFC22 H19 N5 O2P 1 21/c 114.4652; 15.665; 8.435
90; 91.931; 90
1910.3Gour, Jitendra; Gatadi, Srikanth; Akunuri, Ravikumar; Yaddanapudi, Madhavi Venkata; Nengroo, Mushtaq Ahmad; Datta, Dipak; Chopra, Sidharth; Nanduri, Srinivas
Catalyst-free facile synthesis of polycyclic indole/pyrrole substituted-1,2,3-triazoles.
Organic & biomolecular chemistry, 2019, 17, 8153-8165
7157040 CIFC48 H38 N2 O6P -19.0014; 9.5478; 23.864
91.65; 95.15; 113.925
1862.4Muthusamy, Sengodagounder; Prabu, Ammasi; Suresh, Eringathodi
Copper-catalyzed synthesis of spiro-indolofurobenzopyrans: tandem reactions of diazoamides and O-propargyl salicylaldehydes.
Organic & biomolecular chemistry, 2019, 17, 8088-8093
7157039 CIFC31 H30 O7P -19.539; 9.87; 15.022
95.665; 97.294; 99.247
1374.4Verma, Kamal; Taily, Irshad Maajid; Banerjee, Prabal
Exploitation of donor-acceptor cyclopropanes and N-sulfonyl 1-azadienes towards the synthesis of spiro-cyclopentane benzofuran derivatives.
Organic & biomolecular chemistry, 2019, 17, 8149-8152
7157038 CIFC39 H39 N O9 SP 1 21/c 117.483; 8.483; 24.544
90; 97.103; 90
3612Verma, Kamal; Taily, Irshad Maajid; Banerjee, Prabal
Exploitation of donor-acceptor cyclopropanes and N-sulfonyl 1-azadienes towards the synthesis of spiro-cyclopentane benzofuran derivatives.
Organic & biomolecular chemistry, 2019, 17, 8149-8152
7157037 CIFC31 H45 O6P 21 21 219.97968; 10.81315; 27.7238
90; 90; 90
2991.72Duan, Yulin; Xie, Shuangshuang; Guo, Yi; Qiao, Yuben; Shi, Zhengyi; Tao, Li; Deng, Mengyi; Cao, Yunfang; Xue, Yongbo; Qi, Changxing; Zhang, Yonghui
Przewalcyrones A-F, epoxychromene-containing polycyclic polyprenylated acylphloroglucinols with immunosuppressive activity from Hypericum przewalskii Maxim.
Organic & biomolecular chemistry, 2019, 17, 8234-8242
7157036 CIFC28 H24 N2 OP n a 2113.387; 12.8591; 12.5553
90; 90; 90
2161.3Magyar, Christina L.; Wall, Tyler J.; Davies, Steven B.; Campbell, Molly V.; Barna, Haven A.; Smith, Sydney R.; Savich, Christopher J.; Mosey, R. Adam
Triflic anhydride mediated synthesis of 3,4-dihydroquinazolines: a three-component one-pot tandem procedure.
Organic & biomolecular chemistry, 2019, 17, 7995-8000
7157035 CIFC31 H27 O3 PP 1 21/c 117.0617; 13.611; 11.3034
90; 106.03; 90
2522.9Hou, Hong; Xu, Yue; Yang, Haibo; Yan, Chaoguo; Shi, Yaocheng; Zhu, Shaoqun
Regioselective radical arylation: silver-mediated synthesis of 3-phosphorylated coumarins, quinolin-2(1H)-one and benzophosphole oxides.
Organic & biomolecular chemistry, 2019, 17, 8175-8184
7157034 CIFC31 H28 N O2 PP -110.4035; 10.59; 13.0053
89.785; 77.673; 69.24
1304.9Hou, Hong; Xu, Yue; Yang, Haibo; Yan, Chaoguo; Shi, Yaocheng; Zhu, Shaoqun
Regioselective radical arylation: silver-mediated synthesis of 3-phosphorylated coumarins, quinolin-2(1H)-one and benzophosphole oxides.
Organic & biomolecular chemistry, 2019, 17, 8175-8184
7157033 CIFC29 H24 N O4 PC 1 2/c 122.6531; 11.2558; 20.1149
90; 105.379; 90
4945.2Hou, Hong; Xu, Yue; Yang, Haibo; Yan, Chaoguo; Shi, Yaocheng; Zhu, Shaoqun
Regioselective radical arylation: silver-mediated synthesis of 3-phosphorylated coumarins, quinolin-2(1H)-one and benzophosphole oxides.
Organic & biomolecular chemistry, 2019, 17, 8175-8184
7157032 CIFC47 H45 N O13P 21 21 2111.2462; 16.3107; 25.345
90; 90; 90
4649.1Lu, Kui; Li, Ming; Huang, Yuna; Sun, Yuanyuan; Gong, Zhi; Wei, Qijun; Zhao, Xia; Zhang, Yongmin; Yu, Peng
Total synthesis of wikstrol A and wikstrol B.
Organic & biomolecular chemistry, 2019, 17, 8206-8213
7157031 CIFC30 H37 N O7P 21 21 2110.9844; 12.425; 19.6238
90; 90; 90
2678.28Wang, Wen-Xuan; Cheng, Gui-Guang; Li, Zheng-Hui; Ai, Hong-Lian; He, Juan; Li, Jing; Feng, Tao; Liu, Ji-Kai
Curtachalasins, immunosuppressive agents from the endophytic fungus Xylaria cf. curta.
Organic & biomolecular chemistry, 2019, 17, 7985-7994
7157030 CIFC31 H40 Cl3 N O9P 1 21 18.1478; 12.7979; 15.6927
90; 101.559; 90
1603.17Wang, Wen-Xuan; Cheng, Gui-Guang; Li, Zheng-Hui; Ai, Hong-Lian; He, Juan; Li, Jing; Feng, Tao; Liu, Ji-Kai
Curtachalasins, immunosuppressive agents from the endophytic fungus Xylaria cf. curta.
Organic & biomolecular chemistry, 2019, 17, 7985-7994
7157028 CIFC36 H28 N4 O3P 1 21/n 19.696; 24.284; 12.449
90; 100.612; 90
2881Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157027 CIFC36 H28 Cl N5 O2P -17.9066; 12.8759; 15.1112
93.932; 100.459; 98.838
1487.5Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157026 CIFC37 H31 N5 O3P 1 21 111.932; 7.8696; 16.941
90; 106.606; 90
1524.4Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157025 CIFC35 H28 Br N3 O4P 1 21/n 115.553; 8.7812; 22.8541
90; 106.896; 90
2986.5Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157024 CIFC37 H30 Cl2 F N5 O3C 1 2/c 133.399; 7.9839; 26.148
90; 110.495; 90
6531.1Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157023 CIFC36 H28 Br N5 O2P -17.9473; 12.8859; 15.2264
93.496; 101.326; 98.939
1503.6Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157022 CIFC35 H25 Br Cl N5 O2P -17.9255; 12.9254; 15.224
92.788; 101.518; 99.593
1501.3Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157021 CIFC36 H29 N5 O2P -17.792; 12.8131; 14.7154
96.214; 96.001; 98.326
1434.32Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157020 CIFC36 H27 N3 O3P 1 21/n 19.539; 20.876; 14.712
90; 108.212; 90
2782.9Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157019 CIFC34 H25 N5 O5P 1 21/c 19.5329; 12.0116; 26.3133
90; 92.348; 90
3010.5Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157018 CIFC35 H28 Br N3 O4P 1 21/c 18.8593; 22.333; 15.6805
90; 98.73; 90
3066.5Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157017 CIFC36 H30 Cl2 N4 O3P 1 21/c 111.917; 17.27; 15.382
90; 92.563; 90
3162.6Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157016 CIFC36 H32 N4 O3P -19.5972; 11.9696; 14.6218
104.321; 91.69; 113.084
1482.02Liu, Dan; Sun, Jing; Zhang, Yu; Yan, Chao-Guo
Diastereoselective synthesis of spirocyclic isoxazolo[5,4-c]pyrrolo[2,1-a]isoquinolines via cascade double [3 + 2]cycloadditions.
Organic & biomolecular chemistry, 2019, 17, 8008-8013
7157015 CIFC31 H26 N2 O4 SI 1 2 112.1351; 8.4982; 26.9828
90; 95.024; 90
2772Hajra, Saumen; Bhosale, Suhas Shivajirao; Hazra, Atanu; Kanaujia, Nikhil
The one pot asymmetric synthesis of 3,3'-pyrrolidonyl spiroxindoles via a regio- and stereoselective domino reaction.
Organic & biomolecular chemistry, 2019, 17, 8140-8148
7157014 CIFC48 H69 D2 N O3 Si2P 1 21/c 117.2809; 16.3497; 16.6811
90; 104.161; 90
4569.8Toledo, Hila; Tumanskii, Boris; Sabirov, Denis Sh; Kaushansky, Alexander; Fridman, Natalia; Szpilman, Alex M.
First α-deuterium nitroxides; synthesis and EPR study.
Organic & biomolecular chemistry, 2019, 17, 7900-7906
7157013 CIFC23 H20 Br N O2P 21 21 213.351; 25.715; 5.749
90; 90; 90
1973.8Mondal, Buddhadeb; Balha, Megha; Pan, Subhas Chandra
Organocatalytic asymmetric spirocyclization reactions of cyclic 2,4-dienones with cyanoketones: synthesis of spiro-dihydropyrano cyclohexanones.
Organic & biomolecular chemistry, 2019, 17, 7849-7853
7157012 CIFC80 H80 N2 O4C 1 2/c 125.978; 16.4871; 16.06
90; 94.502; 90
6857.3Wang, Lijiao; Hao, Wei; Han, Yanbing; Shi, Yamei; Li, Shuzhou; Zhang, Chunfang; Xiao, Jinchong
Facile and versatile access to substituted hexabenzoovalene derivatives: characterization and optoelectronic properties.
Organic & biomolecular chemistry, 2019, 17, 7964-7972
7157011 CIFC21 H22 O3P -16.3862; 8.2346; 17.2255
100.358; 97.648; 95.824
875.83Liang, Yi-En; Lu, Chia-Ling; Li, Wen-Tai
Pd-Catalyzed sequential hydroarylation and olefination reactions of 3-allylchromones.
Organic & biomolecular chemistry, 2019, 17, 7569-7583
7157010 CIFC35 H38.32 N4 O0.16 S2P 1 21 18.81055; 20.08758; 9.52368
90; 112.355; 90
1558.85Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157009 CIFC26 H30 N3 O0.5 SC 1 2 114.3834; 10.6941; 29.8026
90; 98.643; 90
4532.1Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157008 CIFC27 H27 N3 S2P 1 21 110.168; 14.93848; 16.29099
90; 99.1361; 90
2443.12Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157007 CIFC35 H38 N4 S2P 19.0135; 9.2173; 10.0939
100.231; 94.54; 112.553
752.08Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157006 CIFC11 H24 N2 SP 43 21 212.9053; 12.9053; 16.087
90; 90; 90
2679.24Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157005 CIFC28 H32 N2 SP 21 21 219.6029; 10.57062; 23.0787
90; 90; 90
2342.69Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157004 CIFC25 H28 N2 SP 43 21 28.73671; 8.73671; 56.4484
90; 90; 90
4308.71Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157003 CIFC46 H44 N4 S2P 1 21 19.16773; 14.33308; 15.08193
90; 104.093; 90
1922.15Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157002 CIFC28 H37 N3 O2 SC 2 2 2111.09166; 13.89141; 34.8221
90; 90; 90
5365.35Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157001 CIFC26 H30 N2 SP 1 21 117.6143; 8.8624; 29.0155
90; 98.484; 90
4479.9Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7157000 CIFC24 H26 N2 SC 1 2 111.1159; 13.1734; 28.2695
90; 96.402; 90
4113.81Prusinowska, Natalia; Czapik, Agnieszka; Wojciechowska, Martika; Kwit, Marcin
Dynamic optical activity induction in the N-alkyl-N'-trityl ureas and thioureas.
Organic & biomolecular chemistry, 2019, 17, 7782-7793
7156999 CIFC30 H44 Cu2 N2 O8P 1 21/c 116.608; 11.434; 16.771
90; 100.803; 90
3128.3Kirillova, Marina V.; Fernandes, Tiago A.; André, Vânia; Kirillov, Alexander M.
Mild C-H functionalization of alkanes catalyzed by bioinspired copper(ii) cores.
Organic & biomolecular chemistry, 2019, 17, 7706-7714
7156998 CIFC23 H31 Cu N O6P 1 21/c 110.6013; 25.155; 8.9311
90; 109.342; 90
2247.3Kirillova, Marina V.; Fernandes, Tiago A.; André, Vânia; Kirillov, Alexander M.
Mild C-H functionalization of alkanes catalyzed by bioinspired copper(ii) cores.
Organic & biomolecular chemistry, 2019, 17, 7706-7714
7156997 CIFC15 H28 Cu0.5 N O7P 1 21/n 110.1856; 16.187; 11.0278
90; 91.519; 90
1817.6Kirillova, Marina V.; Fernandes, Tiago A.; André, Vânia; Kirillov, Alexander M.
Mild C-H functionalization of alkanes catalyzed by bioinspired copper(ii) cores.
Organic & biomolecular chemistry, 2019, 17, 7706-7714
7156996 CIFC20 H18 N2 O4 SP -19.231; 9.999; 11.902
113.249; 91.355; 107.746
948.2Tian, Ting; Dong, An-Shun; Chen, Dan; Cao, Xian-Ting; Wang, Guannan
Regioselective C-C cross-coupling of 1,2,4-thiadiazoles with maleimides through iridium-catalyzed C-H activation.
Organic & biomolecular chemistry, 2019, 17, 7664-7668
7156995 CIFC18 H16 Br2 N2 O3P -15.574; 12.623; 14.179
110.91; 95.03; 95.13
920.5Sun, Li; Liu, Yi; Wang, Yankai; Li, Yuanyuan; Liu, Zhiwen; Lu, Tao; Li, Wenhai
An efficient synthesis of oxazolines via a cascade reaction between azaoxyallyl cations and 1,2-benzisoxazoles.
Organic & biomolecular chemistry, 2019, 17, 7526-7530
7156994 CIFC15 H12 Cl3 N3P n m a10.485; 6.832; 21.082
90; 90; 90
1510.2Jiang, Shaohua; Yang, Zhihai; Guo, Ziyin; Li, Yibiao; Chen, Lu; Zhu, Zhongzhi; Chen, Xiuwen
Transition metal-free α-methylation of 1,8-naphthyridine derivatives using DMSO as methylation reagent.
Organic & biomolecular chemistry, 2019, 17, 7416-7424
7156993 CIFC35 H31 Br N2 O4 SP 21 21 217.2208; 16.3286; 27.1076
90; 90; 90
3196.1Franc, Michael; Urban, Michal; Císařová, Ivana; Veselý, Jan
Highly enantioselective addition of sulfur-containing heterocycles to isatin-derived ketimines.
Organic & biomolecular chemistry, 2019, 17, 7309-7314
7156992 CIFC25 H19 Br2 N3 O5P 1 21/c 111.2334; 9.4327; 23.5205
90; 92; 90
2490.7Hajra, Saumen; Maity, Subrata; Roy, Sayan; Das, Dhiraj
Controlling the regioselectivity of the ring opening of spiro-epoxyoxindoles for efficient synthesis of C(3)-N(1')-bisindoles and C(3)-N(1')-diindolylmethane.
Organic & biomolecular chemistry, 2019, 17, 7747-7759
7156991 CIFC31 H33 N3 O4P -19.899; 11.547; 13.186
111.235; 91.111; 102.013
1366.7Hajra, Saumen; Maity, Subrata; Roy, Sayan; Das, Dhiraj
Controlling the regioselectivity of the ring opening of spiro-epoxyoxindoles for efficient synthesis of C(3)-N(1')-bisindoles and C(3)-N(1')-diindolylmethane.
Organic & biomolecular chemistry, 2019, 17, 7747-7759
7156990 CIFC18 H21 N O4P 1 21/n 117.209; 5.034; 19.434
90; 104.812; 90
1627.6Mohr, Lisa-Marie; Bauer, Andreas; Jandl, Christian; Bach, Thorsten
Visible light-mediated intermolecular [2 + 2] photocycloaddition of 1-aryl-2-nitroethenes and olefins.
Organic & biomolecular chemistry, 2019, 17, 7192-7203
7156989 CIFC25 H17 N O3P 1 21/n 113.455; 10.3927; 13.4329
90; 95.302; 90
1870.3Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Ruthenium(ii)-catalysed selective C(sp<sup>2</sup>)-H bond benzoxylation of biologically appealing N-arylisoindolinones.
Organic & biomolecular chemistry, 2019, 17, 7517-7525
7156988 CIFC21 H14 N2 O5P 1 21/c 110.9939; 10.325; 15.434
90; 98.239; 90
1733.9Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Ruthenium(ii)-catalysed selective C(sp<sup>2</sup>)-H bond benzoxylation of biologically appealing N-arylisoindolinones.
Organic & biomolecular chemistry, 2019, 17, 7517-7525
7156987 CIFC22 H17 N O4P -111.7123; 11.9264; 14.137
88.483; 70.167; 75.429
1794.1Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Ruthenium(ii)-catalysed selective C(sp<sup>2</sup>)-H bond benzoxylation of biologically appealing N-arylisoindolinones.
Organic & biomolecular chemistry, 2019, 17, 7517-7525
7156986 CIFC22 H17 N O3P 1 21/c 18.6965; 10.6905; 18.5537
90; 96.339; 90
1714.4Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Ruthenium(ii)-catalysed selective C(sp<sup>2</sup>)-H bond benzoxylation of biologically appealing N-arylisoindolinones.
Organic & biomolecular chemistry, 2019, 17, 7517-7525
7156985 CIFC21 H15 N O3C 1 2/c 116.076; 8.828; 11.834
90; 103.487; 90
1633.2Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Ruthenium(ii)-catalysed selective C(sp<sup>2</sup>)-H bond benzoxylation of biologically appealing N-arylisoindolinones.
Organic & biomolecular chemistry, 2019, 17, 7517-7525
7156984 CIFC20 H20 N4P 1 21/n 19.0962; 10.1454; 18.0969
90; 92.369; 90
1668.64Shiva Kumar, K.; Naikawadi, Praveen Kumar; Jatoth, Ramanna; Dandela, Rambabu
Bimetallic Cu/Pd-catalyzed three-component azide-alkyne cycloaddition/isocyanide insertion: synthesis of fully decorated tricyclic triazoles.
Organic & biomolecular chemistry, 2019, 17, 7320-7324
7156983 CIFC20 H20 N4 OP -19.1911; 10.2029; 10.5844
105.786; 112.987; 97.227
848.6Shiva Kumar, K.; Naikawadi, Praveen Kumar; Jatoth, Ramanna; Dandela, Rambabu
Bimetallic Cu/Pd-catalyzed three-component azide-alkyne cycloaddition/isocyanide insertion: synthesis of fully decorated tricyclic triazoles.
Organic & biomolecular chemistry, 2019, 17, 7320-7324
7156982 CIFC42 H43.25 B F2 N5 O8 SP -18.04807; 20.9106; 25.9109
109.598; 95.323; 99.3812
4001.7Sirbu, D.; Zeng, L.; Waddell, P. G.; Benniston, A. C.
An unprecedented oxidised julolidine-BODIPY conjugate and its application in real-time ratiometric fluorescence sensing of sulfite.
Organic & biomolecular chemistry, 2019, 17, 7360-7368
7156981 CIFC27 H29 O4 PP 21 21 216.0344; 31.7014; 12.0302
90; 90; 90
2301.36Salin, Alexey V.; Islamov, Daut R.
Phosphine-catalyzed Michael additions to α-methylene-γ-butyrolactones.
Organic & biomolecular chemistry, 2019, 17, 7293-7299
7156980 CIFC17 H24 O8P 1 21/c 110.1251; 10.1582; 17.4602
90; 95.237; 90
1788.3Salin, Alexey V.; Islamov, Daut R.
Phosphine-catalyzed Michael additions to α-methylene-γ-butyrolactones.
Organic & biomolecular chemistry, 2019, 17, 7293-7299
7156979 CIFC17 H17 O3 PP b c a8.8852; 10.6649; 31.4503
90; 90; 90
2980.22Salin, Alexey V.; Islamov, Daut R.
Phosphine-catalyzed Michael additions to α-methylene-γ-butyrolactones.
Organic & biomolecular chemistry, 2019, 17, 7293-7299
7156978 CIFC37 H48 O10P 21 21 219.751; 16.7972; 20.8431
90; 90; 90
3413.9Salin, Alexey V.; Islamov, Daut R.
Phosphine-catalyzed Michael additions to α-methylene-γ-butyrolactones.
Organic & biomolecular chemistry, 2019, 17, 7293-7299
7156977 CIFC24 H22 O6P 1 21/n 18.8734; 16.0071; 14.189
90; 100.72; 90
1980.2Han, Wenyong; Yang, Yihui; Zhu, Yingguang; Shi, Yian
A facile copper(i)-catalyzed homo-coupling of indanone derivatives using diaziridinone under mild conditions.
Organic & biomolecular chemistry, 2019, 17, 6998-7001
7156976 CIFC23 H20 Cl2 O6C 1 2/c 112.9425; 15.6165; 10.6618
90; 101.551; 90
2111.3Han, Wenyong; Yang, Yihui; Zhu, Yingguang; Shi, Yian
A facile copper(i)-catalyzed homo-coupling of indanone derivatives using diaziridinone under mild conditions.
Organic & biomolecular chemistry, 2019, 17, 6998-7001
7156975 CIFC30 H28 N2 O4P 21 21 218.5232; 13.562; 21.283
90; 90; 90
2460.1Shahrestani, Naeimeh; Khosravi, Hormoz; Jadidi, Khosrow; Notash, Behrouz; Naderi, Soheila
Organocatalytic synthesis of enantiopure spiro acenaphthyl-pyrrolizidine/pyrrolidines: justifying the regioselectivity based on a distortion/interaction model.
Organic & biomolecular chemistry, 2019, 17, 7013-7024
7156974 CIFC28 H26 N2 O4P 21 21 218.1876; 14.121; 19.915
90; 90; 90
2302.5Shahrestani, Naeimeh; Khosravi, Hormoz; Jadidi, Khosrow; Notash, Behrouz; Naderi, Soheila
Organocatalytic synthesis of enantiopure spiro acenaphthyl-pyrrolizidine/pyrrolidines: justifying the regioselectivity based on a distortion/interaction model.
Organic & biomolecular chemistry, 2019, 17, 7013-7024
7156973 CIFC23 H23 N O6P 21 21 218.7557; 14.297; 16.454
90; 90; 90
2059.7Shahrestani, Naeimeh; Khosravi, Hormoz; Jadidi, Khosrow; Notash, Behrouz; Naderi, Soheila
Organocatalytic synthesis of enantiopure spiro acenaphthyl-pyrrolizidine/pyrrolidines: justifying the regioselectivity based on a distortion/interaction model.
Organic & biomolecular chemistry, 2019, 17, 7013-7024
7156972 CIFC17 H12 N2 O2P 21 21 218.2455; 11.3533; 13.652
90; 90; 90
1278Ahire, Milind M.; Pol, Mahesh D.; Kavale, Dattatry S.; Gonnade, Rajesh G.; Mhaske, Santosh B.
Stereoselective construction of deoxy-cruciferane alkaloids by NHC-catalyzed intramolecular annulation of homoenolate with quinazolinone.
Organic & biomolecular chemistry, 2019, 17, 7135-7139

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