Crystallography Open Database

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1553497 CIFC19 H17 N O4P -18.125; 9.328; 11.408
90.91; 96.19; 107.69		817.8Dai, Jie; Ren, Wenlong; Chang, Wenju; Zhang, Ping; Shi, Yian
An effective route to β2-amino acid derivatives via Pd-catalyzed regioselective hydrocarboxylation of 1,2-disubstituted enimides
Organic Chemistry Frontiers, 2017, 4, 297
1553519 CIFC36 H32 F2 N2 O2P 21 21 2111.5593; 14.0068; 17.8914
90; 90; 90		2896.78Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng
Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles
Organic Chemistry Frontiers, 2017, 4, 57
1553520 CIFC44 H50 N2P 1 21/c 119.661; 10.71; 17.118
90; 97.306; 90		3575Zhu, Zi-Qi; Yin, Lei; Wang, Yang; Shen, Yang; Li, Can; Mei, Guang-Jian; Shi, Feng
Diastereo- and enantioselective construction of biologically important pyrrolo[1,2-a]indole scaffolds via catalytic asymmetric [3 + 2] cyclodimerizations of 3-alkyl-2-vinylindoles
Organic Chemistry Frontiers, 2017, 4, 57
1553521 CIFC16 H18 O3 SP -16.9478; 9.1969; 11.8012
82.206; 81.643; 75.22		717.55Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553522 CIFC15 H16 O2 SP 1 21/n 17.68603; 23.9176; 7.76261
90; 111.053; 90		1331.76Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553523 CIFC14 H11 N SP 1 21/n 15.7042; 25.743; 7.8069
90; 94.59; 90		1142.71Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553524 CIFC15 H14 O SP 1 21/n 15.7958; 25.4544; 8.3123
90; 93.626; 90		1223.85Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553525 CIFC15 H14 O2 SP 1 21/n 15.611; 25.6833; 8.991
90; 98.982; 90		1279.8Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553526 CIFC14 H11 N O SP 1 21/n 15.67633; 26.8781; 7.7875
90; 95.042; 90		1183.53Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553527 CIFC14 H8 N2 S2P -17.8232; 11.6428; 14.5818
84.863; 83.654; 73.557		1263.68Wang, Yang; Zhang, Xiaofeng; Liu, Haixiong; Chen, Hui; Huang, Deguang
Nickel-catalyzed direct formation of the C–S bonds of aryl sulfides from arylsulfonyl chlorides and aryl iodides using Mn as a reducing agent
Organic Chemistry Frontiers, 2017, 4, 31
1553530 CIFC35 H53 N O3P 1 21 17.455; 11.3624; 18.4877
90; 92.585; 90		1564.44Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing
A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum
Organic Chemistry Frontiers, 2017, 4, 42
1553531 CIFC30 H50 O3P 21 21 216.52391; 12.9427; 31.7963
90; 90; 90		2684.78Li, Zheng-Yu; Qi, Feng-Ming; Zhi, De-Juan; Hu, Qiao-Ling; Liu, Ying-Hong; Zhang, Zhan-Xin; Fei, Dong-Qing
A novel spirocyclic triterpenoid and a new taraxerane triterpenoid from Teucrium viscidum
Organic Chemistry Frontiers, 2017, 4, 42
1553543 CIFC22 H21 N O2P 1 21/n 17.348; 22.781; 11.236
90; 101.092; 90		1845.7Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong
Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides
Organic Chemistry Frontiers, 2017, 4, 77
1553544 CIFC15 H16 N2 O3P 1 21/n 19.3103; 4.8793; 30.741
90; 96.596; 90		1387.3Yu, Wenlong; Zhang, Wei; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong
Cobalt(iii)-catalyzed cross-coupling of enamides with allyl acetates/maleimides
Organic Chemistry Frontiers, 2017, 4, 77
1553545 CIFC25 H21 N O2 SR 3 c :H33.922; 33.922; 11.008
90; 90; 120		10970Gong, Xinxing; Li, Guangming; Wu, Jie
Synthesis of polycyclic sultams via a palladium-catalyzed reaction of 1-bromo-2-(cyclopropylidenemethyl)benzenes with 2-alkynylbenzenesulfonamides
Organic Chemistry Frontiers, 2017, 4, 14
1553547 CIFC18 H12 Br2P 1 21/n 15.3248; 17.2473; 7.6729
90; 96.167; 90		700.59Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553548 CIFC20 H16 Br2P 1 21/c 16.6723; 8.653; 15.099
90; 111.66; 90		810.2Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553549 CIFC28 H16 Br2C 1 2/c 121.802; 4.9336; 18.875
90; 90.188; 90		2030.2Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553550 CIFC36 H32 Br2P -110.0648; 11.6684; 12.2462
77.981; 86.017; 79.287		1381.44Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553551 CIFC34 H28 Br2P 1 21/n 111.131; 10.249; 11.763
90; 101.301; 90		1315.92Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553552 CIFC50 H38P -110.8252; 13.5794; 14.2122
114.377; 91.316; 95.604		1889.2Wilbuer, J.; Grenz, D. C.; Schnakenburg, G.; Esser, B.
Donor- and acceptor-functionalized dibenzo[a,e]pentalenes: modulation of the electronic band gap
Organic Chemistry Frontiers, 2017, 4, 658
1553554 CIFC18 H15 I O SeC 1 2/c 120.3; 5.882; 27.651
90; 94.075; 90		3293Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson
Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives
Organic Chemistry Frontiers, 2017, 4, 277
1553555 CIFC20 H19 I O SeP 1 2/c 119.0809; 5.7136; 17.2112
90; 100.175; 90		1846.87Pistoia, Renan P.; Roehrs, Juliano A.; Back, Davi F.; Zeni, Gilson
Iodine-mediated regioselective 5-endo-dig electrophilic cyclization reaction of selenoenynes: synthesis of selenophene derivatives
Organic Chemistry Frontiers, 2017, 4, 277
1553556 CIFC29 H25 Cl N2 O8 SP 1 21 111.4186; 9.7011; 13.152
90; 92.473; 90		1455.5He, Fu-Sheng; Li, Cong-Shan; Deng, Hua; Zheng, Xing; Yang, Zhong-Tao; Deng, Wei-Ping
The facile and stereoselective synthesis of pyrrolidine β-amino acids via copper(i)-catalyzed asymmetric 1,3-dipolar cycloaddition
Organic Chemistry Frontiers, 2017, 4, 52
1553557 CIFC25 H18 O2P n 21 a14.3717; 5.917; 21.4597
90; 90; 90		1824.88Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.
Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans
Organic Chemistry Frontiers, 2017, 4, 972
1553558 CIFC20 H14 OP 21 21 217.9447; 10.3826; 17.0108
90; 90; 90		1403.16Sreenivasulu, Chinnabattigalla; Gopi Krishna Reddy, A.; Satyanarayana, G.
Oxidative annulations triggered by a simple Lewis acid: facile synthesis of benzofurans
Organic Chemistry Frontiers, 2017, 4, 972
1553559 CIFC27 H31 N O7 S3P 1 21/c 121.226; 8.2493; 16.985
90; 109.61; 90		2801.6Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei
tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes
Organic Chemistry Frontiers, 2017, 4, 135
1553560 CIFC15 H21 N O3 SC 1 2/c 125.961; 5.793; 22.2512
90; 114.088; 90		3055Chen, Fei; Zhou, Neng-Neng; Zhan, Jun-Long; Han, Bing; Yu, Wei
tert-Butyl nitrite-mediated vicinal sulfoximation of alkenes with sulfinic acids: a highly efficient approach toward α-sulfonyl ketoximes
Organic Chemistry Frontiers, 2017, 4, 135
1553561 CIFC18 H16 F3 N O2 S2P -16.52; 8.149; 18.175
102.278; 95.21; 97.731		927.9Chen, Min-Tao; Tang, Xiang-Ying; Shi, Min
A facile approach for the trifluoromethylthiolation of methylenecyclopropanes
Organic Chemistry Frontiers, 2017, 4, 86
1553562 CIFC17 H15 N O2P -113.451; 14.313; 15.248
86.714; 63.827; 90.014		2629.2Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai
Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles
Organic Chemistry Frontiers, 2017, 4, 124
1553563 CIFC26 H20 Cl N O3P -17.3875; 11.6702; 13.4944
64.647; 82.911; 77.69		1026.5Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai
Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles
Organic Chemistry Frontiers, 2017, 4, 124
1553564 CIFC23 H24 N2 O6 SP -18.5455; 12.047; 12.1501
60.733; 81.883; 87.112		1079.97Rajaguru, Kandasamy; Mariappan, Arumugam; Muthusubramanian, Shanmugam; Bhuvanesh, Nattamai
Divergent reactivity of α-azidochalcones with metal β-diketonates: tunable synthesis of substituted pyrroles and indoles
Organic Chemistry Frontiers, 2017, 4, 124
1553565 CIFC44 H52 N4 S4P -19.3265; 9.7095; 23.593
78.225; 84.998; 75.52		2023.6Xia, Debin; Keerthi, Ashok; An, Cunbin; Baumgarten, Martin
Synthesis of a quinoidal dithieno[2,3-d;2′,3′-d]benzo[2,1-b;3,4-b′]-dithiophene based open-shell singlet biradicaloid
Organic Chemistry Frontiers, 2017, 4, 18
1553566 CIFC20 H21 N O8P 1 21/c 18.101; 19.041; 13.693
90; 107.19; 90		2017.8Zhang, Li; Zhang, Beichen; Jiang, Teng; Lu, Tao; Zhou, Qingfa
Synthesis of tricyclic 3-hydroxyisoindolin-1-ones via triethylamine-catalyzed domino reactions of electron-deficient alkynes with phthalimidomalonate derivatives
Organic Chemistry Frontiers, 2017, 4, 119
1553567 CIFC22 H16 Cl N O2P 1 21/n 111.366; 11.305; 14.788
90; 110.536; 90		1779.4Zhu, Chao-Qun; Deng, Zhuo-Fei; Zhang, Yahong; Wang, You-Qing
Synthesis of 4-substituted 3-(2-hydroxyphenyl)-quinolines through an unexpected iron(iii) chloride promoted reaction of cyclic imine dibenzo[b,f][1,4]oxazepines with alkynes
Organic Chemistry Frontiers, 2017, 4, 196
1553568 CIFC33 H30 N4 O3P 1 21 18.902; 13.209; 12.059
90; 99.65; 90		1397.9Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang
Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst
Organic Chemistry Frontiers, 2017, 4, 101
1553569 CIFC31 H27 Br N4 O3P 21 21 219.662; 12.286; 24.441
90; 90; 90		2901Cheng, Cang; Lu, Xuehe; Ge, Luo; Chen, Jie; Cao, Weiguo; Wu, Xiaoyu; Zhao, Gang
Effective asymmetric vinylogous Mannich reaction of isatin imines with α,α-dicyanoolefins in the presence of a simple chiral amide phosphonium bifunctional phase transfer catalyst
Organic Chemistry Frontiers, 2017, 4, 101
1553570 CIFC25 H23 N O3P 418.4091; 8.4091; 29.3175
90; 90; 90		2073.13Xu, Meng-Meng; Wang, Hai-Qing; Wan, Ying; He, Guofeng; Yan, Jingjing; Zhang, Shu; Wang, Shu-Liang; Shi, Feng
Catalytic asymmetric substitution of ortho-hydroxybenzyl alcohols with tetronic acid-derived enamines: enantioselective synthesis of tetronic acid-derived diarylmethanes
Organic Chemistry Frontiers, 2017, 4, 358
1553571 CIFC15 H17 Cl N2 O3P 21 21 217.2915; 12.7983; 15.9552
90; 90; 90		1488.92Peng, Xiao-Jiao; Ho, Yee Ann; Wang, Zhi-Peng; Shao, Pan-Lin; Zhao, Yu; He, Yun
Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 81
1553572 CIFC15 H11 Cl F3 N3 O3P 21 21 217.74798; 9.1129; 21.719
90; 90; 90		1533.5Hao, Xin-Qi; Wang, Cong; Liu, Shuang-Liang; Wang, Xiao; Wang, Li; Gong, Jun-Fang; Song, Mao-Ping
Cobalt(ii)/(imidazoline–oxazoline)-catalyzed enantioselective Michael addition of 2-acetyl azaarenes to β-CF3-β-disubstituted nitroalkenes
Organic Chemistry Frontiers, 2017, 4, 308
1553573 CIFC14 H13 N3 O SP -17.68; 8.494; 11.449
85.96; 77.314; 66.467		667.9Chen, Jichao; Wang, Tianyu; Wang, Tong; Lin, Aijun; Yao, Hequan; Xu, Jinyi
Copper-catalyzed C5-selective thio/selenocyanation of 8-aminoquinolines
Organic Chemistry Frontiers, 2017, 4, 130
1553574 CIFC19 H23 Br N O3 PP 21 21 29.8916; 26.4389; 7.7778
90; 90; 90		2034.1Wang, Xubin; Wang, Xiaoming; Han, Zhaobin; Wang, Zheng; Ding, Kuiling
Palladium-catalyzed asymmetric allylic amination: enantioselective synthesis of chiral α-methylene substituted β-aminophosphonates
Organic Chemistry Frontiers, 2017, 4, 271
1553575 CIFC153.47 H187.47 Cl4.41 N2 Si8P 41 21 221.2715; 21.2715; 64.3247
90; 90; 90		29105.4Ushiyama, Ayako; Hiroto, Satoru; Yuasa, Junpei; Kawai, Tsuyoshi; Shinokubo, Hiroshi
Synthesis of a figure-eight azahelicene dimer with high emission and CPL properties
Organic Chemistry Frontiers, 2017, 4, 664
1553576 CIFC21 H21 Cl F N O2P 1 21/c 19.4639; 21.8249; 9.3192
90; 104.752; 90		1861.42Li, Jianxiao; Hu, Weigao; Li, Chunsheng; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng
Palladium-catalyzed cascade reaction of haloalkynes with unactivated alkenes for assembly of functionalized oxetanes
Organic Chemistry Frontiers, 2017, 4, 373
1553577 CIFC15 H15 Br O2P 1 21 17.813; 5.321; 15.394
90; 91.594; 90		639.7Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian
Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities
Organic Chemistry Frontiers, 2017, 4, 1084
1553578 CIFC11 H14 Br F O2P 21 21 215.651; 16.364; 38.4918
90; 90; 90		3559Li, Jing; Li, Zequan; Zhang, Xun; Xu, Bing; Shi, Yian
Catalytic enantioselective bromohydroxylation of aryl olefins with flexible functionalities
Organic Chemistry Frontiers, 2017, 4, 1084
1553579 CIFC17 H12 B F2 N5 OC 1 2/c 110.248; 14.634; 11.146
90; 107.352; 90		1595.5Barbon, Stephanie M.; Novoa, Samantha; Bender, Desiree; Groom, Hilary; Luyt, Leonard G.; Gilroy, Joe B.
Copper-assisted azide‒alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates
Organic Chemistry Frontiers, 2017, 4, 178
1553580 CIFC16 H10 Br2 Cl F3P -17.3184; 13.4865; 17.4149
101.672; 94.139; 101.918		1635.33Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553581 CIFC20 H20 Br F3 OP -17.8481; 10.5581; 12.2042
75.472; 72.741; 72.301		905.55Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553582 CIFC20 H20 Br F3 O2P -18.3533; 9.4941; 12.1934
100.216; 97.306; 100.289		923.7Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553583 CIFC18 H15 Br2 F3P b c a16.4974; 6.84171; 28.6498
90; 90; 90		3233.72Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553584 CIFC16 H11 Br2 F3P -17.1399; 9.7404; 22.8361
97.673; 97.146; 106.455		1487.32Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553585 CIFC17 H12 Br F3C 1 2/c 122.8229; 7.4881; 16.5828
90; 102.102; 90		2771Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553586 CIFC19 H17 Br Cl F3P 1 21/c 18.2233; 22.8182; 10.0565
90; 109.447; 90		1779.36Kazakova, Anna N.; Iakovenko, Roman O.; Boyarskaya, Irina A.; Ivanov, Alexander Yu.; Avdontceva, Margarita S.; Zolotarev, Andrei A.; Panikorovsky, Taras L.; Starova, Galina L.; Nenajdenko, Valentine G.; Vasilyev, Aleksander V.
Brominated CF3-allyl alcohols as multicentered electrophiles in TfOH promoted reactions with arenes
Organic Chemistry Frontiers, 2017, 4, 255
1553587 CIFC12 H11 I N2 O2C m c e6.9379; 19.798; 17.773
90; 90; 90		2441.2He, Xin; Xu, Yi-zhu; Kong, Ling-xuan; Wu, Huan-huan; Ji, De-zhong; Wang, Zhi-bin; Xu, Yun-gen; Zhu, Qi-hua
Copper(i) and N-fluorobenzenesulfonimide-mediated direct regioselective halogenation of 8-amidoquinolines on the C5 position
Organic Chemistry Frontiers, 2017, 4, 1046
1553588 CIFC46 H66 Cl2P 1 21/n 110.4263; 10.2668; 40.789
90; 90.6212; 90		4366Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.
Polymerization of acetylene: polyynes, but not carbyne
Organic Chemistry Frontiers, 2017, 4, 668
1553589 CIFC47 H64P -110.3367; 10.4631; 19.275
88.5549; 78.0127; 88.5903		2038.2Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.
Polymerization of acetylene: polyynes, but not carbyne
Organic Chemistry Frontiers, 2017, 4, 668
1553590 CIFC49 H64P 3 1 c14.154; 14.154; 12.123
90; 90; 120		2103.3Prenzel, Dominik; Kirschbaum, Rolf W.; Chalifoux, Wesley A.; McDonald, Robert; Ferguson, Michael J.; Drewello, Thomas; Tykwinski, Rik R.
Polymerization of acetylene: polyynes, but not carbyne
Organic Chemistry Frontiers, 2017, 4, 668
1553591 CIFC20 H13 F7 N2 OP 1 21/c 17.858; 26.656; 8.984
90; 90.001; 90		1881.8Xu, Jun; Qiao, Li; Ying, Beibei; Zhu, Xiaolei; Shen, Chao; Zhang, Pengfei
Transition-metal-free direct perfluoroalkylation of quinoline amides at C5 position through radical cross-coupling under mild conditions
Organic Chemistry Frontiers, 2017, 4, 1116
1553592 CIFC44 H58 N2 Se2 Si4P 1 21/n 114.2771; 14.228; 22.6224
90; 99.427; 90		4533.33Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.
Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties
Organic Chemistry Frontiers, 2017, 4, 682
1553593 CIFC44 H58 N2 S2 Si4P 1 21/n 114.2494; 14.1245; 22.4876
90; 98.8; 90		4472.7Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.
Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties
Organic Chemistry Frontiers, 2017, 4, 682
1553594 CIFC32 H22 Br8 N2P -110.8503; 12.4427; 12.9897
100.306; 91.28; 108.652		1628.82Xiong, Xiaodong; Deng, Chun-Lin; Li, Zhiming; Peng, Xiao-Shui; Wong, Henry N. C.
Quasi-planar diazadithio and diazodiseleno[8]circulenes: synthesis, structures and properties
Organic Chemistry Frontiers, 2017, 4, 682
1553595 CIFC50 H52 N14 O4P 1 21/c 19.842; 21.609; 25.234
90; 91.32; 90		5365.2Zhang, Qian; Wang, Mei-Xiang
Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule
Organic Chemistry Frontiers, 2017, 4, 283
1553596 CIFC54.83 H62.12 Cl1.76 N16.83 O2C 1 2/c 128.402; 9.816; 18.722
90; 90.7; 90		5219.2Zhang, Qian; Wang, Mei-Xiang
Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule
Organic Chemistry Frontiers, 2017, 4, 283
1553597 CIFC54 H60 N16 O2P -19.6636; 15.1098; 18.1939
69.768; 84.466; 84.513		2475.53Zhang, Qian; Wang, Mei-Xiang
Synthesis of hydroxylated azacalix[1]arene[3]pyridines from hydrolysis of high valent arylcopper complexes and conversion to a double azacalix[1]arene[3]pyridine host molecule
Organic Chemistry Frontiers, 2017, 4, 283
1553598 CIFC40 H24 S2P -17.5051; 8.6296; 11.6509
73.729; 77.669; 77.532		697.78Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung
The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices
Organic Chemistry Frontiers, 2017, 4, 675
1553599 CIFC46 H32P n a 2116.8864; 7.4906; 24.7447
90; 90; 90		3129.94Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung
The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices
Organic Chemistry Frontiers, 2017, 4, 675
1553600 CIFC44 H28P -17.597; 8.9994; 11.0344
78.931; 75.805; 83.409		715.94Lo, Yuan-Chih; Ting, Hao-Chun; Li, Ya-Ze; Li, Yi-Hua; Liu, Shun-Wei; Huang, Kuo-Wei; Wong, Ken-Tsung
The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices
Organic Chemistry Frontiers, 2017, 4, 675
1553601 CIFC26 H22 N4 O5 SC 1 2/c 126.478; 8.1615; 23.0582
90; 96.411; 90		4951.7Chen, Dianpeng; Xing, Gangdong; Yao, Jinzhong; Zhou, Hongwei
Applicable β-sulfonium carbanions: facile construction of thiophene derivatives
Organic Chemistry Frontiers, 2017, 4, 1042
1553602 CIFC12 H9 N O S3P b c n7.9629; 16.9905; 18.7808
90; 90; 90		2540.92Chen, Qiao; Lei, Yingjie; Wang, Yanfang; Wang, Chao; Wang, Yanan; Xu, Zhaoqing; Wang, Huan; Wang, Rui
Direct thiocyanation of ketene dithioacetals under transition-metal-free conditions
Organic Chemistry Frontiers, 2017, 4, 369
1553603 CIFC71 H46 B F24 Ir N O PP 21 21 2112.2302; 15.3106; 36.571
90; 90; 90		6848Wang, Qian; Zhang, Zongpeng; Chen, Caiyou; Yang, Hailong; Han, Zhengyu; Dong, Xiu-Qin; Zhang, Xumu
Iridium catalysts with modular axial-unfixed biphenyl phosphine‒oxazoline ligands: asymmetric hydrogenation of α,β-unsaturated carboxylic acids
Organic Chemistry Frontiers, 2017, 4, 627
1553604 CIFC26 H16 Cu N4 O8P 1 21/c 111.1134; 21.1702; 9.8578
90; 101.189; 90		2275.19Baur, Andreas; Bustin, Katelyn A.; Aguilera, Ellen; Petersen, Jeffrey L.; Hoover, Jessica M.
Copper and silver benzoate and aryl complexes and their implications for oxidative decarboxylative coupling reactions
Organic Chemistry Frontiers, 2017, 4, 519
1553605 CIFC16 H11 N O3P 1 21/c 18.269; 9.296; 16.904
90; 93.281; 90		1297.3Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun
Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones
Organic Chemistry Frontiers, 2017, 4, 292
1553606 CIFC22 H15 N O2P b c a8.874; 13.733; 27.215
90; 90; 90		3317Fang, Xinxin; Gao, Shang; Wu, Zijun; Yao, Hequan; Lin, Aijun
Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones
Organic Chemistry Frontiers, 2017, 4, 292
1553607 CIFC19 H12 N2 O4P -18.066; 8.242; 12.157
92.727; 102.604; 98.233		778Li, Yingying; Gao, Mingchun; Liu, Bingxin; Xu, Bin
Copper nitrate-mediated chemo- and regioselective annulation from two different alkynes: a direct route to isoxazoles
Organic Chemistry Frontiers, 2017, 4, 445
1553608 CIFC26 H31 F2 N O3P -19.4574; 9.9936; 14.0156
89.023; 76.071; 71.074		1213.5Xu, Jian; Song, Qiuling
Synthesis of fully-substituted 1,2,3-triazoles via copper(i)-catalyzed three-component coupling of sulfoximines, alkynes and azides
Organic Chemistry Frontiers, 2017, 4, 938
1553609 CIFC41 H40 O11P -19.7469; 13.1171; 17.5212
70.806; 75.292; 73.524		1996.5Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng
Total synthesis of I3,II8-biapigenin and ridiculuflavone A
Organic Chemistry Frontiers, 2017, 4, 578
1553610 CIFC43 H46 O11P -115.1534; 15.8118; 17.7296
68.774; 76.898; 79.352		3832Lu, Kui; Yang, Ke; Jia, Xiaoliang; Gao, Xing; Zhao, Xia; Pan, Guojun; Ma, Yantao; Huang, Qiyao; Yu, Peng
Total synthesis of I3,II8-biapigenin and ridiculuflavone A
Organic Chemistry Frontiers, 2017, 4, 578
1553611 CIFC31 H23 Cl0 N O4P 21 21 219.9046; 10.4946; 23.736
90; 90; 90		2467.2Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding
Organocatalytic C‒C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins
Organic Chemistry Frontiers, 2017, 4, 560
1553612 CIFC30 H21 N O3P 1 21/n 19.263; 16.211; 15.413
90; 91.21; 90		2313.9Xu, Junyu; Cao, Jing; Fang, Chao; Lu, Tao; Du, Ding
Organocatalytic C–C bond activation of cyclopropenones for ring-opening formal [3 + 2] cycloaddition with isatins
Organic Chemistry Frontiers, 2017, 4, 560
1553613 CIFC38.5 H33 Cl O3P -112.3342; 12.422; 20.4886
94.35; 97.642; 100.981		3037.8Zhang, Yuexia; Wu, Xingxing; Hao, Lin; Wong, Zeng Rong; Lauw, Sherman J. L.; Yang, Song; Webster, Richard D.; Chi, Yonggui Robin
Trimerization of enones under air enabled by NHC/NaOtBu via a SET radical pathway
Organic Chemistry Frontiers, 2017, 4, 467
1553614 CIFC13 H12 N2 OP n a 219.077; 10.4; 11.75
90; 90; 90		1109.2Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming
A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines
Organic Chemistry Frontiers, 2017, 4, 510
1553615 CIFC23 H19 N O2 S2P 21 21 218.189; 14.782; 17.421
90; 90; 90		2108.8Guo, Wei-Si; Wang, Yuan-Chao; Dou, Qian; Wen, Li-Rong; Li, Ming
A copper-catalyzed arylation/nucleophilic addition/fragmentation/C–S bond formation cascade: synthesis of bis(arylthio)imines
Organic Chemistry Frontiers, 2017, 4, 510
1553616 CIFC22 H24 S4 Si2P 1 21/c 110.5479; 16.6; 13.9079
90; 92.242; 90		2433.3Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua
Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi
Organic Chemistry Frontiers, 2017, 4, 1019
1553617 CIFC44 H72 Li4 O4 S4 Si4I 41/a :220.763; 20.763; 13.7545
90; 90; 90		5929.6Li, Lu; Li, Bingbing; Li, Chunli; Ma, Zhiying; Xu, Li; Wang, Hua
Selective deprotonation of tetra[3,4]thienylene in the presence of n-BuLi
Organic Chemistry Frontiers, 2017, 4, 1019
1553618 CIFC17 H17 N O4P -15.7832; 10.4921; 12.3215
90.576; 97.913; 93.157		739.28Chen, Hui; Lin, Cong; Xiong, Chunhua; Liu, Zhanxiang; Zhang, Yuhong
One-pot synthesis of fluorescent 2,4-dialkenylindoles by rhodium-catalyzed dual C–H functionalization
Organic Chemistry Frontiers, 2017, 4, 455
1553619 CIFC21 H17 F OP 1 21/c 113.585; 12.569; 9.741
90; 106.741; 90		1592.8Cao, Tongxiang; Chen, Kai; Zhu, Shifa
An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes
Organic Chemistry Frontiers, 2017, 4, 450
1553620 CIFC23 H26 OP 1 21/c 112.3103; 20.299; 6.9248
90; 95.884; 90		1721.3Cao, Tongxiang; Chen, Kai; Zhu, Shifa
An efficient approach to generate aryl carbenes: gold-catalyzed sequential activation of 1,6-diynes
Organic Chemistry Frontiers, 2017, 4, 450
1553621 CIFC60 H28 F20 N6 O2P -112.4994; 13.1859; 16.0253
102.651; 95.439; 92.29		2560.5Almeida, José; Aguiar, António; Leite, Andreia; Silva, André M. N.; Cunha-Silva, Luís; de Castro, Baltazar; Rangel, Maria; Barone, Giampaolo; Tomé, Augusto C.; Silva, Ana M. G.
1,3-Dipolar cycloadditions with meso-tetraarylchlorins ‒ site selectivity and mixed bisadducts
Organic Chemistry Frontiers, 2017, 4, 534
1553622 CIFC23 H30 N4 O2 SiP b c a15.6516; 14.7041; 20.8303
90; 90; 90		4793.9Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553623 CIFC20 H21 N5 O2 SiP -19.4684; 10.4692; 12.771
96.2634; 95.7478; 113.644		1138.27Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553624 CIFC14 H8 Br3 N3P 1 21/n 116.2913; 10.0932; 19.7897
90; 112.895; 90		2997.7Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553625 CIFC21 H34 N4 O2 SiP b c a8.9462; 11.9145; 43.549
90; 90; 90		4641.9Morozova, Maria A.; Yusubov, Mekhman S.; Kratochvil, Bohumil; Eigner, Václav; Bondarev, Alexander A.; Yoshimura, Akira; Saito, Akio; Zhdankin, Viktor V.; Trusova, Marina E.; Postnikov, Pavel S.
Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry
Organic Chemistry Frontiers, 2017, 4, 978
1553626 CIFC25 H20 O4P 1 21/c 111.9761; 15.4866; 11.0055
90; 106.167; 90		1960.46Mao, Wenbin; Zhu, Chen
Efficient synthesis of multiply substituted butenolides from keto acids and terminal alkynes promoted by combined acids
Organic Chemistry Frontiers, 2017, 4, 1029
1553627 CIFC35 H18 Fe O4P -18.8576; 9.515; 15.8743
79.571; 74.479; 86.413		1267.66Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553628 CIFC32 H18 OP 1 21/n 112.737; 10.827; 15.738
90; 105.708; 90		2089.3Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553629 CIFC51 H29 Cl3 O4P 21 21 2110.5417; 14.8356; 24.1274
90; 90; 90		3773.3Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553630 CIFC51 H30 Cl2 OP 1 21/n 112.3541; 20.5251; 15.593
90; 111.562; 90		3677.21Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553631 CIFC51 H30 Cl2P 1 21/n 112.2233; 20.4397; 15.612
90; 111.759; 90		3622.59Cheung, Kwan Yin; Yang, Shuaijun; Miao, Qian
From tetrabenzoheptafulvalene to sp2 carbon nano-rings
Organic Chemistry Frontiers, 2017, 4, 699
1553632 CIFC20 H19 Br N2 O5 SP 21 21 218.8208; 12.857; 18.1141
90; 90; 90		2054.3Yu, Lu; Cheng, Yuyu; Qi, Fei; Li, Rou; Li, Pengfei
Organocatalytic regioselective, diastereoselective, and enantioselective annulation of cyclic 1-azadienes with γ-nitro ketones via 3,4-cyclization
Organic Chemistry Frontiers, 2017, 4, 1336
1553633 CIFC29 H25 N3P -15.768; 9.924; 20.463
100.063; 91.086; 92.46		1151.8Zhao, Fen; Liu, Yaowen; Yang, Shu; Xie, Kai; Jiang, Yubo
Pd-catalyzed selective N(3)-ortho C–H arylation of 1,4-disubstituted 1,2,3-triazoles
Organic Chemistry Frontiers, 2017, 4, 1112
1553634 CIFC21 H15 Br2 N O2P 1 21/n 116.003; 7.036; 16.456
90; 101.876; 90		1813.2Qiu, Guanyinsheng; Li, Yuewen; Ma, Lele; Zhou, Hongwei
KBr/K2S2O8-mediated dibromohydration of N-(2-alkynylaryl)acetamide
Organic Chemistry Frontiers, 2017, 4, 1069
1553635 CIFC33 H31 N O3P 1 21/n 115.552; 9.109; 20
90; 111.508; 90		2636Liu, Feng; Tian, Jiaxin; Liu, Yong; Tao, Chuangan; Zhu, Hao; Zhang, Aina; Xu, Dongfang; Zhao, Baoguo
Decarboxylative Umpolung of conjugated enals to β-carbanions for intramolecular nucleophilic addition to an aldehyde
Organic Chemistry Frontiers, 2017, 4, 1586
1553636 CIFC25 H20 N2 O2 SP 21 21 217.7445; 13.971; 19.15
90; 90; 90		2072Lin, Ye; Liu, Lei; Du, Da-Ming
Squaramide-catalyzed asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles with chalcones for synthesis of pyrrolidinyl spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 1229
1553637 CIFC16 H21 N3 O5P 21 21 218.4855; 15.887; 25.5299
90; 90; 90		3441.7Deng, Tao; Thota, Ganesh Kumar; Li, Yi; Kang, Qiang
Enantioselective conjugate addition of hydroxylamines to α,β-unsaturated 2-acyl imidazoles catalyzed by a chiral-at-metal Rh(iii) complex
Organic Chemistry Frontiers, 2017, 4, 573
1553638 CIFC36 H40 N2 O4P 1 21/c 111.882; 6.1567; 22.083
90; 99.617; 90		1592.8Purc, Anna; Koszarna, Beata; Iachina, Irina; Friese, Daniel H.; Tasior, Mariusz; Sobczyk, Krzysztof; Pędziński, Tomasz; Brewer, Jonathan; Gryko, Daniel T.
The impact of interplay between electronic and steric effects on the synthesis and the linear and non-linear optical properties of diketopyrrolopyrrole bearing benzofuran moieties
Organic Chemistry Frontiers, 2017, 4, 724
1553639 CIFC32 H38 N2 O2 S3P 1 21/c 120.477; 5.2589; 28.0402
90; 101.007; 90		2964Chen, Wangqiao; Nakano, Masahiro; Takimiya, Kazuo; Zhang, Qichun
Selective thionation of naphtho[2,3-b]thiophene diimide: tuning of the optoelectronic properties and packing structure
Organic Chemistry Frontiers, 2017, 4, 704
1553724 CIFC22 H23 Cl N2 O0 RuP -110.445; 14.347; 14.407
82.53; 85.3; 74.55		2060.7Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie
Ruthenium-catalyzed meta-selective C‒H sulfonation of azoarenes with arylsulfonyl chlorides
Organic Chemistry Frontiers, 2017, 4, 1145
1553725 CIFC18 H13 Cl N2 O2 SC 1 2/c 134.644; 7.0976; 13.544
90; 98.63; 90		3292.6Li, Gang; Lv, Xulu; Guo, Kexiao; Wang, Ya; Yang, Suling; Yu, Liuyang; Yu, Yantang; Wang, Junjie
Ruthenium-catalyzed meta-selective C–H sulfonation of azoarenes with arylsulfonyl chlorides
Organic Chemistry Frontiers, 2017, 4, 1145
1553726 CIFC16 H15 N O7P 21 21 2111.4884; 11.9792; 20.8251
90; 90; 90		2866Wang, Junliang; Li, Jianneng; Shen, Xianwang; Dong, Cong; Lin, Jun; Wei, Kun
Asymmetric total synthesis of (−)-δ-lycorane
Organic Chemistry Frontiers, 2017, 4, 1149
1553727 CIFC60 H46 N4.5P -113.8813; 14.4392; 23.5317
95.8618; 105.365; 91.4814		4517.3Kimura, Yosuke; Kawajiri, Ikumi; Ueki, Masanori; Morimoto, Takayuki; Nishida, Jun-ichi; Ikeda, Hiroshi; Tanaka, Mirai; Kawase, Takeshi
A new fluorophore displaying remarkable solvatofluorochromism and solid-state light emission, and serving as a turn-on fluorescent sensor for cyanide ions
Organic Chemistry Frontiers, 2017, 4, 743
1553728 CIFC11 H16 F3 N O2 S2C 1 2 111.5; 10.46; 11.413
90; 95.06; 90		1367.5Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553729 CIFC19 H10 F4 O2 SP 21 21 216.6977; 8.1914; 30.513
90; 90; 90		1674.1Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553730 CIFC15 H15 F3 O5 SP 21 21 217.5426; 13.2312; 15.9887
90; 90; 90		1595.6Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553731 CIFC17 H11 F3 N2 O SP 21 21 218.5502; 11.0835; 16.8212
90; 90; 90		1594.1Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553732 CIFC11 H14 Cl2 F3 N O2 S2P 1 21 17.7869; 10.8732; 8.8809
90; 95.062; 90		749Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553733 CIFC13 H20 F3 N O4 S2P 1 21 112.4266; 8.8229; 15.107
90; 105.7; 90		1594.5Zhang, He; Leng, Xuebing; Wan, Xiaolong; Shen, Qilong
(1S)-(−)-N-Trifluoromethylthio-2,10-camphorsultam and its derivatives: easily available, optically pure reagents for asymmetric trifluoromethylthiolation
Organic Chemistry Frontiers, 2017, 4, 1051
1553734 CIFC101 H110 N4 Ni P Pt0.5P -115.566; 15.831; 17.7553
80.813; 89.907; 88.251		4317.2Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro
meso-to-meso PtII-bridged NiII-porphyrin dimers
Organic Chemistry Frontiers, 2017, 4, 767
1553735 CIFC162 H174 Cl10 N8 Ni2 PtP -116.142; 21.227; 22.446
106.1; 92.132; 93.364		7365Fukui, Norihito; Jiang, Hua-Wei; Osuka, Atsuhiro
meso-to-meso PtII-bridged NiII-porphyrin dimers
Organic Chemistry Frontiers, 2017, 4, 767
1553736 CIFC76 H38 Br N O8P 1 21/n 113.8397; 24.2642; 16.7166
90; 109.444; 90		5293.4Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing
Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R
Organic Chemistry Frontiers, 2017, 4, 750
1553737 CIFC76 H39 N O9P n a 2121.489; 10.179; 22.215
90; 90; 90		4859.2Xu, Dan; Li, Yanbang; Lou, Ning; Gan, Liangbing
Synthesis of homoazafullerene [C59N(CH2)]R and azahomoazafullerene [C59N(NH)]R
Organic Chemistry Frontiers, 2017, 4, 750
1553738 CIFC17 H13 Br N2 O4 SP 1 21/c 117.5147; 7.024; 15.73
90; 114.033; 90		1767.4Pal, Kuntal; Volla, Chandra M. R.
Rhodium-catalyzed denitrogenative transannulation of 1,2,3-triazolyl-carbamates: efficient access to 4-aminooxazolidinones
Organic Chemistry Frontiers, 2017, 4, 1380
1553741 CIFC19 H22 O3C 1 2/c 128.543; 7.309; 16.361
90; 105.04; 90		3296.3Chang, Wenju; Dai, Jie; Li, Jingfu; Shi, Yuan; Ren, Wenlong; Shi, Yian
A facile approach to ketones via Pd-catalyzed sequential carbonylation of olefins with formic acid
Organic Chemistry Frontiers, 2017, 4, 1074
1553742 CIFC11 H8 N O2 SP 1 21/c 15.69674; 8.92923; 19.6982
90; 94.927; 90		998.3Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert
Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties
Organic Chemistry Frontiers, 2017, 4, 861
1553743 CIFC67.5 H66 Cl3 N O2 SP -114.0225; 15.4902; 15.6494
109.303; 105.791; 106.459		2814.2Ammon, Felix; Sauer, Stephanie Theresia; Lippert, Rainer; Lungerich, Dominik; Reger, David; Hampel, Frank; Jux, Norbert
Unexpected formation of [5]helicenes from hexaarylbenzenes containing pyrrole moieties
Organic Chemistry Frontiers, 2017, 4, 861
1553744 CIFC84 H108 Si4P -18.2685; 13.793; 17.645
72.588; 88.716; 77.009		1868.8Bettinger, Holger F.; Einholz, Ralf; Göttler, Andreas; Junge, Marc; Sättele, Marie-Sophie; Schnepf, Andreas; Schrenk, Claudio; Schundelmeier, Simon; Speiser, Bernd
6,6′,11,11′-Tetra((triisopropylsilyl)ethynyl)-anti-[2.2](1,4)tetracenophane: a covalently coupled tetracene dimer and its structural, electrochemical, and photophysical characterization
Organic Chemistry Frontiers, 2017, 4, 853
1553745 CIFC14 H14 N2 O2 SP -16.121; 8.835; 13.265
83.14; 79.6; 72.93		672.8Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng
Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis
Organic Chemistry Frontiers, 2017, 4, 1266
1553746 CIFC15 H17 N3 O4 SP 1 21 18.6132; 7.4744; 12.867
90; 109.429; 90		781.2Wang, Bin; Xu, Tong; Zhu, Lei; Lan, Yu; Wang, Jingdong; Lu, Ning; Wei, Zhonglin; Lin, Yingjie; Duan, Haifeng
Highly enantioselective nitro-Mannich reaction of ketimines under phase-transfer catalysis
Organic Chemistry Frontiers, 2017, 4, 1266
1553747 CIFC30 H24C 1 c 121.7066; 21.7067; 20.1949
90; 122.509; 90		8024.4Takai, Atsuro; Freas, Dylan J.; Suzuki, Toshikane; Sugimoto, Manabu; Labuta, Jan; Haruki, Rie; Kumai, Reiji; Adachi, Shin-ichi; Sakai, Hayato; Hasobe, Taku; Matsushita, Yoshitaka; Takeuchi, Masayuki
The effect of a highly twisted CC double bond on the electronic structures of 9,9′-bifluorenylidene derivatives in the ground and excited states
Organic Chemistry Frontiers, 2017, 4, 650
1553748 CIFC15 H13 N O4 S2P -17.6834; 8.0281; 12.554
85.471; 73.42; 74.044		713.6Zhou, Kaida; Xia, Hongguang; Wu, Jie
Generation of benzosultams via a radical process with the insertion of sulfur dioxide
Organic Chemistry Frontiers, 2017, 4, 1121
1553749 CIFC15 H13 N O4 S2P 1 21/c 18.151; 8.239; 22.94
90; 100.06; 90		1517Zhou, Kaida; Xia, Hongguang; Wu, Jie
Generation of benzosultams via a radical process with the insertion of sulfur dioxide
Organic Chemistry Frontiers, 2017, 4, 1121
1553750 CIFC26 H31 N3 O6P 19.0047; 9.2247; 9.4826
109.875; 108.593; 107.103		626.45Guo, Jing; Lin, Zi-Hui; Chen, Kai-Bin; Xie, Ying; Chan, Albert S. C.; Weng, Jiang; Lu, Gui
Asymmetric amination of 2-substituted indolin-3-ones catalyzed by natural cinchona alkaloids
Organic Chemistry Frontiers, 2017, 4, 1400
1553751 CIFC54 H48 O8P -18.9558; 9.4432; 13.6247
92.926; 95.287; 111		1066.8Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi
Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems
Organic Chemistry Frontiers, 2017, 4, 828
1553752 CIFC66 H72 O6P 1 21/n 111.8673; 14.8352; 15.9367
90; 102.976; 90		2734.08Hirao, Yasukazu; Konishi, Akihito; Kubo, Takashi
Anthroxyl-based biradical: toward the construction of highly stable multi-spin systems
Organic Chemistry Frontiers, 2017, 4, 828
1553753 CIFC41 H27 OC 1 2/c 123.6823; 14.1831; 19.4393
90; 101.921; 90		6388.6Ip, Ho-Wang; Chow, Hak-Fun; Kuck, Dietmar
Electronic and steric effects on the three-fold Scholl-type cycloheptatriene ring formation around a tribenzotriquinacene core
Organic Chemistry Frontiers, 2017, 4, 817
1553754 CIFC18 H16 N2 O2P 1 21/c 112.4244; 8.0614; 14.7164
90; 100.607; 90		1448.78Selvaraju, Manikandan; Wang, Ying-Lien; Sun, Chung-Ming
Ruthenium(ii)-catalyzed C–H alkenylation/annulation cascade for the rapid synthesis of benzoimidazoisoindoles
Organic Chemistry Frontiers, 2017, 4, 1358
1553755 CIFC7.75 H7.75 F7.75 N7.75 O7.75 S7.75P 21 21 218.086; 14.196; 23.304
90; 90; 90		2675Pouambeka, Tony Wheellyam; Zhang, Ge; Zheng, Guang-Fan; Xu, Guo-Xing; Zhang, Qian; Xiong, Tao; Zhang, Qian
Copper-catalyzed oxidative amidation of α,β-unsaturated ketones via selective C‒H or C‒C bond cleavage
Organic Chemistry Frontiers, 2017, 4, 1420
1553756 CIFC27 H21 N O2 S2P 21 21 215.9608; 18.7773; 20.3817
90; 90; 90		2281.3Shi, Qing; Li, Pinhua; Zhang, Yan; Wang, Lei
Visible light-induced tandem oxidative cyclization of 2-alkynylanilines with disulfides (diselenides) to 3-sulfenyl- and 3-selenylindoles under transition metal-free and photocatalyst-free conditions
Organic Chemistry Frontiers, 2017, 4, 1322
1553757 CIFC16 H12 Cl N OP 1 21/c 19.0611; 7.1551; 20.5051
90; 93.684; 90		1326.66Zhang, Zhiguo; Zhang, Yongchao; Huang, Guoqing; Zhang, Guisheng
Organoiodine reagent-promoted intermolecular oxidative amination: synthesis of cyclopropyl spirooxindoles
Organic Chemistry Frontiers, 2017, 4, 1372
1553758 CIFC17 H18 Br F3 N2 O6P 21 21 218.3955; 14.09; 16.7651
90; 90; 90		1983.19Liu, Qiang; Zhao, Kun; Zhi, Ying; Raabe, Gerhard; Enders, Dieter
Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines
Organic Chemistry Frontiers, 2017, 4, 1416
1553759 CIFC23 H22 Br Cl2 N3 O5P 1 21/n 19.593; 15.307; 16.705
90; 93.785; 90		2447.6Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong
Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes
Organic Chemistry Frontiers, 2017, 4, 1289
1553760 CIFC20 H17 Br Cl3 N3 O3P -16.299; 11.774; 14.904
99.608; 94.163; 96.363		1078Chen, Dong-Zhen; Xiao, Wen-Jing; Chen, Jia-Rong
Synthesis of spiropyrazoline oxindoles by a formal [4 + 1] annulation reaction between 3-bromooxindoles and in situ-derived 1,2-diaza-1,3-dienes
Organic Chemistry Frontiers, 2017, 4, 1289
1553761 CIFC17 H16 OP 21 21 217.738; 11.656; 14.0895
90; 90; 90		1270.79Zhang, Bo-Sheng; Hua, Hui-Liang; Gao, Lu-Yao; Liu, Ce; Qiu, Yi-Feng; Zhou, Ping-Xin; Zhou, Zhao-Zhao; Zhao, Jia-Hui; Liang, Yong-Min
Palladium-catalyzed arene C–H activation/ketone C–H functionalization reaction: route to spirodihydroindenones
Organic Chemistry Frontiers, 2017, 4, 1376
1553762 CIFC24 H19 N O2 SC 1 2/c 116.382; 18.322; 14.538
90; 120.472; 90		3760.9Zhang, Pengbo; Gao, Yuzhen; Chen, Su; Tang, Guo; Zhao, Yufen
Direct synthesis of 2-sulfonated 9H-pyrrolo[1,2-a]indoles via NaI-catalyzed cascade radical addition/cyclization/isomerization
Organic Chemistry Frontiers, 2017, 4, 1350
1553763 CIFC14 H12 N2 O3P -17.1026; 7.8866; 11.4159
92.777; 92.263; 114.968		577.75Hong, Longcheng; Ahles, Sebastian; Strauss, Marcel A.; Logemann, Christian; Wegner, Hermann A.
Synthesis of 2,3-diaza-anthraquinones via the bidentate Lewis acid catalysed inverse electron-demand Diels–Alder (IEDDA) reaction
Organic Chemistry Frontiers, 2017, 4, 871
1553764 CIFC25 H22 F I2 N O2 SP -18.7048; 10.5461; 13.9946
82.33; 79.359; 79.1		1233.4Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min
Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines
Organic Chemistry Frontiers, 2017, 4, 1294
1553765 CIFC25 H24 Cl N O2 SP 1 21/c 113.2671; 18.296; 19.283
90; 108.684; 90		4434Wang, Qiang; Jiang, Bo; Yu, Liu-Zhu; Wei, Yin; Shi, Min
Iron-catalyzed or iodine-induced intramolecular halocyclization of N-vinyl-tethered methylenecyclopropanes: facile access to halogenated 1,2-dihydroquinolines
Organic Chemistry Frontiers, 2017, 4, 1294
1553766 CIFC18 H17 N S3P -112.112; 13.064; 13.586
113.51; 114.37; 96.715		1690.6Schneeweis, Arno; Neidlinger, Andreas; Reiss, Guido J.; Frank, Walter; Heinze, Katja; Müller, Thomas J. J.
Radical cation and dication of a 4H-dithieno[2,3-b:3′,2′-e][1,4]-thiazine
Organic Chemistry Frontiers, 2017, 4, 839
1553767 CIFC26 H20 F3 N OP -19.3089; 10.692; 10.826
98.78; 90.325; 108.111		1010.5An, Yuanyuan; Zhang, Jun; Xia, Hongguang; Wu, Jie
Radical cyclization of benzene-tethered 1,7-enynes with aryldiazonium tetrafluoroborates: a facile route to benzo[j]phenanthridines
Organic Chemistry Frontiers, 2017, 4, 1318
1553768 CIFC22 H26 F2 N2 O2P 1 21/c 18.7598; 25.852; 8.8958
90; 96.431; 90		2001.9Liu, Kai; Sui, Lin-Chao; Jin, Qiao; Li, Deng-Yuan; Liu, Pei-Nian
CuBr-mediated radical cascade difluoroacetamidation of acrylamides using α,α-difluoro-α-(TMS)-acetamides
Organic Chemistry Frontiers, 2017, 4, 1606
1553769 CIFC16 H11 F N2 OP 1 21/c 121.229; 3.919; 15.628
90; 105.861; 90		1250.7Ding, Junshuai; Zhang, Yingchao; Li, Jizhen
Nickel-catalyzed selective C-5 fluorination of 8-aminoquinolines with NFSI
Organic Chemistry Frontiers, 2017, 4, 1528
1553770 CIFC20 H12 Cl3 N O0P 1 21/n 111.93574; 7.18231; 19.3705
90; 94.7142; 90		1654.94Li, Jianxiao; An, Yanni; Li, Jiawei; Yang, Shaorong; Wu, Wanqing; Jiang, Huanfeng
Palladium-catalyzed C‒S bond activation and functionalization of 3-sulfenylindoles and related electron-rich heteroarenes
Organic Chemistry Frontiers, 2017, 4, 1590
1553771 CIFC34 H52 Cl4 N16 O2P -19.8942; 11.644; 20.487
87.078; 78.302; 68.651		2152Liang, Dong-Dong; Wang, Mei-Xiang
Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines
Organic Chemistry Frontiers, 2017, 4, 1425
1553772 CIFC5.33 H10 Cl0.67 Co0.33 N2.67 O4P 1 21/c 111.9766; 19.3355; 12.7804
90; 114.734; 90		2688.09Liang, Dong-Dong; Wang, Mei-Xiang
Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines
Organic Chemistry Frontiers, 2017, 4, 1425
1553773 CIFC27 H41 N16 O3.5 S1.5P -113.18; 19.895; 20.59
108.27; 107.63; 90.48		4854Liang, Dong-Dong; Wang, Mei-Xiang
Synthesis and conformational structure of hydrazo-bridged homo calix[2]pyridine[2]triazines
Organic Chemistry Frontiers, 2017, 4, 1425
1553774 CIFC20 H23 B F2 N2 O2P -19.003; 10.762; 11.631
73.19; 69.99; 72.45		987.6Kubota, Yasuhiro; Tsukamoto, Masahiro; Ohnishi, Katsuhiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis and fluorescence properties of novel squarylium–boron complexes
Organic Chemistry Frontiers, 2017, 4, 1522
1553775 CIFC21 H17 Cl F3 N3P 1 21 18.6045; 11.4959; 10.3691
90; 114.544; 90		933Xie, En; Rahman, Abdul; Lin, Xufeng
Asymmetric synthesis of CF3- and indole-containing tetrahydro-β-carbolines via chiral spirocyclic phosphoric acid-catalyzed aza-Friedel–Crafts reaction
Organic Chemistry Frontiers, 2017, 4, 1407
1553776 CIFC22 H17 I N2P 1 21/n 110.326; 9.584; 19.601
90; 104.43; 90		1878.6Liu, Cheng-Kou; Yang, Zhao; Zeng, Yu; Guo, Kai; Fang, Zheng; Li, Bo
Sodium nitrite-promoted aerobic oxidative coupling of aryl methyl ketones with ammonium under metal-free conditions: a facile access to polysubstitution imidazoles
Organic Chemistry Frontiers, 2017, 4, 1508
1553777 CIFC10 H12 O2 SP 21 21 215.7817; 8.2558; 19.972
90; 90; 90		953.3Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin
Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides
Organic Chemistry Frontiers, 2017, 4, 1601
1553778 CIFC17 H19 N O2 SP 1 21 111.3637; 6.0455; 11.3636
90; 98.45; 90		772.2Meng, Ke; Xia, Jingzhao; Wang, Yanzhao; Zhang, Xinghua; Yang, Guoqiang; Zhang, Wanbin
Ir/BiphPHOX-catalyzed asymmetric hydrogenation of 3-substituted 2,5-dihydropyrroles and 2,5-dihydrothiophene 1,1-dioxides
Organic Chemistry Frontiers, 2017, 4, 1601
1553779 CIFC21 H16 N2 O3P c a 2111.0348; 21.2718; 7.2221
90; 90; 90		1695.2Tang, Hai-Tao; Zeng, Jia-Hao; Chen, Jun-Jia; Zhou, Yun-Bing; Li, Ren-Hao; Zhan, Zhuang-Ping
Synthesis of pyrazolo[5,1-a]isoquinolines through copper-catalyzed regioselective bicyclization of N-propargylic sulfonylhydrazones
Organic Chemistry Frontiers, 2017, 4, 1513
1553780 CIFC19 H11 Cl F3 N OC 1 2/c 117.5265; 18.9585; 11.1154
90; 120.995; 90		3166Mishra, Kalpana; Singh, Jay Bahadur; Gupta, Tanu; Singh, Radhey M.
TBAB-catalyzed cascade reactions: facile synthesis of 1-trifluoromethyl-3-alkylidene-1,3-dihydrofuro[3,4-b]quinolines via 5-exo-dig cyclization of o-arylalkynylquinoline aldehydes
Organic Chemistry Frontiers, 2017, 4, 1926
1553781 CIFC2 H4 N4 OP n m a5.0951; 6.0539; 14.8931
90; 90; 90		459.38Wan, Huabin; Li, Hongmin; Xu, Jian; Wu, Zhuang; Liu, Qifan; Chu, Xianxu; Abe, Manabu; Bégué, Didier; Zeng, Xiaoqing
N-Methylcarbamoyl azide: spectroscopy, X-ray structure and decomposition via methylcarbamoyl nitrene
Organic Chemistry Frontiers, 2017, 4, 1839
1553782 CIFC21 H18 F2 O4P n a 2112.326; 11.032; 13.445
90; 90; 90		1828.3Li, Yuewen; Lu, Yiye; Mao, Runyu; Li, Zhiming; Wu, Jie
A photoinduced reaction of perfluoroalkyl halides with 1,3-diarylprop-2-yn-1-ones catalyzed by DABSO
Organic Chemistry Frontiers, 2017, 4, 1745
1553783 CIFC22 H18 Br4 N2P b c a10.7971; 15.2395; 26.1285
90; 90; 90		4299.2Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng
Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives
Organic Chemistry Frontiers, 2017, 4, 1785
1553784 CIFC18 H26 Br2 N2P 1 21/c 16.6642; 19.8278; 14.8224
90; 101.924; 90		1916.3Huang, Zhe; Zhan, Ming; Zhang, Shaoguang; Luo, Qian; Zhang, Wen-Xiong; Xi, Zhenfeng
Synthesis of dibromo- and tetrabromo-bipyrrolines and their corresponding 2,6-diazasemibullvalene derivatives
Organic Chemistry Frontiers, 2017, 4, 1785
1553785 CIFC26 H25 F3 N O SP 21 21 223.66; 10.2673; 10.5398
90; 90; 90		2560.4Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang
Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2017, 4, 1772
1553786 CIFC27 H23 Cl F3 N O3P 21 21 218.5817; 10.4128; 27.6259
90; 90; 90		2468.64Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang
Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2017, 4, 1772
1553787 CIFC15 H16 F3 N O2 SP 21 21 216.2282; 7.0351; 36.2461
90; 90; 90		1588.16Liu, Bing; Zhang, Zhan-Ming; Xu, Bing; Xu, Shan; Wu, Hai-Hong; Liu, Yuanyuan; Zhang, Junliang
Cu(i)-catalyzed Michael addition of ketiminoesters to β-trifluoromethyl β,β-disubstituted enones: rapid access to 1-pyrrolines bearing a quaternary all-carbon stereocenter
Organic Chemistry Frontiers, 2017, 4, 1772
1553788 CIFC28 H21 N2 O2 PP 1 21/c 112.9056; 8.981; 20.4045
90; 106.848; 90		2263.48Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie
Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides
Organic Chemistry Frontiers, 2017, 4, 1981
1553789 CIFC28 H21 N2 O2 PP 1 21/n 114.3374; 9.71; 18.7718
90; 105.341; 90		2520.22Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie
Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides
Organic Chemistry Frontiers, 2017, 4, 1981
1553790 CIFC29 H23 N2 O3 PP -19.5853; 9.8739; 14.7007
103.11; 94.035; 114.371		1213.1Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie
Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides
Organic Chemistry Frontiers, 2017, 4, 1981
1553791 CIFC28 H21 N2 O2 PP 1 21/c 111.9961; 8.631; 21.6563
90; 95.014; 90		2233.68Qiao, Huijie; Sun, Suyan; Zhang, Yue; Zhu, Hongmei; Yu, Xiaomeng; Yang, Fan; Wu, Yusheng; Li, Zhongxian; Wu, Yangjie
Merging photoredox catalysis with transition metal catalysis: site-selective C4 or C5-H phosphonation of 8-aminoquinoline amides
Organic Chemistry Frontiers, 2017, 4, 1981
1553792 CIFC33 H27 O2 PP 21 21 219.0757; 10.4623; 26.2445
90; 90; 90		2491.99Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua
Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides
Organic Chemistry Frontiers, 2017, 4, 1854
1553793 CIFC32 H25 O PP 1 21/c 112.3885; 18.8197; 10.4583
90; 103.828; 90		2367.66Li, Bin; Zhang, Mingkai; Huang, Xulun; Gu, Zhenhua
Synthesis of 2,3-dihydro-1H-phosphindole-1-oxides via the t-BuLi-mediated rearrangement of vinyl bromides and phosphine oxides
Organic Chemistry Frontiers, 2017, 4, 1854
1553794 CIFC28 H33 B O4P -110.0442; 10.4197; 11.9542
84.471; 84.954; 75.059		1200.58Hsieh, Jen-Chieh; Hong, Ya-Chun; Yang, Chun-Ming; Mannathan, Subramaniyan; Cheng, Chien-Hong
Nickel-catalyzed highly chemo- and stereoselective borylative cyclization of 1,6-enynes with bis(pinacolato)diboron
Organic Chemistry Frontiers, 2017, 4, 1615
1553795 CIFC19 H19 Br O6P 21 21 222.0623; 14.5144; 5.67392
90; 90; 90		1816.91Hao, Xiaoyu; Lin, Lili; Tan, Fei; Ge, Shulin; Liu, Xiaohua; Feng, Xiaoming
Asymmetric synthesis of chromans via the Friedel–Crafts alkylation–hemiketalization catalysed by an N,N′-dioxide scandium(iii) complex
Organic Chemistry Frontiers, 2017, 4, 1647
1553796 CIFC21 H18 Br N O3P 1 21 110.4368; 6.0294; 15.7294
90; 107.537; 90		943.81De Munck, Lode; Sukowski, Verena; Vila, Carlos; Muñoz, M. Carmen; Pedro, José R.
Catalytic enantioselective aza-Reformatsky reaction with seven-membered cyclic imines dibenzo[b,f][1,4]oxazepines
Organic Chemistry Frontiers, 2017, 4, 1624
1553797 CIFC20 H13 F N2 OP 1 21/n 19.17425; 7.88736; 21.7312
90; 99.3556; 90		1551.57Ren, Xuhong; Wang, Qiyang; Yu, Wenjia; Zhan, Xiaoyu; Yao, Yishan; Qin, Bingjie; Dong, Mingxin; He, Xinhua
Photoredox catalytic intramolecular imine C–H bond functionalization using ligand free Cu(ii) salts
Organic Chemistry Frontiers, 2017, 4, 2022
1553798 CIFC7 H9 N7 O9C 1 c 17.6272; 13.3952; 11.846
90; 90.87; 90		1210.1Hou, Tianjiao; Zhang, Jian; Wang, Chenjiao; Luo, Jun
A facile method to construct a 2,4,9-triazaadamantane skeleton and synthesize nitramine derivatives
Organic Chemistry Frontiers, 2017, 4, 1819
1553799 CIFC21 H40 O3 SiP 1 21/c 115.7593; 6.7689; 21.0839
90; 104.622; 90		2176.24Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis
Gold(i)-catalyzed access to neomerane skeletons
Organic Chemistry Frontiers, 2017, 4, 1906
1553800 CIFC22 H26 N4 O6P -18.7959; 10.4916; 13.2932
70.468; 74.252; 71.371		1076.8Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis
Gold(i)-catalyzed access to neomerane skeletons
Organic Chemistry Frontiers, 2017, 4, 1906
1553801 CIFC22 H26 N4 O6P 1 21/n 115.8792; 7.383; 18.5839
90; 94.011; 90		2173.37Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis
Gold(i)-catalyzed access to neomerane skeletons
Organic Chemistry Frontiers, 2017, 4, 1906
1553802 CIFC22 H26 N4 O6P 1 21/c 119.2372; 19.7853; 12.577
90; 107.983; 90		4553.1Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis
Gold(i)-catalyzed access to neomerane skeletons
Organic Chemistry Frontiers, 2017, 4, 1906
1553803 CIFC21 H38 O3 SiP 1 21/n 115.0743; 6.8149; 21.2545
90; 92.709; 90		2181.03Tugny, Coralie; Khaled, Omar; Derat, Etienne; Goddard, Jean-Philippe; Mouriès-Mansuy, Virginie; Fensterbank, Louis
Gold(i)-catalyzed access to neomerane skeletons
Organic Chemistry Frontiers, 2017, 4, 1906
1553804 CIFC28 H29 I O4 SP 1 21/n 112.0087; 17.7464; 12.6045
90; 103.892; 90		2607.6Miao, Maozhong; Xu, Huaping; Luo, Yi; Jin, Mengchao; Chen, Zhengkai; Xu, Jianfeng; Ren, Hongjun
A modular approach to highly functionalized 3-sulfonylfurans via conjugate addition of 3-cyclopropylideneprop-2-en-1-ones with sodium sulfinates and sequential 5-endo-trig iodocyclization
Organic Chemistry Frontiers, 2017, 4, 1824
1553805 CIFC22 H20 O3P -19.8395; 10.7013; 10.8636
114.335; 94.477; 116.312		885.4Shi, Xiaonan; He, Yan; Zhang, Xinying; Fan, Xuesen
Selective syntheses of diversely substituted 2-hydroxy-4′-hydroxybenzophenones through [4 + 2] or [3 + 3] annulation of penta-3,4-dien-2-ones with 3-formylchromones
Organic Chemistry Frontiers, 2017, 4, 1967
1553806 CIFC22 H19 N O5 SP 21 21 218.8173; 14.3926; 15.3659
90; 90; 90		1949.99Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin
Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters
Organic Chemistry Frontiers, 2017, 4, 1858
1553807 CIFC21 H23 N O5 SP 1 21 18.2203; 9.1263; 13.0906
90; 102.302; 90		959.52Xie, Lei; Ma, Hongli; Li, Jiaqi; Yu, Yuan; Qin, Zhaohai; Fu, Bin
Ni(ii)-Catalyzed enantioselective Mukaiyama–Mannich reaction between silyl enol ethers and cyclic N-sulfonyl α-ketiminoesters
Organic Chemistry Frontiers, 2017, 4, 1858
1553808 CIFC62 H102 Cl8 N26 O21 Zn2C 1 2/c 129.3492; 12.5025; 25.3876
90; 113.65; 90		8533.3Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang
Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril
Organic Chemistry Frontiers, 2017, 4, 1799
1553809 CIFC60 H68 Cl8 N26 O28 Zn2C 1 2/c 127.52; 17.25; 18.358
90; 94.006; 90		8694Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang
Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril
Organic Chemistry Frontiers, 2017, 4, 1799
1553810 CIFC58 H94 Cl6 N26 O22 Zn2P -112.2894; 12.4667; 14.986
73.289; 84.747; 62.451		1947.4Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang
Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril
Organic Chemistry Frontiers, 2017, 4, 1799
1553811 CIFC60 H112 Cl10 N26 O28 Zn2P -112.298; 12.903; 15.662
75.259; 70.211; 76.684		2233Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang
Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril
Organic Chemistry Frontiers, 2017, 4, 1799
1553812 CIFC62 H108 Cl10 N26 O28 Zn2P -112.315; 12.875; 15.525
75.131; 70.361; 77.82		2219.6Qu, Yun-Xia; Lin, Rui-Lian; Zhang, Yun-Qian; Zhou, Kai-Zhi; Zhou, Qing-Di; Zhu, Qian-Jiang; Tao, Zhu; Ma, Pei-Hua; Liu, Jing-Xin; Wei, Gang
Endo/exo binding of alkyl and aryl diammonium ions by cyclopentanocucurbit[6]uril
Organic Chemistry Frontiers, 2017, 4, 1799
1553813 CIFC21 H21 Br N2 O2P -15.095; 12.261; 17
73.395; 81.56; 78.69		993Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun
Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines
Organic Chemistry Frontiers, 2017, 4, 1833
1553814 CIFC22 H26 N2 O4P -16.1408; 10.54; 16.567
87.399; 81.181; 79.922		1043.1Yan, Hao; Li, Xincheng; Wang, Chunxiang; Wan, Boshun
Silver-catalyzed cyclization of nitrones with 2-azetine: a radical approach to 2,3-disubstituted quinolines
Organic Chemistry Frontiers, 2017, 4, 1833
1553815 CIFC23 H23 Cl O7P 21 21 216.82668; 9.4989; 34.5079
90; 90; 90		2237.7Yao, Qian; Lin, Lili; Zhang, Hang; Yu, Han; Xiong, Qian; Liu, Xiaohua; Feng, Xiaoming
The asymmetric synthesis of multisubstituted diquinanes via the domino reaction of electron-deficient enynes
Organic Chemistry Frontiers, 2017, 4, 2012
1553816 CIFC19 H17 N O3 SP 1 21/n 17.8333; 8.7742; 23.1441
90; 95.475; 90		1583.46De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M.
TBAF catalyzed one-pot synthesis of allenyl-indoles
Organic Chemistry Frontiers, 2017, 4, 1849
1553817 CIFC20 H16 F3 N O3 SP 18.5679; 12.3701; 18.181
83.843; 89.595; 80.871		1891.4De Nisi, A.; Sierra, S.; Ferrara, M.; Monari, M.; Bandini, M.
TBAF catalyzed one-pot synthesis of allenyl-indoles
Organic Chemistry Frontiers, 2017, 4, 1849
1553818 CIFC15 H10 I2 O4P 1 21/c 114.884; 4.3831; 27.39
90; 117.921; 90		1578.9Tang, Yang; Yu, Qiong; Ma, Shengming
Efficient trifluoromethylation via the cyclopropanation of allenes and subsequent C–C bond cleavage
Organic Chemistry Frontiers, 2017, 4, 1762

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