Crystallography Open Database

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1553856 CIFC81 H82 O10P -112.0438; 14.5042; 22.049
72.623; 76.291; 77.888		3530.8Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553857 CIFC44 H48 O12P 1 21/n 112.791; 20.978; 14.779
90; 98.582; 90		3921Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553858 CIFC90 H125 N3 O10P -113.633; 15.357; 20.965
91.591; 94.087; 111.251		4073.6Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553859 CIFC42 H46 O11P 1 21 114.289; 23.102; 20.977
90; 108.428; 90		6570Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553860 CIFC119 H158 Cl9 O10P -114.89; 18.123; 21.671
81.371; 82.134; 87.707		5726Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553861 CIFC110 H140 O10C 1 2/c 143.045; 21.347; 23.043
90; 104.773; 90		20474Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553862 CIFC82 H85 O12P 1 21 116.77; 21.69; 18.89
90; 93.48; 90		6858Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553863 CIFC75 H110 O10P -116.619; 16.686; 16.858
95.191; 117.822; 114.325		3527.9Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553864 CIFC81 H84 O10P -112.31; 16.48; 18.98
83.427; 80.887; 69.254		3548Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553865 CIFC82 H86 Cl2 O10P -112.2178; 15.0675; 20.9593
78.186; 85.869; 67.284		3483.6Al-Azemi, Talal F.; Mohamod, Abdirahman A.; Vinodh, Mickey; Alipour, Fatemeh H.
A new approach for the synthesis of mono- and A1/A2-dihydroxy-substituted pillar[5]arenes and their complexation with alkyl alcohols in solution and in the solid state
Organic Chemistry Frontiers, 2018, 5, 10
1553872 CIFC30 H30 I N3 O5P 21 21 2112.1518; 12.3848; 19.412
90; 90; 90		2921.5Zhu, Jing-Yan; Yang, Wu-Lin; Liu, Yang-Zi; Shang, Shao-Jing; Deng, Wei-Ping
A copper(i)-catalyzed asymmetric Mannich reaction of glycine Schiff bases with isatin-derived ketimines: enantioselective synthesis of 3-substituted 3-aminooxindoles
Organic Chemistry Frontiers, 2018, 5, 70
1553873 CIFC13 H23 N O4 SP 21 21 216.1598; 8.133; 31.1006
90; 90; 90		1558.07Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun
Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters
Organic Chemistry Frontiers, 2018, 5, 36
1553874 CIFC21 H24 N2 O6 SP 21 21 217.9925; 13.9906; 19.0487
90; 90; 90		2130.02Wang, Zhi-Peng; Wu, Qi; Jiang, Jia; Li, Zi-Rui; Peng, Xiao-Jiao; Shao, Pan-Lin; He, Yun
Catalytic asymmetric synthesis of pyrrolidine derivatives bearing heteroatom-substituted quaternary stereocenters
Organic Chemistry Frontiers, 2018, 5, 36
1553880 CIFC10 H8 Cl N O2P 1 21/c 13.8516; 11.2844; 21.4208
90; 89.074; 90		930.89Ledovskaya, Maria S.; Rodygin, Konstantin S.; Ananikov, Valentine P.
Calcium-mediated one-pot preparation of isoxazoles with deuterium incorporation
Organic Chemistry Frontiers, 2018, 5, 226
1553883 CIFC43 H60 N2 P Sc Si2P -110.8597; 13.0923; 18.0508
75.984; 74.865; 66.722		2247.6Gao, Hongjie; Su, Jianhong; Xu, Pengfei; Xu, Xin
Scandium-catalyzed C(sp3)‒H alkylation of N,N-dimethyl anilines with alkenes
Organic Chemistry Frontiers, 2018, 5, 59
1553884 CIFC19 H20 OP 1 21/c 18.859; 21.377; 8.0979
90; 106.44; 90		1470.9Zang, Wenqing; Wei, Yin; Shi, Min
Gold(i) catalyzed cascade cyclization: intramolecular two-fold nucleophilic addition to vinylidenecyclopropanes (VDCPs)
Organic Chemistry Frontiers, 2018, 5, 197
1553885 CIFC15 H12 Cl2 O2P -16.059; 8.893; 13.346
91.59; 93.75; 108.42		679.9Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian
An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes
Organic Chemistry Frontiers, 2018, 5, 561
1553886 CIFC18 H20 O2P -18.26; 10.221; 10.602
102.5; 107.52; 109.03		756.2Dai, Jie; Ren, Wenlong; Li, Jingfu; Shi, Yian
An effective approach to aryl-substituted propanoic acids via the Pd-catalyzed hydrocarboxylation of stilbenes
Organic Chemistry Frontiers, 2018, 5, 561
1553887 CIFC18 H17 N O3 SP 1 21/c 117.558; 9.331; 9.8891
90; 91.367; 90		1619.71Sun, Deli; Zhang, Ronghua
Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides
Organic Chemistry Frontiers, 2018, 5, 92
1553888 CIFC13 H15 N O3 SP 1 21/c 115.8995; 8.3725; 9.9537
90; 100.406; 90		1303.2Sun, Deli; Zhang, Ronghua
Transition-metal-free, visible-light-induced oxidative cross-coupling for constructing β-acetylamino acrylosulfones from sodium sulfinates and enamides
Organic Chemistry Frontiers, 2018, 5, 92
1553889 CIFC18 H17 Cl N2 O3 SP 1 21/n 113.2285; 9.3407; 14.9536
90; 95.087; 90		1840.4Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo
Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines
Organic Chemistry Frontiers, 2018, 5, 189
1553890 CIFC17 H14 Cl2 N2 O2 SP 1 21/n 111.6687; 8.7574; 17.8369
90; 96.512; 90		1810.9Jiang, Dong-Fang; Hu, Jie-Yu; Hao, Wen-Juan; Wang, Shu-Liang; Tu, Shu-Jiang; Jiang, Bo
Tunable Cu(i)-catalyzed site-selective dehydrogenative amination of β,γ-unsaturated hydrazones for divergent synthesis of pyrazol-4-ones and 1,6-dihydropyradazines
Organic Chemistry Frontiers, 2018, 5, 189
1553891 CIFC27 H35 N O1.5 PC 1 2/c 110.5217; 14.8118; 29.451
90; 94.42; 90		4576.1Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin
The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C‒H activation
Organic Chemistry Frontiers, 2018, 5, 88
1553892 CIFC28 H24 N O2 PC 1 2/c 124.609; 9.508; 21.415
90; 115.972; 90		4504.7Wang, Huanan; Li, Shuaiqi; Wang, Baiquan; Li, Bin
The regioselective synthesis of 2-phosphinoylindoles via Rh(iii)-catalyzed C‒H activation
Organic Chemistry Frontiers, 2018, 5, 88
1553893 CIFC30 H23 Au F3 N4 O3 P SP 1 21/c 111.707; 16.717; 15.157
90; 96.39; 90		2948Huang, Ronghui; Yang, Yongchun; Wang, Duo-Sheng; Zhang, Liang; Wang, Dawei
Where does Au coordinate to N-(2-pyridiyl)benzotriazole: gold-catalyzed chemoselective dehydrogenation and borrowing hydrogen reactions
Organic Chemistry Frontiers, 2018, 5, 203
1553894 CIFC24 H20 N2 O5P 1 21 110.31419; 19.2062; 11.0205
90; 109.532; 90		2057.49Ruan, Sai; Lin, Xiaobin; Xie, Lihua; Lin, Lili; Feng, Xiaoming; Liu, Xiaohua
Asymmetric synthesis of 3-aminodihydrocoumarins via the chiral guanidine catalyzed cascade reaction of azlactones
Organic Chemistry Frontiers, 2018, 5, 32
1553895 CIFC21 H17 Br N2 OP 1 21/n 18.7889; 8.9182; 22.444
90; 91.02; 90		1758.9Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao
Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones
Organic Chemistry Frontiers, 2018, 5, 80
1553896 CIFC15 H14 N2 OP 1 21/n 19.8465; 26.3558; 9.9725
90; 104.267; 90		2508.2Zhang, Qianqian; Song, Chuanjun; Huang, He; Zhang, Kun; Chang, Junbiao
Cesium carbonate promoted cascade reaction involving DMF as a reactant for the synthesis of dihydropyrrolizino[3,2-b]indol-10-ones
Organic Chemistry Frontiers, 2018, 5, 80
1553897 CIFC23 H20 Cl F3 N2 O3P b c a18.1727; 10.5743; 23.813
90; 90; 90		4576Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles
Organic Chemistry Frontiers, 2018, 5, 210
1553898 CIFC20 H24 N2 O4P 1 21/c 118.416; 11.31; 9.759
90; 93.907; 90		2027.9Sun, Yao-Liang; Wei, Yin; Shi, Min
Phosphine catalyzed δ-carbon addition and isomerization of alkynones to ketimines: the preparation of 1,3-diene substituted dihydroquinazolinones and 3-aminooxindoles
Organic Chemistry Frontiers, 2018, 5, 210
1553899 CIFC14 H19 N O3 SP 21 21 215.36821; 11.71337; 21.6232
90; 90; 90		1359.66Reboredo, Silvia; García-Marijuan, Ainara; Uria, Uxue; Reyes, Efraím; Carrillo, Luisa; Ugarriza, Iratxe; Vicario, Jose L.
Highly diastereoselective C →N acyl rearrangement in polysubstituted pyrrolidine 2,2-dicarboxylates. Stereocontrolled synthesis of densely functionalized prolines
Organic Chemistry Frontiers, 2018, 5, 933
1553900 CIFC13 H13 Br N2 OP 1 21/c 19.673; 11.975; 10.6305
90; 96.144; 90		1224.3Zhao, He; Chen, Xiuwen; Jiang, Huanfeng; Zhang, Min
Copper-catalysed dehydrogenative α-C(sp3)‒H amination of tetrahydroquinolines with O-benzoyl hydroxylamines
Organic Chemistry Frontiers, 2018, 5, 539
1553901 CIFC17 H17 N O3P 21 21 216.5337; 8.4509; 26.0879
90; 90; 90		1440.46Xu, Youguo; Zhang, Sheng; Li, Lijun; Wang, Yukang; Zha, Zhenggen; Wang, Zhiyong
l-Phenylalanine potassium catalyzed asymmetric formal [3 + 3] annulation of 2-enoyl-pyridine N-oxides with acetone
Organic Chemistry Frontiers, 2018, 5, 376
1553902 CIFC16 H36 Br Cl3 Fe NP n n a18.4928; 11.5835; 11.4759
90; 90; 90		2458.3Li, Sanliang; Zhu, Bo; Lee, Richmond; Qiao, Baokun; Jiang, Zhiyong
Visible light-induced selective aerobic oxidative transposition of vinyl halides using a tetrahalogenoferrate(iii) complex catalyst
Organic Chemistry Frontiers, 2018, 5, 380
1553903 CIFC24 H13 FP 1 21/n 110.4684; 7.428; 18.7773
90; 90.086; 90		1460.11Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri
Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation
Organic Chemistry Frontiers, 2018, 5, 398
1553904 CIFC24 H14 Cl2C 1 2/c 116.8237; 11.333; 10.2994
90; 114.382; 90		1788.6Shi, Xinzhe; Roisnel, Thierry; Soulé, Jean-François; Doucet, Henri
Synthesis of mono- and di-arylated acenaphthylenes and programmed access to dibenzo[j,l]fluoranthenes via palladium-catalysed C‒H bond functionalisation
Organic Chemistry Frontiers, 2018, 5, 398
1553905 CIFC20 H22 N4 SP 1 21/n 117.47; 5.702; 20.396
90; 114.211; 90		1853Amendola, Valeria; Boiocchi, Massimo; Fabbrizzi, Luigi; La Cognata, Sonia; Legnani, Laura; Lo Presti, Eliana; Mangano, Carlo; Miljkovic, Ana
Anion-induced isomerization of fluorescent semi(thio)carbazones
Organic Chemistry Frontiers, 2018, 5, 391
1553906 CIFC23 H25 N O2C 1 2 117.0278; 8.4534; 14.668
90; 110.034; 90		1983.59Shen, Hong-Qiang; Liu, Cong; Zhou, Ji; Zhou, Yong-Gui
Enantioselective palladium-catalyzed C‒H functionalization of pyrroles using an axially chiral 2,2′-bipyridine ligand
Organic Chemistry Frontiers, 2018, 5, 611
1553907 CIFC25.5 H35 Cl2 Fe N3 O1.5P 1 21 116.1979; 9.8887; 17.2384
90; 100.854; 90		2711.8Chen, Jianhui; Xi, Tuo; Lu, Zhan
10 gram-scale synthesis of a chiral oxazoline iminopyridine ligand and its applications
Organic Chemistry Frontiers, 2018, 5, 247
1553908 CIFC21 H19 Br O2P 1 21/n 18.277; 19.206; 11.294
90; 93.738; 90		1791.6Qi, Jifeng; Zheng, Jing; Cui, Sunliang
Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization
Organic Chemistry Frontiers, 2018, 5, 222
1553909 CIFC26 H28 O2P -18.914; 9.542; 13.652
86.106; 80.322; 67.976		1061Qi, Jifeng; Zheng, Jing; Cui, Sunliang
Facile synthesis of carbo- and heterocycles via Fe(iii)-catalyzed alkene hydrofunctionalization
Organic Chemistry Frontiers, 2018, 5, 222
1553910 CIFC38 H26 N4 O4P b c n21.1618; 11.9414; 23.2097
90; 90; 90		5865.1Zwoliński, K. M.; Sieroń, L.; Eilmes, J.
One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges
Organic Chemistry Frontiers, 2018, 5, 171
1553911 CIFC46 H50 N4 O8 S4 ZnP 1 21 111.2639; 15.6341; 13.7495
90; 110.204; 90		2272.3Zwoliński, K. M.; Sieroń, L.; Eilmes, J.
One-flask synthesis of dibenzotetraaza[14]annulene cyclic congeners bearing buta-1,3-diyne bridges
Organic Chemistry Frontiers, 2018, 5, 171
1553912 CIFC3.8 H2.8 Br0.2 N0.2 O0.4P 1 21/c 117.1209; 6.8257; 14.2218
90; 100.2; 90		1635.72Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong
A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids
Organic Chemistry Frontiers, 2018, 5, 415
1553913 CIFC24 H28 N O2 RhP -18.581; 10.888; 11.352
93.19; 106.92; 90.49		1012.8Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong
A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids
Organic Chemistry Frontiers, 2018, 5, 415
1553914 CIFC2.44 H1.78 N0.22 O0.22P -17.1832; 10.3531; 12.7041
99.499; 102.356; 98.881		892.4Chen, Changjun; Pan, Yixiao; Zhao, Haoqiang; Xu, Xin; Xu, Jianbin; Zhang, Zongyao; Xi, Siqi; Xu, Lijin; Li, Huanrong
A versatile rhodium(iii) catalyst for direct acyloxylation of aryl and alkenyl C‒H bonds with carboxylic acids
Organic Chemistry Frontiers, 2018, 5, 415
1553915 CIFC29 H32 O3C 1 2/c 130.962; 10.076; 20.18
90; 121.016; 90		5395.5Liu, Lina; Yuan, Zhenbo; Pan, Rui; Zeng, Yuye; Lin, Aijun; Yao, Hequan; Huang, Yue
1,6-Conjugated addition-mediated [4 + 1] annulation: an approach to 2,3-dihydrobenzofurans
Organic Chemistry Frontiers, 2018, 5, 623
1553916 CIFC17 H13 Cl N2 O4P -110.1754; 13.7004; 13.8309
119.49; 102.929; 92.342		1609.7Daggupati, Ramana V.; Malapaka, Chandrasekharam
Cu(i)-Catalyzed amidation/imidation of N-arylglycine ester derivatives via C‒N coupling under mild conditions
Organic Chemistry Frontiers, 2018, 5, 788
1553917 CIFC16 H15 N3 O2P -16.0881; 7.8709; 14.5993
86.207; 88.891; 76.774		679.53Zhu, Chuanle; Zeng, Hao; Chen, Fulin; Liu, Chi; Zhu, Rui; Wu, Wanqing; Jiang, Huanfeng
Copper-catalyzed coupling of oxime acetates and aryldiazonium salts: an azide-free strategy toward N-2-aryl-1,2,3-triazoles
Organic Chemistry Frontiers, 2018, 5, 571
1553918 CIFC28 H26 N2P 1 21/c 16.4301; 13.8923; 12.2241
90; 103.031; 90		1063.85Grandl, Markus; Sun, Yu; Pammer, Frank
Electronic and structural properties of N →B-ladder boranes with high electron affinity
Organic Chemistry Frontiers, 2018, 5, 336
1553919 CIFC40 H54 B2 N2P -19.0141; 12.9277; 15.5179
111.75; 98.849; 99.031		1613.9Grandl, Markus; Sun, Yu; Pammer, Frank
Electronic and structural properties of N →B-ladder boranes with high electron affinity
Organic Chemistry Frontiers, 2018, 5, 336
1553920 CIFC40 H54 B2 N2P 1 21/n 117.2519; 10.4002; 18.7527
90; 94.829; 90		3352.73Grandl, Markus; Sun, Yu; Pammer, Frank
Electronic and structural properties of N →B-ladder boranes with high electron affinity
Organic Chemistry Frontiers, 2018, 5, 336
1553921 CIFC44 H56 B2 N2P 1 21 110.7137; 14.9388; 11.2075
90; 101.824; 90		1755.7Grandl, Markus; Sun, Yu; Pammer, Frank
Electronic and structural properties of N →B-ladder boranes with high electron affinity
Organic Chemistry Frontiers, 2018, 5, 336
1553922 CIFC50 H29 B2 F20 N3P 1 2/n 113.3636; 12.765; 15.0491
90; 111.844; 90		2382.85Grandl, Markus; Sun, Yu; Pammer, Frank
Electronic and structural properties of N →B-ladder boranes with high electron affinity
Organic Chemistry Frontiers, 2018, 5, 336
1553923 CIFC60 H38 B2 F20 N2P -111.196; 13.488; 19.102
102.11; 104.06; 108.18		2528Grandl, Markus; Sun, Yu; Pammer, Frank
Electronic and structural properties of N →B-ladder boranes with high electron affinity
Organic Chemistry Frontiers, 2018, 5, 336
1553924 CIFC35 H37 Cl2 N3 O4 S2P 1 21/n 18.616; 21.777; 18.552
90; 100.259; 90		3425Cao, Bo; Wei, Yin; Shi, Min
Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons
Organic Chemistry Frontiers, 2018, 5, 423
1553925 CIFC8 H12 Cl Cu N4 O4P n a 2124.106; 8.4201; 20.584
90; 90; 90		4178Cao, Bo; Wei, Yin; Shi, Min
Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons
Organic Chemistry Frontiers, 2018, 5, 423
1553926 CIFC33 H33 N3 O4 S2C 1 2/c 133.342; 14.1163; 13.8882
90; 113.533; 90		5993Cao, Bo; Wei, Yin; Shi, Min
Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons
Organic Chemistry Frontiers, 2018, 5, 423
1553927 CIFC33 H33 N3 O4 S2P 1 21/c 120.618; 12.7286; 11.5829
90; 96.577; 90		3019.8Cao, Bo; Wei, Yin; Shi, Min
Indium(iii)-catalyzed intramolecular dearomative cycloaddition ofN-sulfonylaziridines to indoles: facile synthesis of tetracyclic pyrroloindoline skeletons
Organic Chemistry Frontiers, 2018, 5, 423
1553928 CIFC36 H29 N3P 1 21/c 116.4746; 9.1306; 19.2167
90; 113.764; 90		2645.5Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.
A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
Organic Chemistry Frontiers, 2018, 5, 595
1553929 CIFC40.35 H35.05 N3 O1.67P -19.0006; 13.4106; 13.9272
73.859; 78.251; 71.617		1519.94Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.
A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
Organic Chemistry Frontiers, 2018, 5, 595
1553930 CIFC39 H29 N3 O2P 1 21/n 19.8591; 17.6789; 16.9614
90; 96.753; 90		2935.83Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.
A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
Organic Chemistry Frontiers, 2018, 5, 595
1553931 CIFC43 H29 N3P 1 21/n 19.7752; 18.4617; 18.0848
90; 102.389; 90		3187.7Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.
A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
Organic Chemistry Frontiers, 2018, 5, 595
1553932 CIFC44 H31 N3 OP 1 21/c 19.9057; 18.2185; 17.9256
90; 94.694; 90		3224.13Filatov, A. S.; Knyazev, N. A.; Ryazantsev, M. N.; Suslonov, V. V.; Larina, A. G.; Molchanov, A. P.; Kostikov, R. R.; Boitsov, V. M.; Stepakov, A. V.
A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
Organic Chemistry Frontiers, 2018, 5, 595
1553933 CIFC10 H15 N O3P 1 c 19.9528; 5.6608; 10.1737
90; 119.444; 90		499.16Peter, Clovis; Geoffroy, Philippe; Miesch, Michel
Highly diastereoselective access to polyfunctionalized 1,3-oxazines promoted by Brønsted/Lewis acids
Organic Chemistry Frontiers, 2018, 5, 566
1553934 CIFC16 H14 O7P -16.934; 9.4461; 12.5549
77.759; 76.1; 88.981		779.63Xu, Li-Chen; Zhou, Peng; Li, Jia-Zhuo; Hao, Wen-Juan; Tu, Shu-Jiang; Jiang, Bo
Thiazolium salt-catalyzed [3 + 2 + 1] cyclization for the synthesis of trisubstituted 2-pyrones using arylglyoxals as a carbonyl source
Organic Chemistry Frontiers, 2018, 5, 753
1553935 CIFC65 H63 F6 N8 O12 P S6P -114.18; 16.43; 16.973
65.7; 71.841; 79.491		3417.8Zhao, Meng-Yao; Guo, Qing-Hui; Wang, Mei-Xiang
Understanding the driving force for the molecular recognition of S6-corona[3]arene[3]pyridazine toward organic ammonium cations
Organic Chemistry Frontiers, 2018, 5, 760
1553936 CIFC26 H28 Cl2 N3 O5 P RuP 21 21 218.4287; 10.7538; 30.9419
90; 90; 90		2804.59de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A.
Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst
Organic Chemistry Frontiers, 2018, 5, 841
1553937 CIFC33 H30 Cl2 N3 O4 P RuP 428.3195; 28.3195; 8.539
90; 90; 90		6848.2de Julián, E.; Menéndez-Pedregal, E.; Claros, M.; Vaquero, M.; Díez, J.; Lastra, E.; Gamasa, P.; Pizzano, A.
Practical synthesis of enantiopure benzylamines by catalytic hydrogenation or transfer hydrogenation reactions in isopropanol using a Ru-pybox catalyst
Organic Chemistry Frontiers, 2018, 5, 841
1553938 CIFC27 H23 N3 OI 41 c d31.825; 31.825; 8.303
90; 90; 90		8410Zhang, Chen; Pi, Junxia; Chen, Shu; Liu, Ping; Sun, Peipei
Construction of a 4H-pyrido[4,3,2-gh]phenanthridin-5(6H)-one skeleton via a catalyst-free radical cascade addition/cyclization using azo compounds as radical sources
Organic Chemistry Frontiers, 2018, 5, 793
1553939 CIFC22 H22 SiP b c a8.8464; 13.6195; 30.1026
90; 90; 90		3626.9Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng
Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)‒Si bond cleavage
Organic Chemistry Frontiers, 2018, 5, 860
1553940 CIFC21 H20 SiP 1 21/n 112.2864; 9.5206; 14.4288
90; 96.731; 90		1676.16Yang, Qi; Liu, Liang; Chi, Yue; Hao, Wei; Zhang, Wen-Xiong; Xi, Zhenfeng
Rhodium-catalyzed intramolecular carbosilylation of alkynes via C(sp3)‒Si bond cleavage
Organic Chemistry Frontiers, 2018, 5, 860
1553941 CIFC23 H22 N2 O7P 19.297; 11.515; 11.957
61.974; 80.333; 67.602		1044.6Han, Jianxin; Niu, Sheng-Tong; Liu, Yushuang; Gan, Lishe; Wang, Tianfu; Lu, Chong-Dao; Yuan, Tao
Robustanoids A and B, two novel pyrrolo[2,3-b]indole alkaloids from Coffea canephora: isolation and total synthesis
Organic Chemistry Frontiers, 2018, 5, 586
1553942 CIFC28 H21 N5 OP -17.483; 12.28; 13.156
73.055; 75.131; 76.779		1102.1Gao, Qinghe; He, Shuang; Wu, Xia; Zhang, Jingjing; Bai, Suping; Wu, Yandong; Wu, Anxin
Selective access to dipyrazolo-fused pyridines via formal [3 + 2 + 1] heteroannulation of methyl ketones with pyrazol-5-amines
Organic Chemistry Frontiers, 2018, 5, 765
1553943 CIFC83 H54 Cl2 N2 O2P -19.6948; 10.6078; 14.8224
105.266; 103.77; 93.623		1415.35Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D.
A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence
Organic Chemistry Frontiers, 2018, 5, 640
1553944 CIFC34 H29 Cl2 N O3P 1 21/c 114.1223; 10.4359; 19.4476
90; 97.282; 90		2843.05Marin, L.; Guillot, R.; Gandon, V.; Schulz, E.; Lebœuf, D.
A diversity-oriented synthesis of cyclopenta[b]pyrroles and related compounds through a calcium(ii)/copper(ii) catalytic sequence
Organic Chemistry Frontiers, 2018, 5, 640
1553945 CIFC13 H9 Br Cl F4 N SP 1 21/c 16.18585; 19.014; 13.0299
90; 104.086; 90		1486.46Das, Prajwalita; Takada, Masahiro; Tokunaga, Etsuko; Saito, Norimichi; Shibata, Norio
Synthesis of pyridine trans-tetrafluoro-λ6-sulfane derivatives via radical addition
Organic Chemistry Frontiers, 2018, 5, 719
1553946 CIFC16 H12 Cl N O2 SC 1 2/c 124.908; 13.4385; 8.7528
90; 93.042; 90		2925.7Zhao, Lang; Liao, Wei-Wei
Pd-Catalyzed intramolecular C‒H addition to the cyano-group: construction of functionalized 2,3-fused thiophene scaffolds
Organic Chemistry Frontiers, 2018, 5, 801
1553947 CIFC16 H18 N2 O2P 1 21/n 19.5527; 12.362; 12.0679
90; 92.577; 90		1423.66Yue, Qiang; Xiao, Zhen; Ran, Ziyao; Yuan, Songdong; Zhang, Qian; Li, Dong
Copper-catalyzed α-C‒H amidation of simple ethers through C(sp3)‒H/N‒H cross dehydrogenative coupling
Organic Chemistry Frontiers, 2018, 5, 967
1553948 CIFC17 H15.5 N2 O3.5 SP 1 21 113.1217; 8.2301; 15.9865
90; 109.525; 90		1627.15Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia
Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters
Organic Chemistry Frontiers, 2018, 5, 929
1553949 CIFC19 H17 F3 N O3.5P 21 21 218.0275; 13.876; 31.686
90; 90; 90		3529.5Huang, Bing-Bing; Wu, Liang; Liu, Ren-Rong; Xing, Ling-Ling; Liang, Ren-Xiao; Jia, Yi-Xia
Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters
Organic Chemistry Frontiers, 2018, 5, 929
1553950 CIFC28 H20 N4P 1 21/c 110.4482; 7.41078; 13.6312
90; 105.538; 90		1016.88Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin
Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes
Organic Chemistry Frontiers, 2018, 5, 1096
1553951 CIFC25 H30 N2 O3.5 RhP -18.5997; 11.3141; 23.5957
89.88; 86.923; 89.086		2292.21Qin, Wen-Bing; Li, Wei-Wei; Zhu, Peng-Fei; Mo, Xiao-Gang; Zhang, Hui-Jun; Wen, Ting-Bin
Rh(iii)-Catalyzed regio- and stereoselective bisindolylation of vinyl acetate: an efficient approach toward (E)-1,2-bis(2-indolyl)ethenes
Organic Chemistry Frontiers, 2018, 5, 1096
1553952 CIFC24 H22 S6 Si2C 1 2/c 131.277; 16.691; 10.668
90; 93.503; 90		5559Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua
Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene
Organic Chemistry Frontiers, 2018, 5, 1257
1553953 CIFC22 H20 S7 Si2P 1 21/c 119.71; 13.215; 10.489
90; 103.753; 90		2653.7Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua
Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene
Organic Chemistry Frontiers, 2018, 5, 1257
1553954 CIFC11 H11 Br S3 SiP n m a12.594; 7.353; 15.175
90; 90; 90		1405.3Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua
Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene
Organic Chemistry Frontiers, 2018, 5, 1257
1553955 CIFC11 H11 Br S3 SiP 1 21/c 111.5286; 15.8164; 8.4588
90; 110.19; 90		1447.6Liu, Xinming; Sun, Huiliang; Xu, Wan; Wan, Shisheng; Shi, Jianwu; Li, Chunli; Wang, Hua
Syntheses and structures of [7]helicene and double helicene based on dithieno[2,3-b:2′,3′-d]thiophene
Organic Chemistry Frontiers, 2018, 5, 1257
1553956 CIFC53 H49 Cl2 N3 O3P 1 21/n 111.566; 31.513; 12.0437
90; 92.279; 90		4386.2Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay
An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones
Organic Chemistry Frontiers, 2018, 5, 1202
1553957 CIFC50.5 H49 Cl I N3 O5C 1 2/c 129.069; 16.647; 23.834
90; 124.203; 90		9538.8Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay
An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones
Organic Chemistry Frontiers, 2018, 5, 1202
1553958 CIFC52 H47 N3 O3P 1 21/n 113.605; 13.333; 23.507
90; 101.393; 90		4180Krishnan, Jagadeesh; Jose, Anu; Sasidhar, B. S.; Suresh, E.; Menon, Rajeev S.; Nair, Vijay
An uncommon multicomponent reaction involving nucleophilic heterocyclic carbenes: facile synthesis of fully substituted cyclopentanones
Organic Chemistry Frontiers, 2018, 5, 1202
1553959 CIFC20 H19 N O2P 1 21/c 17.6879; 13.3936; 15.696
90; 103.359; 90		1572.46Chen, Wei; Zhang, Yicheng; Li, Pinhua; Wang, Lei
tert-Butyl peroxybenzoate mediated formation of 3-alkylated quinolines from N-propargylamines via a cascade radical addition/cyclization reaction
Organic Chemistry Frontiers, 2018, 5, 855
1553960 CIFC51 H51 Cl5 N4 O2 P2 RuP 1 21/c 112.074; 22.964; 17.711
90; 93.931; 90		4899Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj
ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols
Organic Chemistry Frontiers, 2018, 5, 1008
1553961 CIFC22 H28 Cl F6 N4 P RuP n a 2124.447; 12.95; 7.9
90; 90; 90		2501.1Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj
ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols
Organic Chemistry Frontiers, 2018, 5, 1008
1553962 CIFC48 H44 Cl2 N4 P2 RuP 1 21/c 19.679; 19.168; 21.719
90; 91.489; 90		4028Roy, Bivas Chandra; Debnath, Subhankar; Chakrabarti, Kaushik; Paul, Bhaskar; Maji, Milan; Kundu, Sabuj
ortho-Amino group functionalized 2,2′-bipyridine based Ru(ii) complex catalysed alkylation of secondary alcohols, nitriles and amines using alcohols
Organic Chemistry Frontiers, 2018, 5, 1008
1553963 CIFC23 H21 N O2 SP 21 21 218.0484; 10.6055; 21.9053
90; 90; 90		1869.8Li, Yun; Chen, Jingchao; He, Zhenxiu; Qin, Hongyu; Zhou, Yongyun; Khan, Ruhima; Fan, Baomin
Cobalt-catalyzed asymmetric reactions of heterobicyclic alkenes with in situ generated organozinc halides
Organic Chemistry Frontiers, 2018, 5, 1108
1553964 CIFC26 H27 Br O3P 21 21 214.839; 17.596; 8.652
90; 90; 90		2259.1Li, Shoulei; Liu, Bin; Chen, Li; Li, Xin; Cheng, Jin-Pei
N-Heterocyclic carbene promoted enantioselective desymmetrization reaction of diarylalkane-bisphenols
Organic Chemistry Frontiers, 2018, 5, 1101
1553965 CIFC10 H8 N4P 1 21/c 14.3504; 24.437; 8.5476
90; 102.442; 90		887.36Qiao, Kai; Zhang, Dong; Zhang, Kai; Yuan, Xin; Zheng, Ming-Wei; Guo, Tian-Fo; Fang, Zheng; Wan, Li; Guo, Kai
Iron(ii)-catalyzed C-2 cyanomethylation of indoles and pyrroles via direct oxidative cross-dehydrogenative coupling with acetonitrile derivatives
Organic Chemistry Frontiers, 2018, 5, 1129
1553966 CIFC18 H21 N O2 SP 21 21 219.4077; 9.9254; 17.562
90; 90; 90		1639.9Song, Bo; Chen, Mu-Wang; Zhou, Yong-Gui
Synthesis of chiral sultams with two adjacent stereocenters via palladium-catalyzed dynamic kinetic resolution
Organic Chemistry Frontiers, 2018, 5, 1113
1553967 CIFC15 H7 Cl F N OP 1 21/n 18.9388; 9.7832; 13.5584
90; 107.86; 90		1128.54Liu, Jianming; Yan, Xuyang; Liu, Na; Zhang, Yanyan; Zhao, Shufang; Wang, Xiaopei; Zhuo, Kelei; Yue, Yuanyuan
Elemental sulfur accelerated the reactivity of the 3-position of indole for the construction of chromeno[2,3-b]indoles
Organic Chemistry Frontiers, 2018, 5, 1034
1553968 CIFC26 H27 N O3P -19.2089; 10.5763; 10.9769
100.503; 95.221; 91.16		1046.09Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa
A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines
Organic Chemistry Frontiers, 2018, 5, 1160
1553969 CIFC23 H19 F O2P -18.9683; 9.8217; 11.353
75.074; 77.458; 63.345		857.59Luo, Hejiang; Liang, Renxiao; Chen, Lianfen; Jiang, Huanfeng; Zhu, Shifa
A silver-catalyzed three-component reaction via stabilized cation: synthesis of polysubstituted tetrahydronaphthols and tetrahydronaphthylamines
Organic Chemistry Frontiers, 2018, 5, 1160
1553970 CIFC64 H100 N4 Na4 O46C 1 2/c 129.1539; 14.0671; 24.2333
90; 126.156; 90		8024.4Zhang, Yao; Yu, Shang-Bo; Yang, Bo; Wang, Hui; Zhang, Dan-Wei; Li, Zhan-Ting
Ion-pair electrostatic attraction-enhanced donor‒acceptor interactions between the prototypic 1,4-dialkoxybenzene-viologen binding mode in water
Organic Chemistry Frontiers, 2018, 5, 1039
1553971 CIFC10 H9 Br F N O4 SP 1 21/n 18.7382; 5.8569; 23.8346
90; 91.141; 90		1219.58Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li
Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C‒H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams
Organic Chemistry Frontiers, 2018, 5, 1411
1553972 CIFC15 H11 F O5 SP 1 21/n 18.6492; 6.7929; 25.645
90; 98.112; 90		1491.6Wang, Shi-Meng; Li, Chen; Leng, Jing; Bukhari, Syed Nasir Abbas; Qin, Hua-Li
Rhodium(iii)-catalyzed Oxidative Coupling of N-Methoxybenzamides and Ethenesulfonyl fluoride: a C‒H Bond Activation Strategy for the Preparation of 2-Aryl ethenesulfonyl fluorides and Sulfonyl fluoride Substituted γ-Lactams
Organic Chemistry Frontiers, 2018, 5, 1411
1553973 CIFC12 H10 Br N OP 1 21/c 112.062; 4.0452; 21.707
90; 90.12; 90		1059.2Reddy, Ganapam Manohar; Rao, Naidu Sambasiva; Maheswaran, H.
Highly meta-selective halogenation of 2-phenylpyridine with a ruthenium(i) catalyst
Organic Chemistry Frontiers, 2018, 5, 1118
1553974 CIFC24 H25 Cl2 N OP 21 21 218.799; 14.7395; 16.0279
90; 90; 90		2078.7Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives
Organic Chemistry Frontiers, 2018, 5, 1366
1553975 CIFC22 H23 N O SP 21 21 215.6782; 8.5568; 38.5091
90; 90; 90		1871.05Zheng, Long-Sheng; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Ruthenium-catalyzed dynamic kinetic asymmetric transfer hydrogenation: stereoselective access to syn 2-(1,2,3,4-tetrahydro-1-isoquinolyl)ethanol derivatives
Organic Chemistry Frontiers, 2018, 5, 1366
1553976 CIFC21 H20 N4 O4P 1 21/c 110.5329; 10.3187; 18.4305
90; 97.847; 90		1984.4Cao, Wen-Bin; Liu, Bei-Bei; Xu, Xiao-Ping; Ji, Shun-Jun
Cooperation of copper and dioxygen for the site-selective construction of benzo[1,5]diazocin-6(5H)-ones from indoles and enaminone analogues
Organic Chemistry Frontiers, 2018, 5, 1194
1553977 CIFC34 H28 N O6 P SP 21 21 2111.9446; 13.7058; 19.238
90; 90; 90		3149.5Gu, Zheng; Zhou, Ji; Jiang, Guo-Fang; Zhou, Yong-Gui
Synthesis of chiral γ-aminophosphonates through the organocatalytic hydrophosphonylation of azadienes with phosphites
Organic Chemistry Frontiers, 2018, 5, 1148
1553978 CIFC18 H18 O2P 21 21 217.9384; 9.9744; 17.126
90; 90; 90		1356Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy
Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems
Organic Chemistry Frontiers, 2018, 5, 1320
1553979 CIFC18 H18 O3P 1 21/c 112.6396; 9.6186; 11.8318
90; 103.394; 90		1399.33Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy
Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems
Organic Chemistry Frontiers, 2018, 5, 1320
1553980 CIFC14 H15 N O4P 1 21/c 113.13; 12.87; 7.8
90; 105.51; 90		1270Someswarao, B.; P., Rasvan Khan; Reddy, B. Jagan Mohan; B., Sridhar; B., V. Subba Reddy
Tandem Prins-type cyclization for the stereoselective construction of fused polycyclic ring systems
Organic Chemistry Frontiers, 2018, 5, 1320
1554253 CIFC25 H21 Br F3 N3 O4 SP 21 21 218.8119; 10.4134; 27.1396
90; 90; 90		2490.38Zhu, Wen-Run; Chen, Qing; Lin, Ning; Chen, Kai-Bin; Zhang, Zhen-Wei; Fang, Gang; Weng, Jiang; Lu, Gui
Organocatalytic Michael/cyclization cascade reactions of 3-isothiocyanato oxindoles with 3-trifluoroethylidene oxindoles: an approach for the synthesis of 3′-trifluoromethyl substituted 3,2′-pyrrolidinyl-bispirooxindoles
Organic Chemistry Frontiers, 2018, 5, 1375
1554254 CIFC28 H36 O8P 113.986; 14.019; 28.0285
98.119; 91.053; 90.157		5439.5Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua
Asperones A‒E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1‒15
Organic Chemistry Frontiers, 2018, 5, 2432
1554255 CIFC28 H38 O9P 21 21 218.3949; 15.0525; 22.267
90; 90; 90		2813.8Yin, Guo-Ping; Wu, Ya-Rong; Han, Chao; Wang, Xiao-Bing; Gao, Hong-Liang; Yin, Yong; Kong, Ling-Yi; Yang, Ming-Hua
Asperones A‒E, five dimeric polyketides with new carbon skeletons from the fungus Aspergillus sp. AWG 1‒15
Organic Chemistry Frontiers, 2018, 5, 2432
1554256 CIFC37 H42 O11P 21 21 219.34542; 14.58845; 24.65138
90; 90; 90		3360.85Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin
Lithocarpins A‒D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508
Organic Chemistry Frontiers, 2018, 5, 1792
1554257 CIFC38 H43 Cl3 O11P 1 21 112.0999; 8.9388; 17.0397
90; 90.378; 90		1842.95Xu, Jianlin; Tan, Haibo; Chen, Yuchan; Li, Saini; Huang, Zilei; Guo, Heng; Li, Haohua; Gao, Xiaoxia; Liu, Hongxin; Zhang, Weimin
Lithocarpins A‒D: four tenellone-macrolide conjugated [4 + 2] hetero-adducts from the deep-sea derived fungus Phomopsis lithocarpus FS508
Organic Chemistry Frontiers, 2018, 5, 1792
1554258 CIFC21 H28 O4P 1 21 18.8203; 9.95; 11.3663
90; 104.882; 90		964.07Hu, Li-Jun; Cheng, Min-Jing; Cao, Jia-Qing; Zhong, Li-Ping; Hu, Ya-Jian; Wang, Ying; Wang, Lei; Ye, Wen-Cai; Li, Chuang-Chuang
Asymmetric total syntheses of callistrilones B, G and J
Organic Chemistry Frontiers, 2018, 5, 1506
1554259 CIFC27 H26 O5P -19.56; 10.76; 11.542
89.84; 78.84; 80.4		1148Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554260 CIFC11 H13 N O2P b c a5.565; 17.417; 19.97
90; 90; 90		1935.6Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554261 CIFC15 H21 N O2P -110.139; 10.399; 14.357
80.36; 69.86; 89.98		1398.4Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554262 CIFC13 H15 Br O3P 1 21/c 19.9233; 15.1382; 8.9089
90; 105.815; 90		1287.64Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554263 CIFC12 H14 O3P 1 21/c 18.638; 15.409; 8.594
90; 111.43; 90		1064.8Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554264 CIFC13 H14 O3P 1 21/c 19.944; 16.675; 15.179
90; 108.38; 90		2389Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554265 CIFC27 H26 O5P -17.1922; 9.9323; 16.0391
78.066; 84.732; 86.302		1115.04Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554266 CIFC15 H18 O5P 1 21/c 19.9599; 6.7335; 20.4059
90; 93.522; 90		1365.94Ivanov, Konstantin L.; Vatsouro, Ivan M.; Bezzubov, Stanislav I.; Melnikov, Mikhail Ya.; Budynina, Ekaterina M.
Domino construction of a bullataketal core via double bond cleavage in activated dihydrofurans
Organic Chemistry Frontiers, 2018, 5, 1655
1554267 CIFC23 H32 O6P -18.2403; 11.2635; 11.6154
80.692; 75.701; 83.849		1028.38Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang
Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system
Organic Chemistry Frontiers, 2018, 5, 1502
1554268 CIFC13 H20 O4P 1 21/c 110.8545; 11.1988; 10.9655
90; 117.846; 90		1178.59Liu, Mengchen; Cheng, Chuanxu; Xiong, Weiyan; Cheng, Hang; Wang, Jian-Li; Xu, Liang
Total synthesis of C19-diterpenoid alkaloid: construction of a functionalized ABCDE-ring system
Organic Chemistry Frontiers, 2018, 5, 1502
1554269 CIFC76 H104 O26 S3P 1 21 113.7347; 21.989; 13.7372
90; 110.63; 90		3882.8Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554270 CIFC78 H96 N4 O22C 2 2 2110.70154; 27.4281; 26.4591
90; 90; 90		7766.35Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554271 CIFC35 H44 O12P 21 21 219.18292; 12.4621; 28.4369
90; 90; 90		3254.28Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554272 CIFC74 H90 Cl12 O24P 21 21 2115.8696; 16.1185; 32.0556
90; 90; 90		8199.6Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554273 CIFC77.37 H93.1 N4 O24P 110.54064; 14.6009; 14.9312
62.0192; 84.9082; 68.8864		1884.1Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554274 CIFC74 H91 N2 O24P 21 21 2115.2487; 16.1229; 29.1352
90; 90; 90		7163Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554275 CIFC70 H84 O24P 6514.7018; 14.7018; 53.2893
90; 90; 120		9974.97Li, Wan-Shan; Yang, Yang; Liu, Jun-Jun; Shen, Li; Shi, Zhi; Wu, Jun
Scaffold diversity-oriented synthesis of limonoid dimers: discovery of an axially chiral agent within vivoanti-breast cancer activity
Organic Chemistry Frontiers, 2018, 5, 1079
1554276 CIFC42 H49 Cl2 N3 O3 Ru SP 1 21/n 113.3662; 19.3514; 18.2778
90; 107.451; 90		4510Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung
A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect
Organic Chemistry Frontiers, 2018, 5, 1532
1554277 CIFC33 H46 Cl2 N2 O RuP 1 21/c 114.573; 14.783; 16.116
90; 104.49; 90		3361Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung
A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect
Organic Chemistry Frontiers, 2018, 5, 1532
1554278 CIFC36 H44 Cl2 N2 O RuC 1 2/c 126.317; 17.57; 17.431
90; 110.1; 90		7569Sabbasani, Venkata R.; Gupta, Saswata; Young Yun, Sang; Lee, Daesung
A general approach for the formation of oxygen-chelated ruthenium alkylidene complexes relying on the Thorpe‒Ingold effect
Organic Chemistry Frontiers, 2018, 5, 1532
1554279 CIFC16 H9 N5P 1 21/c 117.5111; 18.0998; 8.8623
90; 98.023; 90		2781.39Xin, Jing-Rui; He, Yan-Hong; Guan, Zhi
Metal-free aerobic oxidative direct C‒H amination of electron-deficient alkenes via photoredox catalysis
Organic Chemistry Frontiers, 2018, 5, 1684
1554280 CIFC20 H14 N2 O2P c a 2116.9028; 16.5253; 9.9901
90; 90; 90		2790.5Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian
Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives
Organic Chemistry Frontiers, 2018, 5, 1679
1554281 CIFC9 H6 N OC 1 2/c 113.3145; 13.4792; 7.0709
90; 93.942; 90		1266Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian
Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives
Organic Chemistry Frontiers, 2018, 5, 1679
1554282 CIFC20 H16 N2 O2P c a 2117.23; 8.7235; 9.6499
90; 90; 90		1450.4Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian
Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives
Organic Chemistry Frontiers, 2018, 5, 1679
1554283 CIFC24 H20 N2 O2P 1 21/n 18.0334; 24.561; 9.1052
90; 105.603; 90		1730.3Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian
Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives
Organic Chemistry Frontiers, 2018, 5, 1679
1554284 CIFC32 H22 N2 O2P -15.3397; 12.5882; 17.165
95.56; 94.461; 101.447		1119.93Yao, Wei; Sun, Mingtai; Zhang, Yuannian; Yang, Hui; Liang, Dong; Wu, Haixia; Ni, Runyan; Wong, Ming Wah; Huang, Dejian
Photo-induced C‒H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives
Organic Chemistry Frontiers, 2018, 5, 1679
1554285 CIFC21 H14 OP 1 21/c 19.533; 17.215; 11.031
90; 122.95; 90		1519.1Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo
Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones
Organic Chemistry Frontiers, 2018, 5, 1613
1554286 CIFC17 H14 OP -18.166; 9.066; 9.404
85.402; 75.824; 71.601		640.5Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo
Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones
Organic Chemistry Frontiers, 2018, 5, 1613
1554287 CIFC27 H18 OP -19.603; 10.694; 10.7294
70.55; 64.18; 81.02		935.2Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo
Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones
Organic Chemistry Frontiers, 2018, 5, 1613
1554288 CIFC31 H20 OP -18.4085; 9.35; 14.153
105.907; 95.411; 97.753		1050.2Guo, Weijie; Wu, Shutao; Wang, Tao; Xie, Qingxiao; Duan, Yulian; Luo, Siyuan; Wang, Jianhui; Yu, Xiaobo
Rhodium-catalyzed decarbonylative cycloadditions of 1H-indene-1,2,3-triones and alkynes via direct C‒C bond activation: divergent synthesis of indenones and quinones
Organic Chemistry Frontiers, 2018, 5, 1613
1554289 CIFC3.93 H3.28 Br0.13 N0.26 O0.26P 1 21/c 123.315; 11.3915; 18.4957
90; 93.135; 90		4905Wang, Chao-Ming; Song, Dan; Xia, Peng-Ju; Ye, Zhi-Peng; Xiao, Jun-An; Xiang, Hao-Yue; Chen, Xiao-Qing; Yang, Hua
Photoredox-catalyzed direct aminoalkylation of isatins: diastereoselective access to 3-hydroxy-3-aminoalkylindolin-2-ones analogues
Organic Chemistry Frontiers, 2018, 5, 1608
1554290 CIFC26 H21 N3 O2P 1 21/n 17.6842; 19.978; 13.7517
90; 98.473; 90		2088Chen, Wei; Ji, Dong-Sheng; Luo, Yong-Chun; Wang, Zhu-Yin; Xu, Peng-Fei
Directing group assisted ZnI2-catalyzed cyclopropanation of indoles via 2-furylcarbenoids
Organic Chemistry Frontiers, 2018, 5, 1768
1554291 CIFC11 H14 O2 S2C 1 2 127.4221; 5.1994; 19.0212
90; 121.717; 90		2306.99Liu, Yan; Zeng, Jing; Sun, Jiuchang; Cai, Lei; Zhao, Yueqi; Fang, Jing; Hu, Bo; Shu, Penghua; Meng, Lingkui; Wan, Qian
1,4-Dithiothreitol mediated cleavage of the acetal and ketal type of diol protecting groups
Organic Chemistry Frontiers, 2018, 5, 2427
1554292 CIFC25 H20 N2 O3P -19.0455; 9.948; 11.7172
94.495; 95.25; 98.331		1034.4Li, Bingnan; Mai, Shaoyu; Song, Qiuling
Synthesis of fused benzimidazoles via successive nucleophilic additions of benzimidazole derivatives to arynes under transition metal-free conditions
Organic Chemistry Frontiers, 2018, 5, 1639
1554293 CIFC34 H31 N O5P 1 21/n 110.3357; 23.6593; 11.6006
90; 104.704; 90		2743.9Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel
Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor‒acceptor oxiranes and aziridines
Organic Chemistry Frontiers, 2018, 5, 2020
1554294 CIFC36 H36 N2 O4P 1 21/c 110.9629; 9.8209; 27.4846
90; 91.397; 90		2958.3Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel
Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor‒acceptor oxiranes and aziridines
Organic Chemistry Frontiers, 2018, 5, 2020
1554295 CIFC44 H44 Cl2 N2 O6 SP c a 2118.1688; 18.3501; 11.8464
90; 90; 90		3949.6Alajarin, Mateo; Bañon, Daniel; Egea, Adrian; Marín-Luna, Marta; Orenes, Raul-Angel; Vidal, Angel
Accessing polysubstituted oxazolidines, pyrrolidines and imidazolidines by regioselective [3 + 2] annulations of ketenimines with donor‒acceptor oxiranes and aziridines
Organic Chemistry Frontiers, 2018, 5, 2020
1554296 CIFC23 H24 N2 O4 S2P 1 21/c 112.143; 10.204; 18.499
90; 94.972; 90		2283.5Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo
Reductive ortho C‒H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles
Organic Chemistry Frontiers, 2018, 5, 1756
1554297 CIFC21 H22 N2 O2 S2P 1 21/c 19.0286; 24.083; 10.3285
90; 114.965; 90		2036Luo, Fan; Lu, Yu; Hu, Mengjie; Tian, Junsong; Zhang, Lei; Bao, Wangzhen; Yan, Chao; Huang, Xin; Wang, Zhi-Xiang; Peng, Bo
Reductive ortho C‒H cyanoalkylation of aryl(heteroaryl) sulfoxides: a general approach to α-aryl(heteroaryl) nitriles
Organic Chemistry Frontiers, 2018, 5, 1756
1554298 CIFC26 H39 Cl2 Co N3 O12P 21 21 2110.4066; 26.417; 12.0692
90; 90; 90		3318Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554299 CIFC26 H39 Cl2 N3 Ni O12P 21 21 2110.3907; 11.9429; 26.537
90; 90; 90		3293.1Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554300 CIFC22 H18 OP 1 21 16.96436; 7.91974; 15.2392
90; 92.2266; 90		839.9Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554301 CIFC26 H41 Cl2 Fe N3 O12P 21 21 2110.3081; 11.98; 26.1548
90; 90; 90		3229.88Zhang, Heyi; Lu, Zhan
Nickel-catalyzed enantioselective sequential Nazarov cyclization/decarboxylation
Organic Chemistry Frontiers, 2018, 5, 1763
1554302 CIFC15 H19 N O3 SP 1 21/c 110.0093; 14.3918; 10.7208
90; 104.176; 90		1497.32Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing
Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives
Organic Chemistry Frontiers, 2018, 5, 2040
1554303 CIFC15 H19 N O3 SP 1 21/c 16.54242; 22.4359; 10.03319
90; 102.165; 90		1439.65Yu, Ji-cong; Yu, Le-mao; Zhao, Xiao-yun; Gan, Lu; Zhu, Wei-wei; Wang, Ze-chen; Wang, Rui; Jiang, Xianxing
Organocatalytic asymmetric [3 + 2] annulation of 1,4-dithiane-2,5-diol with azlactones: access to chiral dihydrothiophen-2(3H)-one derivatives
Organic Chemistry Frontiers, 2018, 5, 2040
1554304 CIFC17 H18 Cl N O2P 1 21 15.9758; 8.5937; 15.7695
90; 93.352; 90		808.45Hu, Yang; Yin, Xuguang; Chen, Ziyi; Dong, Xiu-Qin; Zhang, Xumu
Highly enantioselective Ir/f-amphox-catalyzed hydrogenation of ketoamides: efficient access to chiral hydroxy amides
Organic Chemistry Frontiers, 2018, 5, 2000
1554305 CIFC32 H7 Cl4 F10 N3 O2P 1 21/m 16.4792; 25.1943; 10.1094
90; 106.673; 90		1580.87Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long
The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence
Organic Chemistry Frontiers, 2018, 5, 1877
1554306 CIFC36 H11 Cl2 F10 N5 O2.5P 1 21/m 16.3689; 19.2075; 14.4005
90; 96.153; 90		1751.5Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long
The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence
Organic Chemistry Frontiers, 2018, 5, 1877
1554307 CIFC38 H7 Br2 F10 N5 O3P n m a18.5573; 18.3335; 14.8419
90; 90; 90		5049.5Wang, Jun-Fei; Yao, Yuhang; Ning, Yingying; Meng, Yin-Shan; Hou, Chun-Liang; Zhang, Jing; Zhang, Jun-Long
The design of rigid cyclic tripyrrins: the importance of intermolecular interactions on aggregation and luminescence
Organic Chemistry Frontiers, 2018, 5, 1877
1554308 CIFC28 H26 F N O8 SP b c a8.2423; 18.2962; 34.5544
90; 90; 90		5210.9Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng
Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction
Organic Chemistry Frontiers, 2018, 5, 1950
1554309 CIFC28.8 H27.6 N2 O10 SP 1 21/c 121.4204; 21.5628; 14.5587
90; 97.091; 90		6673Xing, Siyang; Cui, Hong; Qin, Jiajing; Gu, Nan; Zhang, Bowei; Wang, Kui; Wang, Ying; Xia, Li; Wang, Yumeng
Diastereoselective synthesis of cis-1,3-disubstituted isoindolines via a highly site-selective tandem cyclization reaction
Organic Chemistry Frontiers, 2018, 5, 1950
1554310 CIFC17 H14 O2P 1 21/c 110.5915; 15.1258; 9.0257
90; 109.468; 90		1363.29Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming
2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols
Organic Chemistry Frontiers, 2018, 5, 1900
1554311 CIFC15 H18 O2P -15.6491; 11.5037; 11.5175
111.795; 99.48; 90.087		683.87Zheng, Wei-Feng; Zhang, Wanli; Huang, Jianhao; Yu, Yibo; Qian, Hui; Ma, Shengming
2,3-Allenoic acids via palladium-catalyzed carboxylation of propargylic alcohols
Organic Chemistry Frontiers, 2018, 5, 1900
1554312 CIFC16 H17 Br O4P 1 21 110.573; 7.311; 11.35
90; 115.216; 90		793.7Li, Sujia; Lv, Jian; Luo, Sanzhong
Enantioselective indium(i)-catalyzed [4 + 2] annulation of alkoxyallenes and β,γ-unsaturated α-keto esters
Organic Chemistry Frontiers, 2018, 5, 1787
1554313 CIFC20 H18 N4 O2P -18.46; 9.59; 11.8
97.55; 104.24; 108.51		857Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata
Metal-free direct oxidative C‒C bond coupling of pyrazolones and quinoxalinones
Organic Chemistry Frontiers, 2018, 5, 1928
1554314 CIFC15 H16 N4 O2P 1 21/n 19.998; 9.281; 14.416
90; 95.77; 90		1330.9Toonchue, Saowanee; Sumunnee, Ladawan; Phomphrai, Khamphee; Yotphan, Sirilata
Metal-free direct oxidative C‒C bond coupling of pyrazolones and quinoxalinones
Organic Chemistry Frontiers, 2018, 5, 1928
1554315 CIFC20 H40.5 O3.25 SiP 1 21 17.3563; 46.699; 12.909
90; 92.798; 90		4429.4Santalla, Hugo; Garrido, Fátima; Gómez, Generosa; Fall, Yagamare
A more reliable synthesis of a Gemini vitamin D analog, a potentially effective chemotherapeutic agent for the treatment of colorectal carcinomas
Organic Chemistry Frontiers, 2018, 5, 2016
1554316 CIFC32 H31 N O5P 21 21 2110.1535; 10.5316; 25.565
90; 90; 90		2733.73Duan, Chuan-Qi; He, Xiao-Long; Du, Wei; Chen, Ying-Chun
Asymmetric [4 + 2] cycloadditions with 3-furfural derivatives and α-cyano-α,β-unsaturated ketones
Organic Chemistry Frontiers, 2018, 5, 2057
1554317 CIFC23 H20 Br N O2 SP -110.0726; 10.735; 19.604
82.045; 86.428; 81.212		2072.9Jiang, Bo; Wei, Yin; Shi, Min
Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2091
1554318 CIFC26 H23 N O2 SP -19.447; 10.559; 12.512
76.431; 77.755; 64.585		1087Jiang, Bo; Wei, Yin; Shi, Min
Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2091
1554319 CIFC26 H23 N O2 SP 1 21/n 111.7526; 13.4984; 13.5265
90; 92.44; 90		2143.9Jiang, Bo; Wei, Yin; Shi, Min
Gold- and silver-catalyzed intramolecular annulation and rearrangement of aniline-linked 1,6-enynes containing methylenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2091
1554320 CIFC38 H28 N2 O3 SP 21 21 219.00774; 11.44511; 29.0288
90; 90; 90		2992.71Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming
Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives
Organic Chemistry Frontiers, 2018, 5, 2126
1554321 CIFC38 H28 N2 O4 SC 1 2 114.8962; 11.3205; 20.153
90; 102.279; 90		3320.7Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming
Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives
Organic Chemistry Frontiers, 2018, 5, 2126
1554322 CIFC26 H21 N O4 SP 1 21 16.3467; 16.1435; 10.7987
90; 96.301; 90		1099.73Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming
Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives
Organic Chemistry Frontiers, 2018, 5, 2126
1554323 CIFC30 H22 Cl N O2 SP 1 21 110.4185; 15.4927; 15.8277
90; 95.756; 90		2541.9Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming
Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives
Organic Chemistry Frontiers, 2018, 5, 2126
1554324 CIFC31 H56 F6 Mg N4 O14 S2P 19.2007; 9.2791; 14.237
97.598; 91.193; 97.349		1194.02Zhang, Xiying; Liu, Xiaohua; Zhang, Jianlin; Zhang, Dong; Lin, Lili; Feng, Xiaoming
Enantioselective [3 + 2] cycloaddition and rearrangement of thiazolium salts to synthesize thiazole and 1,4-thiazine derivatives
Organic Chemistry Frontiers, 2018, 5, 2126
1554325 CIFC25 H19 N3 OP -18.2339; 14.7918; 17.1794
101.33; 95.203; 106.126		1947.28Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu
A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines
Organic Chemistry Frontiers, 2018, 5, 2303
1554326 CIFC25 H16 F3 N3 O2P 1 21/c 119.5242; 8.4475; 25.582
90; 107.178; 90		4031.04Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu
A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines
Organic Chemistry Frontiers, 2018, 5, 2303
1554327 CIFC26 H21 F2 N3I 41/a :218.7671; 18.7671; 24.2076
90; 90; 90		8526.01Liu, Yun-Lin; Mao, Xiang-Yu; Lin, Xiao-Tong; Chen, Guo-Shu
A Zn(OTf)2 catalyzed Ugi-type reaction of 3-(2-isocyanoethyl)indoles with indole-derived ketimines: rapid access to hexacyclic spiroindolines
Organic Chemistry Frontiers, 2018, 5, 2303
1554328 CIFC16 H15 Cl OP b c n57.5837; 5.8021; 8.0527
90; 90; 90		2690.46Chen, Mintao; Wei, Yin; Shi, Min
A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2030
1554329 CIFC12 H13 F3 O2 SP -110.0641; 10.4692; 12.4244
90.033; 93.737; 96.649		1297.46Chen, Mintao; Wei, Yin; Shi, Min
A facile method for the synthesis of trifluoromethylthio-/chloro-homoallylic alcohols from methylenecyclopropanes
Organic Chemistry Frontiers, 2018, 5, 2030
1554330 CIFC66 H78 O2P -112.134; 13.857; 17.116
70.214; 75.507; 73.496		2558.3Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.
Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation
Organic Chemistry Frontiers, 2018, 5, 2288
1554331 CIFC68 H74P -19.3311; 9.8219; 16.1042
103.794; 94.992; 112.566		1297.14Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.
Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation
Organic Chemistry Frontiers, 2018, 5, 2288
1554332 CIFC95.5 H118 Cl4.5 O4.93P 1 21 115.3329; 18.3488; 15.6332
90; 99.6319; 90		4336.2Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.
Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation
Organic Chemistry Frontiers, 2018, 5, 2288
1554333 CIFC127.75 H123 O1.75C 1 2/c 132.048; 25.4121; 26.3829
90; 102.865; 90		20947Yang, Wenlong; Kazemi, Rezvan R.; Karunathilake, Nelum; Catalano, Vincent J.; Alpuche-Aviles, Mario A.; Chalifoux, Wesley A.
Expanding the scope of peropyrenes and teropyrenes through a facile InCl3-catalyzed multifold alkyne benzannulation
Organic Chemistry Frontiers, 2018, 5, 2288
1554334 CIFC11 H10 Cl0.07 Fe N OP 21 21 219.5467; 13.5703; 26.06
90; 90; 90		3376.1Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu
Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone‒ferrocene hybrids as novel RalA inhibitors
Organic Chemistry Frontiers, 2018, 5, 2229
1554335 CIFC34 H35 Cl2 Fe N3 O4P 41 21 212.0535; 12.0535; 43.8649
90; 90; 90		6373Zhang, Yuehua; Wang, Chunting; Huang, Wei; Haruehanroengra, Phensinee; Peng, Cheng; Sheng, Jia; Han, Bo; He, Gu
Application of organocatalysis in bioorganometallic chemistry: asymmetric synthesis of multifunctionalized spirocyclic pyrazolone‒ferrocene hybrids as novel RalA inhibitors
Organic Chemistry Frontiers, 2018, 5, 2229
1554336 CIFC20.57 H26.27 Cl N O3.57C 1 2 118.4603; 16.6736; 13.8087
90; 103.239; 90		4137.4Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.
Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines
Organic Chemistry Frontiers, 2018, 5, 2171
1554337 CIFC20 H24 Cl N O3P -111.4568; 11.4834; 14.2866
94.508; 106.183; 90.764		1798.31Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.
Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines
Organic Chemistry Frontiers, 2018, 5, 2171
1554338 CIFC20 H25 N O4P 1 21/c 117.0841; 18.7193; 11.1858
90; 100.62; 90		3516Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.
Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines
Organic Chemistry Frontiers, 2018, 5, 2171
1554339 CIFC20 H24 Cl N O5P 1 21/n 111.3027; 7.2512; 23.102
90; 98.784; 90		1871.19Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.
Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines
Organic Chemistry Frontiers, 2018, 5, 2171
1554340 CIFC20 H24 Cl N O3P 21 21 217.508; 11.2397; 21.9828
90; 90; 90		1855.08Olivon, F.; Apel, C.; Retailleau, P.; Allard, P. M.; Wolfender, J. L.; Touboul, D.; Roussi, F.; Litaudon, M.; Desrat, S.
Searching for original natural products by molecular networking: detection, isolation and total synthesis of chloroaustralasines
Organic Chemistry Frontiers, 2018, 5, 2171

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