Crystallography Open Database

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7157626 CIFC37 H39 F3 N8 O13P 1 21 112.9906; 11.1438; 14.8377
90; 103.257; 90		2090.73He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157627 CIFC17 H22 N6 O11P 1 21 17.7778; 13.2995; 11.4128
90; 91.458; 90		1180.17He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157628 CIFC20 H27 N7 O12P 1 21 19.6273; 8.8714; 16.549
90; 101.469; 90		1385.2He, Huan; Cao, Ruiyuan; Cao, Ruidi; Liu, Xiao-Yu; Li, Wei; Yu, Di; Li, Yuexiang; Liu, Miaomiao; Wu, Yanmei; Wu, Pingzhou; Yang, Jin-Song; Yan, Yunzheng; Yang, Jingjing; Zheng, Zhi-Bing; Zhong, Wu; Qin, Yong
A light- and heat-driven glycal diazidation approach to nitrogenous carbohydrate derivatives with antiviral activity.
Organic & biomolecular chemistry, 2020, 18, 6155-6161
7157629 CIFC11 H11 N O2P 21 21 217.5291; 7.4902; 17.0281
90; 90; 90		960.29Braire, Julien; Dorcet, Vincent; Vidal, Joëlle; Lalli, Claudia; Carreaux, François
BINOL derivatives-catalysed enantioselective allylboration of isatins: application to the synthesis of (R)-chimonamidine.
Organic & biomolecular chemistry, 2020, 18, 6042-6046
7157630 CIFC12 H13 N O2P 21 21 217.3607; 8.0406; 17.598
90; 90; 90		1041.5Braire, Julien; Dorcet, Vincent; Vidal, Joëlle; Lalli, Claudia; Carreaux, François
BINOL derivatives-catalysed enantioselective allylboration of isatins: application to the synthesis of (R)-chimonamidine.
Organic & biomolecular chemistry, 2020, 18, 6042-6046
7157631 CIFC24 H17.19 N3 O1.1P 1 21/n 110.5627; 8.8564; 19.8868
90; 98.7088; 90		1838.91Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157632 CIFC15 H14 N2 O2P 1 21/c 119.1254; 5.4936; 11.5714
90; 98.8783; 90		1201.21Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157633 CIFC24.25 H14.5 Br3 Cl0.5 N3 OC 1 2/c 126.7209; 15.6427; 11.8698
90; 104.361; 90		4806.38Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157634 CIFC27 H23 N3 OP -110.4157; 10.5063; 11.3815
112.529; 108.753; 99.9684		1024.96Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157635 CIFC9 H9 N O2P 1 n 114.1319; 3.8682; 15.5153
90; 110.946; 90		792.1Cheng, Li-Ting; Luo, Sheng-Qi; Hong, Bor-Cherng; Chen, Chia-Ling; Li, Wen-Shan; Lee, Gene-Hsiang
Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities.
Organic & biomolecular chemistry, 2020, 18, 6247-6252
7157636 CIFC17 H28 O4P 1 21/c 115.2304; 9.1246; 22.238
90; 95.627; 90		3075.6Kobayashi, Toyoharu; Tomita, Yui; Kawamoto, Yuichiro; Ito, Hisanaka
Highly stereocontrolled total synthesis of secodolastane diterpenoid isolinearol.
Organic & biomolecular chemistry, 2020, 18, 7316-7320
7157637 CIFC20 H32 O4P 1 21/c 110.559; 8.9149; 19.341
90; 92.146; 90		1819.3Kobayashi, Toyoharu; Tomita, Yui; Kawamoto, Yuichiro; Ito, Hisanaka
Highly stereocontrolled total synthesis of secodolastane diterpenoid isolinearol.
Organic & biomolecular chemistry, 2020, 18, 7316-7320
7157638 CIFC28 H30 N2 O3 S4P 21 21 219.4421; 14.8451; 19.2118
90; 90; 90		2692.9García de la Concepción, Juan; Ávalos, Martín; Jiménez, José L; Cintas, Pedro; Light, Mark E.
A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen.
Organic & biomolecular chemistry, 2020, 18, 6328-6339
7157639 CIFC22 H18 N2 O3 S4R -3 :H23.7837; 23.7837; 21.6038
90; 90; 120		10583.3García de la Concepción, Juan; Ávalos, Martín; Jiménez, José L; Cintas, Pedro; Light, Mark E.
A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen.
Organic & biomolecular chemistry, 2020, 18, 6328-6339
7157640 CIFC34 H26 N2 O3 S4P 21 21 2112.482; 12.8583; 19.5132
90; 90; 90		3131.82García de la Concepción, Juan; Ávalos, Martín; Jiménez, José L; Cintas, Pedro; Light, Mark E.
A fully diastereoselective oxidation of a mesoionic dipole with triplet molecular oxygen.
Organic & biomolecular chemistry, 2020, 18, 6328-6339
7157641 CIFC16 H12 Br N3P 1 21/n 17.1264; 19.867; 19.419
90; 94.326; 90		2741.5Chatterjee, Arpita; Murmu, Chudamani; Peruncheralathan, S.
Copper-catalysed <i>N</i>-arylation of 5-aminopyrazoles: a simple route to pyrazolo[3,4-<i>b</i>]indoles.
Organic & biomolecular chemistry, 2020, 18, 6571-6581
7157642 CIFC36.5 H28 Cl2 O4F d d 259.6625; 17.3644; 11.0242
90; 90; 90		11421.1Tanaka, Kenta; Asada, Yosuke; Hoshino, Yujiro; Honda, Kiyoshi
Visible-light-induced [4 + 2] cycloaddition of pentafulvenes by organic photoredox catalysis.
Organic & biomolecular chemistry, 2020, 18, 8074-8078
7157643 CIFC33 H24 Cl2 O4P 1 21/c 115.2283; 9.8746; 18.4264
90; 110.126; 90		2601.65Tanaka, Kenta; Asada, Yosuke; Hoshino, Yujiro; Honda, Kiyoshi
Visible-light-induced [4 + 2] cycloaddition of pentafulvenes by organic photoredox catalysis.
Organic & biomolecular chemistry, 2020, 18, 8074-8078
7157644 CIFC21 H16 N2 O4P b c n17.6367; 13.5661; 14.5573
90; 90; 90		3483Sharma, Suraj; Dutta, Nibedita Baruah; Bhuyan, Mayurakhi; Das, Babulal; Baishya, Gakul
<i>tert</i>-Butylhydroperoxide (TBHP) mediated oxidative cross-dehydrogenative coupling of quinoxalin-2(1<i>H</i>)-ones with 4-hydroxycoumarins, 4-hydroxy-6-methyl-2-pyrone and 2-hydroxy-1,4-naphthoquinone under metal-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6537-6548
7157645 CIFC24 H32 N4 O8P c a 219.621; 8.003; 33.196
90; 90; 90		2556Taily, Irshad Maajid; Saha, Debarshi; Banerjee, Prabal
Palladium-catalyzed regio- and stereoselective access to allyl ureas/carbamates: facile synthesis of imidazolidinones and oxazepinones.
Organic & biomolecular chemistry, 2020, 18, 6564-6570
7157646 CIFC26 H27 Br N2 O5P 1 21/c 18.0617; 26.398; 11.8969
90; 91.684; 90		2530.7Taily, Irshad Maajid; Saha, Debarshi; Banerjee, Prabal
Palladium-catalyzed regio- and stereoselective access to allyl ureas/carbamates: facile synthesis of imidazolidinones and oxazepinones.
Organic & biomolecular chemistry, 2020, 18, 6564-6570
7157647 CIFC19 H17 Br N2 O2P 1 21/c 110.495; 21.897; 7.842
90; 96.57; 90		1790.3Ma, Liyao; Ou, Pengcheng; Huang, Xueliang
Divergent synthesis of 1,3,5-tri and 1,3-disubstituted pyrazoles under transition metal-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6487-6491
7157648 CIFC20 H15 N O3P b c a13.5094; 11.092; 21.2668
90; 90; 90		3186.8Yang, Fazhou; Liu, Ziyan; Liu, Hao; Shangguan, Yu; Deng, Hao; Huang, Jiaxing; Xiao, Yumei; Guo, Hongchao; Zhang, Cheng
Cu-Catalysed synthesis of benzo[f]indole-2,4,9(3H)-triones by the reaction of 2-amino-1,4-napthoquinones with α-bromocarboxylates.
Organic & biomolecular chemistry, 2020, 18, 6724-6731
7157649 CIFC19 H23 Cl2 N3 O4 S2P n m a15.0501; 23.9887; 6.1915
90; 90; 90		2235.33Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157650 CIFC19 H23 F2 N3 O4 S2P 1 21/c 115.0587; 11.9394; 11.6556
90; 90.844; 90		2095.4Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157651 CIFC20 H23 Cl5 D N3 O4 S2P 21 21 2110.5857; 14.0014; 17.5197
90; 90; 90		2596.68Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157652 CIFC19 H23 Cl2 N3 O4 S2P n m a15.0515; 23.4696; 6.1833
90; 90; 90		2184.27Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157653 CIFC19 H23 Br2 N3 O4 S2P n m a15.1555; 24.3132; 6.1544
90; 90; 90		2267.77Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157654 CIFC20 H23 Cl3 D F2 N3 O4 S2P 21 21 2110.4481; 14.3121; 16.4591
90; 90; 90		2461.2Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157655 CIFC19 H23 I2 N3 O4 S2P n m a15.4374; 24.9622; 6.1336
90; 90; 90		2363.59Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157656 CIFC19 H23 I2 N3 O4 S2P n m a15.4193; 24.5788; 6.1039
90; 90; 90		2313.3Kletskov, Alexey V.; Zatykina, Anastasya D.; Grudova, Mariya V.; Sinelshchikova, Anna A.; Grigoriev, Mikhail S.; Zaytsev, Vladimir P.; Gil, Diego M.; Novikov, Roman A.; Zubkov, Fedor I.; Frontera, Antonio
Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.
Organic & biomolecular chemistry, 2020, 18, 8386-8394
7157657 CIFC28 H32 O8I -431.5358; 31.5358; 5.2684
90; 90; 90		5239.5Gadigennavar, Savita; Sankararaman, Sethuraman
Synthesis and application of 3,4,7,8-tetrakis-exo-methylenecycloocta-1,5-diene as a versatile Diels-Alder diene: synthesis of V-shaped cyclooctatetraene fused acenes.
Organic & biomolecular chemistry, 2020, 18, 6738-6744
7157658 CIFC68 H62 N4 O13F d d 221.741; 13.765; 21.012
90; 90; 90		6288.2Gadigennavar, Savita; Sankararaman, Sethuraman
Synthesis and application of 3,4,7,8-tetrakis-exo-methylenecycloocta-1,5-diene as a versatile Diels-Alder diene: synthesis of V-shaped cyclooctatetraene fused acenes.
Organic & biomolecular chemistry, 2020, 18, 6738-6744
7157659 CIFC32 H26 N2 O4P 1 21/c 113.8872; 9.9072; 19.4383
90; 90.026; 90		2674.38Gadigennavar, Savita; Sankararaman, Sethuraman
Synthesis and application of 3,4,7,8-tetrakis-exo-methylenecycloocta-1,5-diene as a versatile Diels-Alder diene: synthesis of V-shaped cyclooctatetraene fused acenes.
Organic & biomolecular chemistry, 2020, 18, 6738-6744
7157660 CIFC15 H13 N O3P 1 21/c 17.0483; 9.642; 17.816
90; 93.573; 90		1208.42Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157661 CIFC14 H11 N O3P 1 21/c 111.1412; 8.63104; 12.612
90; 98.0678; 90		1200.77Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157662 CIFC14 H17 N O6C 1 2/c 123.1618; 6.1459; 20.0176
90; 95.672; 90		2835.56Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157663 CIFC20 H25 N3 O3P 1 21/c 113.962; 8.28868; 17.5984
90; 112.379; 90		1883.22Greve, Eric; Lindeman, Sergey V.; Scartelli, Christina; Lin, Lin; Flaumenhaft, Robert; Dockendorff, Chris
Route exploration and synthesis of the reported pyridone-based PDI inhibitor STK076545.
Organic & biomolecular chemistry, 2020, 18, 6665-6681
7157664 CIFC17 H21 N3P -16.7441; 9.9379; 12.0364
69.995; 75.972; 81.277		733.33Aksenov, Nicolai A.; Aksenov, Alexander V.; Kirilov, Nikita K.; Arutiunov, Nikolai A.; Aksenov, Dmitrii A.; Maslivetc, Vladimir; Zhao, Zhenze; Du, Liqin; Rubin, Michael; Kornienko, Alexander
Nitroalkanes as electrophiles: synthesis of triazole-fused heterocycles with neuroblastoma differentiation activity.
Organic & biomolecular chemistry, 2020, 18, 6651-6664
7157665 CIFC11 H9 N3P 1 21/c 19.1934; 10.6902; 18.2767
90; 100.449; 90		1766.43Aksenov, Nicolai A.; Aksenov, Alexander V.; Kirilov, Nikita K.; Arutiunov, Nikolai A.; Aksenov, Dmitrii A.; Maslivetc, Vladimir; Zhao, Zhenze; Du, Liqin; Rubin, Michael; Kornienko, Alexander
Nitroalkanes as electrophiles: synthesis of triazole-fused heterocycles with neuroblastoma differentiation activity.
Organic & biomolecular chemistry, 2020, 18, 6651-6664
7157666 CIFC134 H130 Cl6 F6 N18 O19C 2 2 2135.445; 36.434; 45.806
90; 90; 90		59154Yang, Ling; Ma, Chunmiao; Kauffmann, Brice; Li, Dongyao; Gan, Quan
Absolute handedness control of oligoamide double helices by chiral oxazolylaniline induction.
Organic & biomolecular chemistry, 2020, 18, 6643-6650
7157667 CIFC15 H30 O S2P 21 21 215.0392; 8.4897; 38.3953
90; 90; 90		1642.6Scheutz, Georg M.; Rowell, Jonathan L.; Wang, Fu-Sheng; Abboud, Khalil A.; Peng, Chi-How; Sumerlin, Brent S.
Synthesis of functional 1,2-dithiolanes from 1,3-bis-<i>tert</i>-butyl thioethers.
Organic & biomolecular chemistry, 2020, 18, 6509-6513
7157668 CIFC5 H9 O S2I 41/a :219.7501; 19.7501; 7.4965
90; 90; 90		2924.1Scheutz, Georg M.; Rowell, Jonathan L.; Wang, Fu-Sheng; Abboud, Khalil A.; Peng, Chi-How; Sumerlin, Brent S.
Synthesis of functional 1,2-dithiolanes from 1,3-bis-<i>tert</i>-butyl thioethers.
Organic & biomolecular chemistry, 2020, 18, 6509-6513
7157669 CIFC20 H18 N6P 1 21/c 15.866; 8.1481; 18.3926
90; 90; 90		879.11Rahman, Iftakur; Deka, Bhaskar; Thakuria, Ranjit; Deb, Mohit L.; Baruah, Pranjal K.
L-Proline-catalyzed regioselective C1 arylation of tetrahydroisoquinolines through a multicomponent reaction under solvent-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6514-6518
7157670 CIFC27 H28 N4P 1 21/c 113.786; 13.94; 12.043
90; 95.844; 90		2302.4Rahman, Iftakur; Deka, Bhaskar; Thakuria, Ranjit; Deb, Mohit L.; Baruah, Pranjal K.
L-Proline-catalyzed regioselective C1 arylation of tetrahydroisoquinolines through a multicomponent reaction under solvent-free conditions.
Organic & biomolecular chemistry, 2020, 18, 6514-6518
7157671 CIFC26 H25 N5 O12P -110.0331; 11.8988; 13.4124
108; 99.413; 106.679		1401.73Luo, Yan-Long; Liu, Yu-Feng; Guan, Bing-Tao
Alkyl lithium-catalyzed benzylic C-H bond addition of alkyl pyridines to α-alkenes.
Organic & biomolecular chemistry, 2020, 18, 6622-6626
7157672 CIFC35 H32 Br Cl3 N2 O3 SP -19.5464; 11.3522; 16.3209
79.8713; 82.8439; 76.7777		1688.44Rapelli, Chandrashekhar; Sridhar, Balasubramanian; Subba Reddy, B. V.
Tandem Prins cyclization for the synthesis of indole fused spiro-1,4-diazocane scaffolds.
Organic & biomolecular chemistry, 2020, 18, 6710-6715
7157673 CIFC20 H16 N2 O SP 1 21/n 111.05; 14.7669; 11.3282
90; 109.477; 90		1742.69Song, Xiaoxiao; Xu, Lei; Ni, Qijian
Highly diastereoselective synthesis of 3-methylenetetrahydropyrans by palladium-catalyzed oxa-[4 + 2] cycloaddition of 2-alkenylbenzothiazoles.
Organic & biomolecular chemistry, 2020, 18, 6617-6621
7157674 CIFC31 H34 Br N O4P 1 21/c 110.805; 28.766; 9.1158
90; 98.138; 90		2804.8Wang, Ziyang; Huang, Anqi; Fang, Fang; Li, Pengfei; Liu, Guokai; Li, Wenjun
Non-hydrogen bond catalyst-mediated diastereoselective conjugate additions of 5H-oxazol-4-ones to o-hydroxyphenyl-substituted p-quinone methides.
Organic & biomolecular chemistry, 2020, 18, 6807-6811
7157675 CIFC34 H25 N O4P 21 21 217.2273; 12.6042; 29.1348
90; 90; 90		2654.02Mu, Yuanyang; Yuan, Yang; Wang, Ye; Xu, Murong; Feng, Ye; Zhao, Yulei; Li, Yanzhong
Synthesis of indoline-fused eight-membered azaheterocycles through Zn-catalyzed dearomatization of indoles and subsequent base-promoted C-C activation.
Organic & biomolecular chemistry, 2020, 18, 6916-6926
7157676 CIFC34 H24 Br N O4P 1 21/c 111.571; 17.156; 13.431
90; 91.359; 90		2665.5Mu, Yuanyang; Yuan, Yang; Wang, Ye; Xu, Murong; Feng, Ye; Zhao, Yulei; Li, Yanzhong
Synthesis of indoline-fused eight-membered azaheterocycles through Zn-catalyzed dearomatization of indoles and subsequent base-promoted C-C activation.
Organic & biomolecular chemistry, 2020, 18, 6916-6926
7157677 CIFC27 H27 Br N8 O5 SP 1 21/n 19.7202; 11.6843; 24.726
90; 93.705; 90		2802.4Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157678 CIFC27.5 H31 F N7 O4 SP -113.4741; 13.4934; 15.7758
84.2195; 85.3686; 76.9008		2774.41Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157679 CIFC25 H25 N7 O3 SP b c a9.7574; 16.3229; 33.1283
90; 90; 90		5276.3Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157680 CIFC27 H32 F N7 O5 SP 1 21/c 117.9516; 16.7643; 19.6754
90; 112.959; 90		5452.2Izmest'ev, Alexei N.; Gazieva, Galina A.; Karnoukhova, Valentina A.; Kravchenko, Angelina N.
Diastereodivergent synthesis of dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties.
Organic & biomolecular chemistry, 2020, 18, 6905-6911
7157681 CIFC21 H21 N O3P -19.6969; 11.4348; 24.2698
85.022; 85.218; 82.945		2653.4Schendera, Eva; Villinger, Alexander; Brasholz, Malte
Photoinduced iodine-mediated tandem dehydrogenative Povarov cyclisation/C-H oxygenation reactions.
Organic & biomolecular chemistry, 2020, 18, 6912-6915
7157682 CIFC15 H18 N4 O7P 1 21 14.7625; 13.0451; 13.8262
90; 95.126; 90		855.55Nathanael, Joses G.; White, Jonathan M.; Richter, Annika; Nuske, Madison R.; Wille, Uta
Oxidative damage of proline residues by nitrate radicals (NO<sub>3</sub>˙): a kinetic and product study.
Organic & biomolecular chemistry, 2020, 18, 6949-6957
7157683 CIFC23 H17 Cl F3 NP -18.6636; 8.9777; 13.8142
83.784; 78.625; 68.828		981.4Li, Peng-Hua; Wei, Yin; Shi, Min
Cu(I)-Catalyzed addition-cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs).
Organic & biomolecular chemistry, 2020, 18, 7127-7138
7157684 CIFC27 H26 F3 NP -18.754; 13.9202; 20.4884
70.805; 84.483; 81.586		2329.4Li, Peng-Hua; Wei, Yin; Shi, Min
Cu(I)-Catalyzed addition-cycloisomerization difunctionalization reaction of 1,3-enyne-alkylidenecyclopropanes (ACPs).
Organic & biomolecular chemistry, 2020, 18, 7127-7138
7157685 CIFC24 H19 N3P 1 21/c 118.4957; 7.8032; 25.76
90; 92.571; 90		3714.1Yang, Jianhua; Xiong, Shaoqi; Ren, Yongsheng; Xiao, Tiebo; Jiang, Yubo
Copper-catalyzed cross-coupling and sequential allene-mediated cyclization for the synthesis of 1,2,3-triazolo[1,5-<i>a</i>]quinolines.
Organic & biomolecular chemistry, 2020, 18, 7174-7182
7157686 CIFC22 H24 F3 N O2P 1 21/c 118.7943; 11.2236; 9.8308
90; 95.655; 90		2063.6Ma, Rui-Jun; Sun, Jian-Ting; Liu, Chang-Hong; Chen, Ling; Si, Chang-Mei; Wei, Bang-Guo
Synthesis of 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline through nucleophilic addition of organozinc reagents to <i>N</i>,<i>O</i>-acetals.
Organic & biomolecular chemistry, 2020, 18, 7139-7150
7157687 CIFC16 H15 N O3P c c n14.3884; 26.944; 6.9828
90; 90; 90		2707.1Borgohain, Hemi; Talukdar, Kangkan; Sarma, Bipul; Das, Sajal Kumar
Regioselectivity of the trifluoroethanol-promoted intramolecular <i>N</i>-Boc-epoxide cyclization towards 1,3-oxazolidin-2-ones and 1,3-oxazinan-2-ones.
Organic & biomolecular chemistry, 2020, 18, 7401-7413
7157688 CIFC16 H15 N O3P -17.313; 9.4042; 9.8866
97.32; 95.213; 94.533		668.77Borgohain, Hemi; Talukdar, Kangkan; Sarma, Bipul; Das, Sajal Kumar
Regioselectivity of the trifluoroethanol-promoted intramolecular <i>N</i>-Boc-epoxide cyclization towards 1,3-oxazolidin-2-ones and 1,3-oxazinan-2-ones.
Organic & biomolecular chemistry, 2020, 18, 7401-7413
7157689 CIFC21 H16 N2 OP b c a14.6384; 6.909; 30.7229
90; 90; 90		3107.21Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157690 CIFC20 H12 F N2P 1 21/n 110.3439; 6.8286; 20.1913
90; 97.86; 90		1412.8Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157691 CIFC20 H13 F N2P -16.0455; 11.0023; 11.7294
112.103; 96.044; 93.256		714.87Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157692 CIFC20 H12 F2 N2P -17.8602; 8.983; 11.3189
94.775; 108.443; 100.754		736.11Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157693 CIFC22 H18 N2 O2P -15.9542; 10.6468; 13.6281
83.162; 86.529; 76.857		834.81Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157694 CIFC23 H20 N2 O3P b c a14.2321; 13.7476; 19.4973
90; 90; 90		3814.8Chan, Chieh-Kai; Lai, Chien-Yu; Wang, Cheng-Chung
TMSOTf-catalyzed synthesis of substituted quinazolines using hexamethyldisilazane as a nitrogen source under neat and microwave irradiation conditions.
Organic & biomolecular chemistry, 2020, 18, 7201-7212
7157695 CIFC10 H12 I N3P b c a13.9563; 10.5922; 15.5819
90; 90; 90		2303.44Byrne, Joseph P.; Albrecht, Martin
Anion-cation synergistic metal-free catalytic oxidative homocoupling of benzylamines by triazolium iodide salts.
Organic & biomolecular chemistry, 2020, 18, 7379-7387
7157696 CIFC10 H12 B F4 N3P b c a14.4577; 10.5526; 15.7197
90; 90; 90		2398.3Byrne, Joseph P.; Albrecht, Martin
Anion-cation synergistic metal-free catalytic oxidative homocoupling of benzylamines by triazolium iodide salts.
Organic & biomolecular chemistry, 2020, 18, 7379-7387
7157697 CIFC10 H12 I3 N3C 1 2/c 120.4846; 9.4451; 15.8942
90; 99.242; 90		3035.3Byrne, Joseph P.; Albrecht, Martin
Anion-cation synergistic metal-free catalytic oxidative homocoupling of benzylamines by triazolium iodide salts.
Organic & biomolecular chemistry, 2020, 18, 7379-7387
7157698 CIFC31 H23 ClP 1 21/n 112.1573; 12.3663; 15.5243
90; 107.422; 90		2226.9Wei, Hao-Zhao; Li, Quan-Zhe; Wei, Yin; Shi, Min
Rapid construction of cyclopenta[<i>b</i>]naphthalene frameworks from propargylic alcohol tethered methylenecyclopropanes.
Organic & biomolecular chemistry, 2020, 18, 7396-7400
7157699 CIFC26 H21 ClP n a 2120.7442; 12.396; 7.5295
90; 90; 90		1936.17Wei, Hao-Zhao; Li, Quan-Zhe; Wei, Yin; Shi, Min
Rapid construction of cyclopenta[<i>b</i>]naphthalene frameworks from propargylic alcohol tethered methylenecyclopropanes.
Organic & biomolecular chemistry, 2020, 18, 7396-7400
7157700 CIFC1.9 H1.9 Cl0.1 F0.3 N0.1 O0.2 S0.1P -18.692; 10.4626; 12.9164
106.067; 98.907; 110.261		1017.1Wang, Xiaonan; Gao, Yuan; Wei, Zhonglin; Cao, Jungang; Liang, Dapeng; Lin, Yingjie; Duan, Haifeng
Enantioselective addition of thiols to trifluoromethyl ketimines: synthesis of <i>N</i>,<i>S</i>-ketals.
Organic & biomolecular chemistry, 2020, 18, 7431-7436
7157701 CIFC37 H34 N2 O8 S2C 1 2 134.292; 8.1908; 16.147
90; 111.061; 90		4232.4Song, Yong-Xing; Lin, Ye; Yan, Li; Du, Da-Ming
An organocatalytic domino Michael addition strategy: construction of bispiro[oxindole-thiazolidinone-hexahydroxanthone]s with five contiguous stereocenters.
Organic & biomolecular chemistry, 2020, 18, 7373-7378
7157702 CIFC53 H80 N4 O13P 1 21 114.4086; 13.7833; 14.4694
90; 110.157; 90		2697.59Stadelmann, Thomas; Subramanian, Govindan; Menon, Sanjay; Townsend, Chad E.; Lokey, R. Scott; Ebert, Marc-Olivier; Riniker, Sereina
Connecting the conformational behavior of cyclic octadepsipeptides with their ionophoric property and membrane permeability.
Organic & biomolecular chemistry, 2020, 18, 7110-7126
7157703 CIFC118 H198 K3 N11 O36 S3P 114.9008; 15.8307; 16.8469
111.244; 101.429; 100.095		3495.22Stadelmann, Thomas; Subramanian, Govindan; Menon, Sanjay; Townsend, Chad E.; Lokey, R. Scott; Ebert, Marc-Olivier; Riniker, Sereina
Connecting the conformational behavior of cyclic octadepsipeptides with their ionophoric property and membrane permeability.
Organic & biomolecular chemistry, 2020, 18, 7110-7126
7157704 CIFC21 H21 N O3P 1 21/n 18.3648; 24.4988; 8.6463
90; 106.405; 90		1699.73Qiao, Shanshan; Qian, Peng-Cheng; Chen, Fan; Cheng, Jiang
Iron-catalyzed radical cascade 6-<i>endo</i> cyclization of dienes towards fused nitrogen heterocycles initiated by an alkoxycarbonyl radical.
Organic & biomolecular chemistry, 2020, 18, 7086-7089
7157705 CIFC27 H20 N2 O8 SP -17.6399; 11.119; 15.958
70.281; 78.966; 74.305		1221Sathi, Vidya; Thomas, Noble V.; Deepthi, Ani
Stereoselective synthesis of dispiro heterocycles by [3 + 2] cycloaddition of azomethine ylides with a thiazolo[3,2-<i>a</i>]indole derivative.
Organic & biomolecular chemistry, 2020, 18, 7822-7826
7157706 CIFC28 H21 F N2 O2 S SeP 1 21/n 113.215; 11.927; 15.344
90; 101.15; 90		2372.8Yao, Hai-Feng; Wang, Dian-Liang; Li, Fang-Hui; Wu, Bing; Cai, Zhong-Jian; Ji, Shun-Jun
Synthesis of organoselenyl isoquinolinium imides <i>via</i> iron(III) chloride-mediated tandem cyclization/selenation of <i>N</i>'-(2-alkynylbenzylidene)hydrazides and diselenides.
Organic & biomolecular chemistry, 2020, 18, 7577-7584
7157707 CIFC16 H9 Cl N2 OP 1 21/c 122.757; 4.748; 23.677
90; 104.854; 90		2472.8Chen, Junrong; Li, Zhenmin; Suleman, Muhammad; Wang, Zaibin; Lu, Ping; Wang, Yanguang
TfOH-promoted synthesis of 4,5-dihydrooxazolo[5,4-<i>c</i>]isoquinolines <i>via</i> formal [3 + 2] cycloaddition of 4-diazoisoquinolin-3-one and benzonitriles.
Organic & biomolecular chemistry, 2020, 18, 7671-7676
7157708 CIFC23 H20 N2 O SP 1 21/n 17.7469; 17.4348; 14.3624
90; 92.609; 90		1937.9Zhang, Xuxue; Liu, Chuan; Deng, Yupian; Cao, Song
Chemo- and regioselective synthesis of polysubstituted 2-aminothiophenes by the cyclization of <i>gem</i>-dibromo or <i>gem</i>-dichloroalkenes with β-keto tertiary thioamides.
Organic & biomolecular chemistry, 2020, 18, 7540-7544
7157709 CIFC18 H18 F3 N O3 SP -15.6871; 8.6686; 18.3693
81.037; 88.297; 87.959		893.7Bonciolini, Stefano; Di Filippo, Mara; Baumann, Marcus
A scalable continuous photochemical process for the generation of aminopropylsulfones.
Organic & biomolecular chemistry, 2020, 18, 9428-9432
7157710 CIFC19 H24 O6P 1 21 19.4888; 7.2783; 12.988
90; 97.094; 90		890.12Chang, Fang-Rong; Wang, Shih-Wei; Chen, Shu-Rong; Lee, Ching-Ying; Sheu, Jyh-Horng; Cheng, Yuan-Bin
Aleuritin, a novel dinor-diterpenoid from the twigs of <i>Aleurites moluccanus</i> with an anti-lymphangiogenic effect.
Organic & biomolecular chemistry, 2020, 18, 7892-7898
7157711 CIFC18 H24 O3P 21 21 217.0307; 8.666; 25.171
90; 90; 90		1533.6Chang, Fang-Rong; Wang, Shih-Wei; Chen, Shu-Rong; Lee, Ching-Ying; Sheu, Jyh-Horng; Cheng, Yuan-Bin
Aleuritin, a novel dinor-diterpenoid from the twigs of <i>Aleurites moluccanus</i> with an anti-lymphangiogenic effect.
Organic & biomolecular chemistry, 2020, 18, 7892-7898
7157712 CIFC20 H28 O2P 21 21 217.526; 13.1519; 17.4059
90; 90; 90		1722.9Chang, Fang-Rong; Wang, Shih-Wei; Chen, Shu-Rong; Lee, Ching-Ying; Sheu, Jyh-Horng; Cheng, Yuan-Bin
Aleuritin, a novel dinor-diterpenoid from the twigs of <i>Aleurites moluccanus</i> with an anti-lymphangiogenic effect.
Organic & biomolecular chemistry, 2020, 18, 7892-7898
7157713 CIFC19 H16 N2 O4P n a 217.6762; 12.3159; 17.1409
90; 90; 90		1620.49Choi, Jin Ho; Kim, Kunyoung; Oh, Harin; Han, Sangil; Mishra, Neeraj Kumar; Kim, In Su
Ru(ii)-Catalyzed C-H addition and oxidative cyclization of 2-aryl quinazolinones with activated aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9611-9622
7157714 CIFC37 H38 N2 O3 SP 1 21/n 112.3228; 13.5824; 19.942
90; 104.136; 90		3236.7Kumaran, Subramani; Prabhakaran, Mohan; Mariyammal, Narayanan; Parthasarathy, Kanniyappan
Catalyst-free 1,6-conjugate addition of indoles and 4-hydroxycoumarins to <i>para</i>-quinone methides: synthesis of unsymmetrical triarylmethanes.
Organic & biomolecular chemistry, 2020, 18, 7837-7841
7157715 CIFC16 H15 Br2 N5 O2P 1 21/n 118.4913; 4.7672; 19.316
90; 94.258; 90		1698.04Galve, Iñaki; Ondoño, Raül; de Rocafiguera, Claudi; Puig de la Bellacasa, Raimon; Batllori, Xavier; Puigjaner, Cristina; Font-Bardia, Mercè; Vallcorba, Oriol; Teixidó, Jordi; Borrell, José I
A captured room temperature stable Wheland intermediate as a key structure for the orthogonal decoration of 4-amino-pyrido[2,3-<i>d</i>]pyrimidin-7(8<i>H</i>)-ones.
Organic & biomolecular chemistry, 2020, 18, 9810-9815
7157716 CIFC32 H26 B2 F9 N3 O2P -111.2245; 13.0227; 13.7251
92.741; 106.371; 107.992		1810.67Moneva Lorente, Pau; Wallabregue, Antoine; Zinna, Francesco; Besnard, Céline; Di Bari, Lorenzo; Lacour, Jérôme
Synthesis and properties of chiral fluorescent helicene-BODIPY conjugates.
Organic & biomolecular chemistry, 2020, 18, 7677-7684
7157717 CIFC15 H11 N O2P 1 21 13.9404; 16.0925; 9.1575
90; 90.254; 90		580.68Bian, Zi-Long; Lv, Xin-Xin; Li, Ya-Lan; Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Acid-promoted synthesis and photophysical properties of substituted acridine derivatives.
Organic & biomolecular chemistry, 2020, 18, 8141-8146
7157718 CIFC19 H13 N O2P n a 2118.7602; 9.1601; 16.7999
90; 90; 90		2887Bian, Zi-Long; Lv, Xin-Xin; Li, Ya-Lan; Sun, Wen-Wu; Liu, Ji-Kai; Wu, Bin
Acid-promoted synthesis and photophysical properties of substituted acridine derivatives.
Organic & biomolecular chemistry, 2020, 18, 8141-8146
7157719 CIFC11 H10 N OP b c a15.014; 10.0228; 21.573
90; 90; 90		3246.4Luo, Yan; Chen, Chun-Hua; Zhu, Fan; Mo, Dong-Liang
Synthesis of α-aminooxy amides through [3 + 3] cycloaddition and Sc(OTf)<sub>3</sub>-catalyzed double C-N bond cleavage in a one-pot reaction.
Organic & biomolecular chemistry, 2020, 18, 8209-8218
7157720 CIFC17 H16 N2 O2P 1 21/c 111.2384; 10.343; 13.5036
90; 107.74; 90		1495Luo, Yan; Chen, Chun-Hua; Zhu, Fan; Mo, Dong-Liang
Synthesis of α-aminooxy amides through [3 + 3] cycloaddition and Sc(OTf)<sub>3</sub>-catalyzed double C-N bond cleavage in a one-pot reaction.
Organic & biomolecular chemistry, 2020, 18, 8209-8218
7157721 CIFC14 H11 N O2P 1 21/c 110.114; 10.3178; 10.5034
90; 102.09; 90		1071.76Gangadurai, Chinnakuzhanthai; Illa, Giri Teja; Reddy, D. Srinivasa
FeCl<sub>3</sub>-catalyzed oxidative decarboxylation of aryl/heteroaryl acetic acids: preparation of selected API impurities.
Organic & biomolecular chemistry, 2020, 18, 8459-8466
7157722 CIFC37 H34 I N O2P -15.8087; 11.2608; 47.001
93.058; 90.358; 92.48		3067Xi, Zhi-Wei; He, Yan; Liu, Li-Qiu; Wang, Ying-Chun
Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical <i>N</i>-aryl dialkynylimines.
Organic & biomolecular chemistry, 2020, 18, 8089-8093
7157723 CIFC23 H40 N2 OP -18.2053; 9.9516; 14.8729
79.118; 88.843; 68.605		1108.86Xi, Zhi-Wei; He, Yan; Liu, Li-Qiu; Wang, Ying-Chun
Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical <i>N</i>-aryl dialkynylimines.
Organic & biomolecular chemistry, 2020, 18, 8089-8093
7157724 CIFC27 H15 F2 NP 1 21/n 15.8348; 14.7954; 21.5626
90; 92.427; 90		1859.79Xi, Zhi-Wei; He, Yan; Liu, Li-Qiu; Wang, Ying-Chun
Palladium-catalyzed double coupling reaction of terminal alkynes with isocyanides: a direct approach to symmetrical <i>N</i>-aryl dialkynylimines.
Organic & biomolecular chemistry, 2020, 18, 8089-8093
7157725 CIFC17 H22 F N O3P -18.6569; 11.7473; 16.347
98.164; 91.884; 90.183		1644.6Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157726 CIFC17 H23 F2 N O3P 1 21 19.0751; 6.1933; 15.1581
90; 98.79; 90		841.95Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157727 CIFC17 H23 F2 N O3P 1 21/c 16.0625; 22.0365; 12.8581
90; 90.522; 90		1717.7Chen, Suo; Ruan, Yao; Lu, Ji-Liang; Hunter, Luke; Hu, Xiang-Guo
Diastereoselective synthesis and conformational analysis of 4,5-difluoropipecolic acids.
Organic & biomolecular chemistry, 2020, 18, 8192-8198
7157728 CIFC24 H21 N3 O2P 1 21/c 19.5144; 13.3582; 16.0144
90; 102.194; 90		1989.43Tang, Shi-Biao; Fu, Xiao-Pan; Wu, Gao-Rong; Zhang, Li-Li; Deng, Ke-Zuan; Yang, Jin-Yue; Xia, Cheng-Cai; Ji, Ya-Fei
Rhodium(III)-catalyzed C4-amidation of indole-oximes with dioxazolones <i>via</i> C-H activation.
Organic & biomolecular chemistry, 2020, 18, 7922-7931
7157729 CIFC12.8 H8.8 N0.4 O0.4P -19.6741; 10.8198; 12.5635
69.234; 89.878; 72.178		1162.2Xu, Fen; Zhu, Wen-Jing; Wang, Juan; Ma, Qi; Shen, Li-Jing
Rhodium-catalyzed synthesis of substituted isoquinolones <i>via</i> a selective decarbonylation/alkyne insertion cascade of phthalimides.
Organic & biomolecular chemistry, 2020, 18, 8219-8223
7157730 CIFC16 H20 O6C 1 2 18.1628; 13.0501; 13.9274
90; 103.346; 90		1443.55Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157731 CIFC16 H20 O5P 21 21 217.2801; 9.9611; 18.9298
90; 90; 90		1372.75Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157732 CIFC16 H20 O5P 21 21 216.8403; 10.54278; 7.78736
90; 90; 90		1382.6Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157733 CIFC16 H18 O3P 21 21 217.1617; 9.7401; 18.6984
90; 90; 90		1304.32Yan, Hai-Wei; Zhang, Xu; Yang, Ya-Nan; Feng, Zi-Ming; Jiang, Jian-Shuang; Zhang, Pei-Cheng
Archromones A-F, unusual polycyclic dearomatic geranylquinol derivatives from the roots of <i>Arnebia euchroma</i>.
Organic & biomolecular chemistry, 2020, 18, 8424-8432
7157734 CIFC19 H20 Cl N O5P 1 21 19.6261; 6.61723; 14.2237
90; 98.0027; 90		897.2Romaniszyn, Marta; Sieroń, Lesław; Albrecht, Łukasz
Asymmetric vinylogous Michael addition of 5-substituted-furan-2(3<i>H</i>)-ones to an α,β-unsaturated-γ-lactam.
Organic & biomolecular chemistry, 2020, 18, 8633-8637
7157735 CIFC40 H52 O11P b c n17.1752; 8.82114; 24.8611
90; 90; 90		3766.58Choo, Yvonne S. L.; Giamberini, Marta; Antonio, José; Waddell, Paul G.; Benniston, Andrew C.
Functionalized fluorescent terephthalate monomers and their attempted polyester formation.
Organic & biomolecular chemistry, 2020, 18, 8735-8745
7157736 CIFC H N OP b c a12.9152; 15.907; 18.038
90; 90; 90		3705.8Liu, Siyuan; Wang, Hang; Wang, Baomin
Catalyst-free construction of spiro [benzoquinolizidine-chromanones] <i>via</i> a tandem condensation/1,5-hydride transfer/cyclization process.
Organic & biomolecular chemistry, 2020, 18, 8839-8843
7157737 CIFC20 H14 N2 OP b c a8.3127; 17.1849; 20.9916
90; 90; 90		2998.71Jaspal, Sonam; Shinde, Vikki N.; Meena, Neha; Nipate, Dhananjay S.; Rangan, Krishnan; Kumar, Anil
Metal-free benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acids.
Organic & biomolecular chemistry, 2020, 18, 9072-9080
7157738 CIFC23 H17 N5 O2P 1 21/n 111.158; 11.434; 15.708
90; 96.925; 90		1989.4Ge, Junying; Ding, Qiuping; Yang, Man; He, Tian; Peng, Yiyuan
Copper and manganese co-mediated cascade aza-Michael addition/cyclization and azidation of 1,3-enynes: regioselective synthesis of fully substituted azido pyrroles.
Organic & biomolecular chemistry, 2020, 18, 8908-8915
7157739 CIFC18 H14 Cl N O3C 1 2/c 129.8793; 7.7831; 12.7135
90; 93.634; 90		2950.6Yugandar, Somaraju; Morita, Taiki; Nakamura, Hiroyuki
Rhodium(III)-catalysed decarboxylative C-H functionalization of isoxazoles with alkenes and sulfoxonium ylides.
Organic & biomolecular chemistry, 2020, 18, 8625-8628
7157740 CIFC26 H24 F N3P 21 21 215.6056; 17.422; 22.161
90; 90; 90		2164.3Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157741 CIFC21 H16 F N3P b c a9.2995; 9.7287; 37.4385
90; 90; 90		3387.1Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157742 CIFC24 H20 F N3 OP 1 21 15.4142; 20.89; 8.3858
90; 92.126; 90		947.8Tiwari, Vibha; Bingham, Jacob T.; Vyas, Shubham; Singh, Anand
Intermolecular fluoroamination of allenes towards substituted vinyl fluorides
Organic & Biomolecular Chemistry, 2020, 18, 9044-9049
7157743 CIFC37 H29 N O4P 110.7714; 11.3185; 13.3343
66.429; 80.647; 75.079		1436.53Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157744 CIFC36 H26 N2 O2P 3112.9632; 12.9632; 16.2424
90; 90; 120		2363.77Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157745 CIFC36 H32 N2 O2P 21 21 219.3208; 15.9714; 19.0521
90; 90; 90		2836.21Yao, Chao; Wu, Piao; Huang, Yue; Chen, Yaoqi; Li, Lin; Li, Yue-Ming
Binaphthyl-based chiral ligands: design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes.
Organic & biomolecular chemistry, 2020, 18, 9712-9725
7157746 CIFC7 H7 Br N2 OP -13.8839; 8.7474; 22.667
81.742; 88.786; 85.859		760.07Li, Yibiao; Huang, Shuo; Li, Jiaming; Li, Jian; Ji, Xiaoliang; Liu, Jiasheng; Chen, Lu; Peng, Shiyong; Zhang, Kun
Access to 2-pyridinylamide and imidazopyridine from 2-fluoropyridine and amidine hydrochloride
Organic & Biomolecular Chemistry, 2020, 18, 9292-9299
7157747 CIFC12 H19 N5 O4P 1 21/c 117.8252; 7.4804; 10.9523
90; 105.159; 90		1409.56Nakaike, Yumi; Yoshida, Yusuke; Yokoyama, Soichi; Ito, Akitaka; Nishiwaki, Nagatoshi
Synthesis and intramolecular ring transformation of N,N′-dialkylated 2,6,9-triazabicyclo[3.3.1]nonadienes
Organic & Biomolecular Chemistry, 2020, 18, 9109-9116
7157748 CIFC20 H19 N5 O4P 1 21/n 114.4032; 9.8582; 19.916
90; 140.02; 90		1817Nakaike, Yumi; Yoshida, Yusuke; Yokoyama, Soichi; Ito, Akitaka; Nishiwaki, Nagatoshi
Synthesis and intramolecular ring transformation of N,N′-dialkylated 2,6,9-triazabicyclo[3.3.1]nonadienes
Organic & Biomolecular Chemistry, 2020, 18, 9109-9116
7157749 CIFC18 H17 N O4 SC 1 c 113.738; 15.885; 7.706
90; 111.13; 90		1569Ahn, Hye-In; Park, Jong-Un; Xuan, Zi; Kim, Ju Hyun
Pd-Catalyzed asymmetric [5 + 2] cycloaddition of vinylethylene carbonates and cyclic imines: access to N-fused 1,3-oxazepines.
Organic & biomolecular chemistry, 2020, 18, 9826-9830
7157750 CIFC11 H13 Cl N4 OP 14.4944; 5.4263; 12.2978
97.735; 94.192; 92.2		296.04Zhang, Yanhua; Lin, Yun; Hou, Qianqian; Liu, Xi; Pricl, Sabrina; Peng, Ling; Xia, Yi
Novel aryltriazole acyclic C-azanucleosides as anticancer candidates.
Organic & biomolecular chemistry, 2020, 18, 9689-9699
7157751 CIFC28 H25 Cl3 N2 O4 SP 1 21/n 19.9981; 15.1043; 18.6398
90; 92.173; 90		2812.85Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157752 CIFC29 H27 Cl3 N2 O4 SC 1 2/c 126.0749; 9.8982; 23.541
90; 105.383; 90		5858.1Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157753 CIFC21 H19 Cl N2 O3C 1 2/c 122.788; 9.824; 19.984
90; 123.49; 90		3731.1Wan, Shu-Hao; Li, Xuan-An; Liu, Yi-Hung; Liu, Shiuh-Tzung
<i>N</i>-Allylation <i>versus C</i>-allylation of intermediates from aza-Michael adducts of arylideneisoxazol-5-ones.
Organic & biomolecular chemistry, 2020, 18, 9516-9525
7157759 CIFC16 H18 Cl N O6P 1 21/a 111.042; 8.8933; 16.9598
90; 95.377; 90		1658.12Bakthadoss, Manickam; Mushaf, Mohammad
Intramolecular [3 + 2] nitrone cycloaddition reaction: highly regio and diastereoselective synthesis of bicyclo[3.2.1]octane scaffolds.
Organic & biomolecular chemistry, 2020, 18, 9653-9659
7157760 CIFC23 H17 N OP 1 21/n 18.8725; 11.6847; 16.8773
90; 102.266; 90		1709.77Shen, Bing-Xue; Min, Xiang-Ting; Hu, Yan-Cheng; Qian, Lei-Lei; Yang, Sa-Na; Wan, Boshun; Chen, Qing-An
Copper-catalyzed boroacylation of allenes to access tetrasubstituted vinylboronates
Organic & Biomolecular Chemistry, 2020, 18, 9253-9260
7157761 CIFC27 H18 N2P 1 21/n 111.8524; 12.1284; 14.3084
90; 107.05; 90		1966.4Huang, Jian; Fu, Yang; Deng, Zhihong; Chen, Wei; Song, Zhibin; Peng, Yiyuan
Rhodium-catalyzed oxidative annulation of 1H-indazoles with alkynes for the synthesis of indazolo[3,2-a]isoquinolines via C-H bond functionalization.
Organic & biomolecular chemistry, 2020, 18, 9863-9872
7157762 CIFC26 H21 Br O5P 1 21/n 111.6835; 10.2297; 18.6723
90; 101.857; 90		2184.07Wang, Ru-Bing; Ren, Xiao-Dong; He, Jie; Zhu, Shan-Shan; Xie, Hui-Ru; Su, Guo-Zhu; Ma, Shuang-Gang; Yu, Shi-Shan
Burchellin and its stereoisomers: total synthesis, structural elucidation and antiviral activity
Organic & Biomolecular Chemistry, 2020, 18, 9081-9087
7157764 CIFC30 H26 N0.25 O4P 1 21/c 110.5825; 10.9351; 20.533
90; 94.269; 90		2369.5Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157765 CIFC152 H108 Cl12 N8 O8 SI 41/a :226.6744; 26.6744; 18.1796
90; 90; 90		12935.2Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157766 CIFC33 H21 Cl3 N2 O4P 1 21/c 114.0142; 21.038; 9.3503
90; 90.176; 90		2756.74Yin, Xinru; Xu, Aimin; Hu, Jidi; Bao, Ming; Hu, Wenhao; Qian, Yu
A Rh(ii)/phosphoric acid co-catalyzed three-component reaction of diazo-ketones with alcohols and azonaphthalenes: access to indole derivatives via a formal [3 + 2]-cycloaddition.
Organic & biomolecular chemistry, 2020, 18, 9805-9809
7157767 CIFC22 H18 Br2 Cl N O3P -18.1923; 10.0872; 13.952
75.123; 88.61; 78.866		1092.9Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157768 CIFC22 H19 Br Cl N O3P 1 21/n 115.6584; 7.2134; 19.131
90; 102.956; 90		2105.8Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157769 CIFC25 H27 N O4P 1 21/c 110.129; 15.539; 15.252
90; 105.482; 90		2313Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157770 CIFC23 H21 Br Cl N O3C 1 2/c 124.318; 9.2383; 20.24
90; 96.433; 90		4518.4Luo, Naili; Liu, Jiamin; Wang, Shan; Wang, Cunde
DBU-promoted ring-opening reactions of multi-substituted donor‒acceptor cyclopropanes: access to functionalized chalcones with a quaternary carbon group
Organic & Biomolecular Chemistry, 2020, 18, 9210-9215
7157771 CIFC39 H53 Br N4 O4 Si3 ZnP -19.3441; 13.5093; 16.7025
98.858; 102.47; 91.92		2029.23Hayashi, Satoshi; Takamatsu, Rina; Takeda, Shiori; Noji, Masahiro; Takanami, Toshikatsu
Central zinc metal-controlled regioselective meso-bromination of zincatedβ-silylporphyrins-rapid access to meso,β-dual-functionalized porphyrins.
Organic & biomolecular chemistry, 2020, 18, 9791-9795
7157772 CIFC43 H39 N3 O8C 1 2/c 141.0905; 12.1637; 21.1598
90; 134.872; 90		7495Li, Chen-Yi; Xiang, Min; Song, Xiang-Jia; Zou, Ying; Huang, Zhi-Cheng; Li, Xia; Tian, Fang; Wang, Li-Xin
A base-catalyzed domino reaction between isoindigos and α-alkylidene succinimides-convenient preparation of highly steric bispirooxindoles.
Organic & biomolecular chemistry, 2020, 18, 9511-9515
7157773 CIFC17 H19 N O3 SP 15.9286; 8.2863; 8.6201
109.21; 90.208; 103.829		386.74Yang, Shuang; Chen, Yuhang; Yuan, Zidan; Bu, Feiyu; Jiang, Cheng; Ding, Zhenhua
Divergent synthesis of oxazolidines and morpholines <i>via</i> PhI(OAc)<sub>2</sub>-mediated difunctionalization of alkenes.
Organic & biomolecular chemistry, 2020, 18, 9873-9882
7157780 CIFC12 H7 N3 SP 1 n 116.216; 8.5645; 16.5649
90; 117.934; 90		2032.52Yang, Zhen; He, Jing; Wei, Yueting; Li, Weiwei; Liu, Ping; Zhao, Jixing; Wei, Yu
NCS-promoted thiocyanation and selenocyanation of pyrrolo[1,2-a]quinoxalines
Organic & Biomolecular Chemistry, 2020, 18, 9088-9094
7157781 CIFC26 H28 O8P -18.3229; 10.5201; 13.8336
88.816; 73.989; 76.976		1133.19Liu, Hongxin; Chen, Shanchong; Zhang, Xiao; Dong, Chunmao; Chen, Yuchan; Liu, Zhaoming; Tan, Haibo; Zhang, Weimin
Structural elucidation, total synthesis, and cytotoxic activity of effphenol A
Organic & Biomolecular Chemistry, 2020, 18, 9035-9038
7157782 CIFC33 H32 Br N O6P -110.102; 10.4727; 15.726
104.702; 94.205; 109.963		1489Jaiswal, Manish K.; Singh, Bhuvnesh; De, Shreemoyee; Singh, Neetu; Singh, Ravi P.
Stereoselective formal [3 + 3] annulation of 3-alkylidene-2-oxindoles with β,γ-unsaturated α-keto esters.
Organic & biomolecular chemistry, 2020, 18, 9852-9862
7157784 CIFC19 H13 N O4P 1 21/c 14.2074; 12.9179; 27.18
90; 94.001; 90		1473.7He, Xue-Wen; Zhou, Wei; Zhang, Min; Tian, Min-Yi; Wang, Hui-Juan; Tian, You-Ping; Liu, Xiong-Li
Transition-metal-free cascade benzannulations for synthesizing 2-hydroxybenzophenones
Organic & Biomolecular Chemistry, 2020, 18, 9039-9043
7157785 CIFC19 H12 Br N O4P 1 21/c 112.5309; 7.1686; 17.8685
90; 94.845; 90		1599.37He, Xue-Wen; Zhou, Wei; Zhang, Min; Tian, Min-Yi; Wang, Hui-Juan; Tian, You-Ping; Liu, Xiong-Li
Transition-metal-free cascade benzannulations for synthesizing 2-hydroxybenzophenones
Organic & Biomolecular Chemistry, 2020, 18, 9039-9043
7157786 CIFC40 H32P -110.4475; 12.2806; 12.3903
100.338; 99.001; 104.084		1483.14Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157787 CIFC12 H12 Br4P 1 21/c 114.8169; 23.135; 13.2408
90; 94.823; 90		4522.7Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157788 CIFC20 H38 O13 P4C 1 2/c 115.6392; 18.8539; 12.4008
90; 127.729; 90		2892Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157789 CIFC18 H24 O4P -16.9814; 11.397; 11.8876
62.708; 82.487; 73.52		806.04Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157790 CIFC12 H16 O4C 1 2/c 111.6744; 9.2737; 11.2747
90; 114.21; 90		1113.3Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157791 CIFC28 H30 N2P 21 21 216.859; 17.0662; 19.6709
90; 90; 90		2302.6Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157792 CIFC44 H36 N12C 1 2/c 123.8429; 14.4588; 12.002
90; 116.455; 90		3704.3Gadigennavar, Savita; Ranganathan, Madhav; Sankararaman, Sethuraman
Which isomer is it, 1,2,5,6- or 1,4,5,8-tetrasubstituted cycloocta-1,3,5,7-tetraene? Synthesis of symmetrically tetrasubstituted cycloocta-1,3,5,7-tetraene derivatives
Organic & Biomolecular Chemistry, 2020, 18, 9284-9291
7157793 CIFC70 H92 O26P 6511.0913; 11.0913; 92.9928
90; 90; 120		9907.06Kikuchi, Takashi; Akita, Keiko; Koike, Hiroki; In, Yasuko; Yamada, Takeshi; Tanaka, Reiko
Carapanins A‒C: new limonoids from andiroba (Carapa guianensis) fruit oil
Organic & Biomolecular Chemistry, 2020, 18, 9268-9274
7157794 CIFC26 H32 O7P 21 21 218.0223; 13.6842; 21.6959
90; 90; 90		2381.75Kikuchi, Takashi; Akita, Keiko; Koike, Hiroki; In, Yasuko; Yamada, Takeshi; Tanaka, Reiko
Carapanins A‒C: new limonoids from andiroba (Carapa guianensis) fruit oil
Organic & Biomolecular Chemistry, 2020, 18, 9268-9274
7157795 CIFC18 H18 N4 O4P 1 21/c 111.1364; 19.9122; 8.5927
90; 107.324; 90		1819Dagar, Anuradha; Kim, Ikyon
Expansion of diazepine heterocyclic chemical space <i>via</i> sequential Knoevenagel condensation-intramolecular aza-Wittig reaction: 2-acyl-4-aryl-5<i>H</i>-pyrrolo[1,2-<i>d</i>][1,4]diazepines.
Organic & biomolecular chemistry, 2020, 18, 9836-9851
7157796 CIFC18 H18 N2 O3P 1 21/n 110.3803; 7.9121; 19.5926
90; 104.061; 90		1560.93Dagar, Anuradha; Kim, Ikyon
Expansion of diazepine heterocyclic chemical space <i>via</i> sequential Knoevenagel condensation-intramolecular aza-Wittig reaction: 2-acyl-4-aryl-5<i>H</i>-pyrrolo[1,2-<i>d</i>][1,4]diazepines.
Organic & biomolecular chemistry, 2020, 18, 9836-9851
7157797 CIFC27 H21 Cl F3 N O7P 1 21/n 113.5978; 14.619; 13.9308
90; 117.095; 90		2465.33Penjarla, Thirupathi Reddy; Kundarapu, Maheshwar; Rangan, Krishnan; Bhattacharya, Anupam
Iodine assisted synthesis of CF<sub>3</sub> appended spirodihydrofuryl/cyclopropyl oxindoles by changing the active methylene sources.
Organic & biomolecular chemistry, 2020, 18, 9623-9631
7157798 CIFC28 H26 F3 N3 O6P 1 21 18.8532; 13.7373; 11.5286
90; 107.761; 90		1335.27Penjarla, Thirupathi Reddy; Kundarapu, Maheshwar; Rangan, Krishnan; Bhattacharya, Anupam
Iodine assisted synthesis of CF<sub>3</sub> appended spirodihydrofuryl/cyclopropyl oxindoles by changing the active methylene sources.
Organic & biomolecular chemistry, 2020, 18, 9623-9631
7157799 CIFC22 H21 N O2 S2P 1 21/n 18.0525; 15.8806; 15.2504
90; 94.189; 90		1945Wu, Jia-Yu; Liao, Wei-Jr; Lin, Xiu-Yi; Liang, Chien-Fu
A facile access to <i>N</i>-sulfonylthioimidates and their use for the transformation to 3,4-dihydroquinazolines.
Organic & biomolecular chemistry, 2020, 18, 8881-8885
7157800 CIFC20 H14 Cl N OP -18.0991; 10.0866; 10.5705
75.779; 69.449; 67.461		740.63Zheng, Jing; He, Xiaojie; Xu, Hong; Liu, Hua; Yang, Weiran
A formal [3 + 2] annulation reaction of propargyl sulfonium compounds and <i>N</i>-ylides: access to pyrrolo[2,1-<i>a</i>]quinolines, pyrrolo[2,1-<i>a</i>]phthalazines and indolizines.
Organic & biomolecular chemistry, 2020, 18, 8867-8875
7157801 CIFC2.5 H2 Cl0.33 O0.67P 1 21/c 111.3742; 18.028; 7.5166
90; 106.736; 90		1476.02Xie, Zhen-Zhen; Deng, Zhi-Xiong; Zheng, Yu; Chen, Yan-Shan; Xiao, Jun-An; Chen, Kai; Xiang, Hao-Yue; Yang, Hua
A phosphine-mediated domino sequence of salicylaldehyde with but-3-yn-2-one: rapid access to chromanone.
Organic & biomolecular chemistry, 2020, 18, 8916-8920
7157802 CIFC24 H19 Br N2 O3 SP -18.1722; 10.5252; 13.3654
80.905; 79.401; 76.274		1089.82Feng, Jiajun; He, Tiantong; Xie, Yuxing; Yu, Yang; Baell, Jonathan B.; Huang, Fei
I<sub>2</sub>-Promoted [4 + 2] cycloaddition of <i>in situ</i> generated azoalkenes with enaminones: facile and efficient synthesis of 1,4-dihydropyridazines and pyridazines.
Organic & biomolecular chemistry, 2020, 18, 9483-9493

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