Crystallography Open Database

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1508841 CIFC26 H24P 1 21/c 111.406; 5.8201; 15.187
90; 95.53; 90		1003.5Jiang, Huanfeng; Gao, Yang; Wu, Wanqing; Huang, Yubing
Pd(II)-Catalyzed Highly Regio- and Stereoselective Assembly of C-C Double Bonds: An Efficient Method for the Synthesis of 2,4-Dihalo-1,3,5-trienes from Alkynols.
Organic letters, 2013, 15, 238-241
1508842 CIFC17 H14 Br N OP 21 21 216.1191; 12.656; 18.088
90; 90; 90		1400.8Cao, Zhong-Yan; Zhou, Feng; Yu, Yi-Hua; Zhou, Jian
A Highly Diastereo- and Enantioselective Hg(II)-Catalyzed Cyclopropanation of Diazooxindoles and Alkenes.
Organic letters, 2013, 15, 42-45
1508843 CIFC22 H31 N O2P 1 21 17.6187; 15.2421; 8.3982
90; 99.42; 90		962.09Martin, Rhia M.; Bergman, Robert G.; Ellman, Jonathan A.
Synthesis of Isoquinuclidines from Highly Substituted Dihydropyridines via the Diels-Alder Reaction.
Organic letters, 2013, 15, 444-447
1508844 CIFC15 H18 O4P 1 21/c 115.5908; 12.0381; 7.2191
90; 99.952; 90		1334.52Song, Liyan; Yao, Hongliang; Zhu, Liangyu; Tong, Rongbiao
Asymmetric Total Syntheses of (-)-Penicipyrone and (-)-Tenuipyrone via Biomimetic Cascade Intermolecular Michael Addition/Cycloketalization.
Organic letters, 2013, 15, 6-9
1508845 CIFC13 H16 O4P 1 21/c 110.6914; 9.8462; 11.5299
90; 110.216; 90		1138.98Song, Liyan; Yao, Hongliang; Zhu, Liangyu; Tong, Rongbiao
Asymmetric Total Syntheses of (-)-Penicipyrone and (-)-Tenuipyrone via Biomimetic Cascade Intermolecular Michael Addition/Cycloketalization.
Organic letters, 2013, 15, 6-9
1508846 CIFC12.5 H20 Cl2 Ir N O2P 21 21 2112.8975; 14.6754; 16.4298
90; 90; 90		3109.8Wetzel, Alexander; Wöckel, Simone; Schelwies, Mathias; Brinks, Marion K.; Rominger, Frank; Hofmann, Peter; Limbach, Michael
Selective Alkylation of Amines with Alcohols by Cp*-Iridium(III) Half-Sandwich Complexes.
Organic letters, 2013, 15, 266-269
1508847 CIFC18 H23 N O3P -16.7576; 9.8259; 13.085
92.213; 97.254; 92.098		860.49Wang, Gang; Liu, Xiaohua; Huang, Tianyu; Kuang, Yulong; Lin, Lili; Feng, Xiaoming
Asymmetric catalytic 1,3-dipolar cycloaddition reaction of nitrile imines for the synthesis of chiral spiro-pyrazoline-oxindoles.
Organic letters, 2013, 15, 76-79
1508848 CIFC33 H29 N3 O3P 1 21 112.016; 18.7857; 12.339
90; 97.777; 90		2759.7Wang, Gang; Liu, Xiaohua; Huang, Tianyu; Kuang, Yulong; Lin, Lili; Feng, Xiaoming
Asymmetric catalytic 1,3-dipolar cycloaddition reaction of nitrile imines for the synthesis of chiral spiro-pyrazoline-oxindoles.
Organic letters, 2013, 15, 76-79
1508849 CIFC29 H31 N3 O3 SP 21 21 219.0374; 15.0633; 19.6158
90; 90; 90		2670.4Wang, Gang; Liu, Xiaohua; Huang, Tianyu; Kuang, Yulong; Lin, Lili; Feng, Xiaoming
Asymmetric catalytic 1,3-dipolar cycloaddition reaction of nitrile imines for the synthesis of chiral spiro-pyrazoline-oxindoles.
Organic letters, 2013, 15, 76-79
1508850 CIFC36 H48 S4 Si2P 1 21/c 114.45; 16.149; 16.146
90; 110.285; 90		3534Dou, Chuandong; Saito, Shohei; Gao, Libin; Matsumoto, Naoki; Karasawa, Takashi; Zhang, Hongyu; Fukazawa, Aiko; Yamaguchi, Shigehiro
Sequential Electrophilic and Photochemical Cyclizations from Bis(bithienyl)acetylene to a Tetrathienonaphthalene Core.
Organic letters, 2013, 15, 80-83
1508851 CIFC36 H48 S4 Si2P -17.5456; 12.1175; 19.49
80.956; 88.114; 87.511		1757.6Dou, Chuandong; Saito, Shohei; Gao, Libin; Matsumoto, Naoki; Karasawa, Takashi; Zhang, Hongyu; Fukazawa, Aiko; Yamaguchi, Shigehiro
Sequential Electrophilic and Photochemical Cyclizations from Bis(bithienyl)acetylene to a Tetrathienonaphthalene Core.
Organic letters, 2013, 15, 80-83
1508852 CIFC36 H49 I S4 Si2P -18.5863; 12.175; 18.897
92.036; 96.456; 98.521		1938.5Dou, Chuandong; Saito, Shohei; Gao, Libin; Matsumoto, Naoki; Karasawa, Takashi; Zhang, Hongyu; Fukazawa, Aiko; Yamaguchi, Shigehiro
Sequential Electrophilic and Photochemical Cyclizations from Bis(bithienyl)acetylene to a Tetrathienonaphthalene Core.
Organic letters, 2013, 15, 80-83
1508853 CIFC52 H30 F6 SP -111.2017; 12.1697; 15.1195
85.32; 82.624; 72.927		1951.88Li, Jing; Huang, Huanan; Liang, Weihong; Gao, Qun; Duan, Zheng
Catalytic C-h and C-s bond activation of thiophenes.
Organic letters, 2013, 15, 282-285
1508854 CIFC69 H52 SP -110.4792; 13.4657; 20.0797
70.764; 77.704; 82.037		2606.7Li, Jing; Huang, Huanan; Liang, Weihong; Gao, Qun; Duan, Zheng
Catalytic C-h and C-s bond activation of thiophenes.
Organic letters, 2013, 15, 282-285
1508855 CIFC44 H35 F4 SP 1 21/c 19.3242; 20.5863; 20.4716
90; 92.4025; 90		3926.09Li, Jing; Huang, Huanan; Liang, Weihong; Gao, Qun; Duan, Zheng
Catalytic C-h and C-s bond activation of thiophenes.
Organic letters, 2013, 15, 282-285
1508856 CIFC213 H201 S4P -116.0668; 16.7268; 18.1635
96.294; 99.037; 108.324		4510Li, Jing; Huang, Huanan; Liang, Weihong; Gao, Qun; Duan, Zheng
Catalytic C-h and C-s bond activation of thiophenes.
Organic letters, 2013, 15, 282-285
1508857 CIFC32 H29 Cl N2 O3P 21 21 218.3771; 10.29; 31.168
90; 90; 90		2686.69Shi, Feng; Xing, Gui-Juan; Zhu, Ren-Yi; Tan, Wei; Tu, Shujiang
A Catalytic Asymmetric Isatin-Involved Povarov Reaction: Diastereo- and Enantioselective Construction of Spiro[indolin-3,2'-quinoline] Scaffold.
Organic letters, 2013, 15, 128-131
1508858 CIFC28 H25 N O4P 1 21 112.652; 5.3373; 17.942
90; 109.082; 90		1145Wu, Hua; He, Yu-Ping; Gong, Liu-Zhu
Direct Access to Enantioenriched Spiroacetals through Asymmetric Relay Catalytic Three-Component Reaction.
Organic letters, 2013, 15, 460-463
1508859 CIFC15 H19 N O3P -16.9397; 8.8694; 11.1168
97.572; 94.165; 92.775		675.33Reddy, B. V. Subba; Reddy, M. Ramana; Rao, Y. Gopal; Yadav, J. S.; Sridhar, B.
Cu(OTf)(2)-Catalyzed Synthesis of 2,3-Disubstituted Indoles and 2,4,5-Trisubstituted Pyrroles from α-Diazoketones.
Organic letters, 2013, 15, 464-467
1508860 CIFC14 H15 N O2P 1 21/n 111.7298; 9.2723; 11.8853
90; 103.883; 90		1254.91Reddy, B. V. Subba; Reddy, M. Ramana; Rao, Y. Gopal; Yadav, J. S.; Sridhar, B.
Cu(OTf)(2)-Catalyzed Synthesis of 2,3-Disubstituted Indoles and 2,4,5-Trisubstituted Pyrroles from α-Diazoketones.
Organic letters, 2013, 15, 464-467
1508861 CIFC34 H32 N4P 1 21/c 113.046; 18.896; 21.809
90; 91.007; 90		5375Chandra, Brijesh; Mahanta, Sanjeev P.; Pati, Narendra N.; Baskaran, Sambath; Kanaparthi, Ravi K.; Sivasankar, Chinnappan; Panda, Pradeepta K.
Calix[2]bispyrrolylarenes: New Expanded Calix[4]pyrroles for Fluorometric Sensing of Anions via Extended π-Conjugation.
Organic letters, 2013, 15, 306-309
1508862 CIFC24 H16 N2P 1 21 17.6144; 7.5543; 29.9948
90; 91.624; 90		1724.65Louillat, Marie-Laure; Patureau, Frederic W.
Toward polynuclear ru-cu catalytic dehydrogenative C-N bond formation, on the reactivity of carbazoles.
Organic letters, 2013, 15, 164-167
1508863 CIFC24 H24 O4P -19.2295; 10.3951; 11.3783
86.591; 69.851; 79.622		1008.07Qin, Changming; Davies, Huw M. L.
Enantioselective Synthesis of 2-Arylbicyclo[1.1.0]butane Carboxylates.
Organic letters, 2013, 15, 310-313
1508864 CIFC25 H25 N3 O3C 1 2 121.033; 9.9868; 10.2026
90; 102.928; 90		2088.8Hong, Bor-Cherng; Liao, Wei-Kai; Dange, Nitin S.; Liao, Ju-Hsiou
One-pot organocatalytic enantioselective domino double-Michael reaction and pictet-spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers.
Organic letters, 2013, 15, 468-471
1508865 CIFC25 H24 Cl N3 O3P 21 21 218.1146; 9.2164; 35.493
90; 90; 90		2654.4Hong, Bor-Cherng; Liao, Wei-Kai; Dange, Nitin S.; Liao, Ju-Hsiou
One-pot organocatalytic enantioselective domino double-Michael reaction and pictet-spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers.
Organic letters, 2013, 15, 468-471
1508866 CIFC12 H18 F6 N2 O2P 1 2/c 19.4219; 8.6467; 18.7345
90; 103.222; 90		1485.81Riofski, Mark V.; Hart, Allison D.; Colby, David A.
Amidinate salt of hexafluoroacetone hydrate for the preparation of fluorinated compounds by the release of trifluoroacetate.
Organic letters, 2013, 15, 208-211
1508867 CIFC25 H28 Cl N O6P 1 21/n 113.871; 11.664; 15.1202
90; 92.72; 90		2443.6Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L.
Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.
Organic letters, 2013, 15, 350-353
1508868 CIFC29 H29 N O6P 1 21/c 19.4038; 10.7199; 24.4225
90; 99.093; 90		2431.04Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L.
Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.
Organic letters, 2013, 15, 350-353
1508869 CIFC29 H29 N O6P -111.3123; 13.5731; 16.6509
78.645; 73.569; 86.82		2404.2Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L.
Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.
Organic letters, 2013, 15, 350-353
1508870 CIFC27 H33 N O7P b c a19.1983; 10.9762; 23.4467
90; 90; 90		4940.8Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L.
Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.
Organic letters, 2013, 15, 350-353
1508871 CIFC28 H33 N O7P -19.6224; 10.0813; 14.8728
103.357; 105.497; 103.944		1280.26Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L.
Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.
Organic letters, 2013, 15, 350-353
1508872 CIFC30 H44 S4 Si4P 1 21/n 110.779; 6.217; 27.444
90; 93; 90		1836.6Wu, Tianjing; Shi, Jianwu; Li, Chunli; Song, Jinsheng; Xu, Li; Wang, Hua
Synthesis of Dendrimers Based on Tetrakis(thiophene-2-yl)ethene as New Dendron.
Organic letters, 2013, 15, 354-357
1508873 CIFC110 H140 S16 Si12P -112.183; 16.129; 16.62
100.265; 92.579; 90.124		3210Wu, Tianjing; Shi, Jianwu; Li, Chunli; Song, Jinsheng; Xu, Li; Wang, Hua
Synthesis of Dendrimers Based on Tetrakis(thiophene-2-yl)ethene as New Dendron.
Organic letters, 2013, 15, 354-357
1508874 CIFC27 H22 N2P -18.3493; 10.2504; 13.0418
91.274; 104.819; 112.131		990.74Chen, Hui; Sanjaya, Stephen; Wang, Yi-Feng; Chiba, Shunsuke
Copper-catalyzed aliphatic C-h amination with an amidine moiety.
Organic letters, 2013, 15, 212-215
1508875 CIFC25 H20 N2P 1 21/c 112.2998; 8.3428; 18.0813
90; 95.545; 90		1846.7Chen, Hui; Sanjaya, Stephen; Wang, Yi-Feng; Chiba, Shunsuke
Copper-catalyzed aliphatic C-h amination with an amidine moiety.
Organic letters, 2013, 15, 212-215
1508876 CIFC28 H24 Br N O3 SP 1 21 117.676; 5.727; 23.637
90; 92.756; 90		2390Guo, Qunsheng; Zhao, John Cong-Gui
Highly enantioselective three-component direct mannich reactions of unfunctionalized ketones catalyzed by bifunctional organocatalysts.
Organic letters, 2013, 15, 508-511
1508877 CIFC16 H12 N2 O3P -16.9631; 9.251; 11.149
82.052; 85.96; 68.329		660.9Zhu, Yan-Ping; Fei, Zhuan; Liu, Mei-Cai; Jia, Feng-Cheng; Wu, An-Xin
Direct One-Pot Synthesis of Luotonin F and Analogues via Rational Logical Design.
Organic letters, 2013, 15, 378-381
1508878 CIFC32 H30 O3 SiP -19.688; 10.4402; 12.9565
89.249; 80.806; 85.661		1289.9Kondo, Shin-Ichi; Bie, Yi; Yamamura, Masaki
Ratiometric Fluorescence Detection of Anions by Silanediol-based Receptors Bearing Anthryl and Pyrenyl Groups.
Organic letters, 2013, 15, 520-523
1508879 CIFC62 H70 F12 N7 O14 P2C 1 c 111.021; 22.8264; 26.376
90; 90.593; 90		6635Yan, Xuzhou; Li, Zhengtao; Wei, Peifa; Huang, Feihe
Chemically-Responsive Complexation of A Diquaternary Salt with Bis(m-phenylene)-32-Crown-10 Derivatives and Host Substituent Effect on Complexation Geometry.
Organic letters, 2013, 15, 534-537
1508880 CIFC69 H78 F12 Fe2 N2 O15 P2P n a 2121.8315; 10.7382; 29.5987
90; 90; 90		6938.9Yan, Xuzhou; Li, Zhengtao; Wei, Peifa; Huang, Feihe
Chemically-Responsive Complexation of A Diquaternary Salt with Bis(m-phenylene)-32-Crown-10 Derivatives and Host Substituent Effect on Complexation Geometry.
Organic letters, 2013, 15, 534-537
1508881 CIFC68 H82 F12 N4 O20 P2C 1 c 117.9964; 13.7356; 32.6891
90; 102.548; 90		7887.5Yan, Xuzhou; Li, Zhengtao; Wei, Peifa; Huang, Feihe
Chemically-Responsive Complexation of A Diquaternary Salt with Bis(m-phenylene)-32-Crown-10 Derivatives and Host Substituent Effect on Complexation Geometry.
Organic letters, 2013, 15, 534-537
1508882 CIFC24 H19 N O5 SP 15.737; 8.686; 10.931
83.072; 79.957; 75.074		516.6An, Jing; Lu, Liang-Qiu; Yang, Qing-Qing; Wang, Tao; Xiao, Wen-Jing
Enantioselective Construction of Oxa- and Aza-Angular Triquinanes through Tandem [4 + 1]/[3 + 2] Cycloaddition of Sulfur Ylides and Nitroolefins.
Organic letters, 2013, 15, 542-545
1508883 CIFC26 H21 N O5P 1 21/c 111.1729; 22.3738; 8.8833
90; 107.866; 90		2113.56An, Jing; Lu, Liang-Qiu; Yang, Qing-Qing; Wang, Tao; Xiao, Wen-Jing
Enantioselective Construction of Oxa- and Aza-Angular Triquinanes through Tandem [4 + 1]/[3 + 2] Cycloaddition of Sulfur Ylides and Nitroolefins.
Organic letters, 2013, 15, 542-545
1508884 CIFC16 H17 N O2 S2P b c a7.861; 9.93; 42.05
90; 90; 90		3282Xu, Xiao-Bo; Liu, Jian; Zhang, Jian-Jian; Wang, Ya-Wen; Peng, Yu
Nickel-mediated inter- and intramolecular C-s coupling of thiols and thioacetates with aryl iodides at room temperature.
Organic letters, 2013, 15, 550-553
1508885 CIFC13 H13 N O2 SP b c a8.132; 12.907; 23.129
90; 90; 90		2428Xu, Xiao-Bo; Liu, Jian; Zhang, Jian-Jian; Wang, Ya-Wen; Peng, Yu
Nickel-mediated inter- and intramolecular C-s coupling of thiols and thioacetates with aryl iodides at room temperature.
Organic letters, 2013, 15, 550-553
1508886 CIFC24 H32 N4 O4 SP 1 21 113.442; 6.2752; 16.172
90; 106.076; 90		1310.8Bian, Jianwei; Blakemore, David; Warmus, Joseph S.; Sun, Jianmin; Corbett, Matthew; Rose, Colin R.; Bechle, Bruce M.
Diastereoselective Synthesis of β-Heteroaryl syn-α-Methyl-β-Amino Acid Derivatives via a Double Chiral Auxiliary Approach.
Organic letters, 2013, 15, 562-565
1508887 CIFC21 H20 O5 SP -18.1107; 11.3209; 11.3866
108.914; 101.259; 104.447		913.25Reddy Chidipudi, Suresh; Wieczysty, Martin D.; Khan, Imtiaz; Lam, Hon Wai
Synthesis of Benzopyrans by Pd(II)- or Ru(II)-Catalyzed C-H Alkenylation of 2-Aryl-3-hydroxy-2-cyclohexenones.
Organic letters, 2013, 15, 570-573
1508888 CIFC40 H42 O8P 1 21/c 17.2612; 46.73; 9.8379
90; 104.021; 90		3238.7Lim, Hee Nam; Parker, Kathlyn A.
Total synthesis of kingianin a.
Organic letters, 2013, 15, 398-401
1508889 CIFC54 H62 N2 O4P -110.8252; 14.0413; 16.0269
80.5192; 80.3028; 76.9564		2318.87Masuda, Motoki; Maeda, Chihiro; Yoshioka, Naoki
Synthesis of Carbazole-Based Selenaporphyrin via Annulation.
Organic letters, 2013, 15, 578-581
1508890 CIFC50 H50 N2 Se2P -110.1478; 12.6951; 16.6983
90.204; 104.566; 111.507		1926.1Masuda, Motoki; Maeda, Chihiro; Yoshioka, Naoki
Synthesis of Carbazole-Based Selenaporphyrin via Annulation.
Organic letters, 2013, 15, 578-581
1508891 CIFC18 H26 N2 OP 21 21 216.385; 8.7697; 27.5194
90; 90; 90		1540.94Huang, Sheng-Dian; Zhang, Yu; Cao, Ming-Ming; Di, Ying-Tong; Tang, Gui-Hua; Peng, Zong-Gen; Jiang, Jian-Dong; He, Hong-Ping; Hao, Xiao-Jiang
Myriberine A, a New Alkaloid with an Unprecedented Heteropentacyclic Skeleton from Myrioneuron faberi.
Organic letters, 2013, 15, 590-593
1508892 CIFC25 H42 OP 21 21 216.214; 15.5633; 45.916
90; 90; 90		4440.6Chiba, Ryota; Minami, Atsushi; Gomi, Katsuya; Oikawa, Hideaki
Identification of Ophiobolin F Synthase by a Genome Mining Approach: A Sesterterpene Synthase from Aspergillus clavatus.
Organic letters, 2013, 15, 594-597
1508893 CIFC98 H156 F24 N22 Na4 O27 P4R 3 :H16.382; 16.382; 39.89
90; 90; 120		9271Izzo, Irene; Ianniello, Graziella; De Cola, Chiara; Nardone, Brunello; Erra, Loredana; Vaughan, Gavin; Tedesco, Consiglia; De Riccardis, Francesco
Structural effects of proline substitution and metal binding on hexameric cyclic peptoids.
Organic letters, 2013, 15, 598-601
1508894 CIFC30 H54 N6 O12P -18.3584; 9.1756; 11.6234
99.636; 101.488; 104.239		824.5Izzo, Irene; Ianniello, Graziella; De Cola, Chiara; Nardone, Brunello; Erra, Loredana; Vaughan, Gavin; Tedesco, Consiglia; De Riccardis, Francesco
Structural effects of proline substitution and metal binding on hexameric cyclic peptoids.
Organic letters, 2013, 15, 598-601
1508895 CIFC57 H49 Cl7 Fe N6 O6P -112.29; 14.996; 16.269
98.514; 106.348; 99.374		2778.6Zhou, Zaichun; Liu, Qiuhua; Yan, Ziqiang; Long, Ge; Zhang, Xi; Cao, Chenzhong; Jiang, Rongqing
Conversion of Electron Configuration of Iron Ion through Core Contraction of Porphyrin: Implications for Heme Distortion.
Organic letters, 2013, 15, 606-609
1508896 CIFC56 H48 Cl Fe N6 O6P 1 21/c 114.527; 30.638; 12.3382
90; 97.26; 90		5447.4Zhou, Zaichun; Liu, Qiuhua; Yan, Ziqiang; Long, Ge; Zhang, Xi; Cao, Chenzhong; Jiang, Rongqing
Conversion of Electron Configuration of Iron Ion through Core Contraction of Porphyrin: Implications for Heme Distortion.
Organic letters, 2013, 15, 606-609
1508897 CIFC57 H50 Cl Fe N6 O6P -115.923; 16.738; 22.371
91.302; 93.701; 90.604		5947.9Zhou, Zaichun; Liu, Qiuhua; Yan, Ziqiang; Long, Ge; Zhang, Xi; Cao, Chenzhong; Jiang, Rongqing
Conversion of Electron Configuration of Iron Ion through Core Contraction of Porphyrin: Implications for Heme Distortion.
Organic letters, 2013, 15, 606-609
1508898 CIFC58 H52 Cl Fe N6 O6P -115.749; 15.991; 16.15
61.74; 63.39; 62.81		3044.2Zhou, Zaichun; Liu, Qiuhua; Yan, Ziqiang; Long, Ge; Zhang, Xi; Cao, Chenzhong; Jiang, Rongqing
Conversion of Electron Configuration of Iron Ion through Core Contraction of Porphyrin: Implications for Heme Distortion.
Organic letters, 2013, 15, 606-609
1508899 CIFC59 H54 Cl Fe N6 O6P -114.0827; 16.3185; 16.6591
62.671; 75; 71.377		3194.3Zhou, Zaichun; Liu, Qiuhua; Yan, Ziqiang; Long, Ge; Zhang, Xi; Cao, Chenzhong; Jiang, Rongqing
Conversion of Electron Configuration of Iron Ion through Core Contraction of Porphyrin: Implications for Heme Distortion.
Organic letters, 2013, 15, 606-609
1508900 CIFC60 H56 Cl Fe N6 O6P -115.2; 16.065; 16.305
115.096; 116.65; 94.005		3051.7Zhou, Zaichun; Liu, Qiuhua; Yan, Ziqiang; Long, Ge; Zhang, Xi; Cao, Chenzhong; Jiang, Rongqing
Conversion of Electron Configuration of Iron Ion through Core Contraction of Porphyrin: Implications for Heme Distortion.
Organic letters, 2013, 15, 606-609
1508901 CIFC15 H14 N2 O2P 1 21/c 113.2153; 7.6831; 12.8817
90; 107.622; 90		1246.6Tran, Tuan P.; Mullins, Patrick B.; Am Ende, Christopher W.; Pettersson, Martin
Synthesis of Pyridopyrazine-1,6-diones from 6-Hydroxypicolinic Acids via a One-Pot Coupling/Cyclization Reaction.
Organic letters, 2013, 15, 642-645
1508902 CIFC12 H10 N4 OP b c a7.5741; 13.7438; 21.7946
90; 90; 90		2268.75Tran, Tuan P.; Mullins, Patrick B.; Am Ende, Christopher W.; Pettersson, Martin
Synthesis of Pyridopyrazine-1,6-diones from 6-Hydroxypicolinic Acids via a One-Pot Coupling/Cyclization Reaction.
Organic letters, 2013, 15, 642-645
1508903 CIFC16 H15 Br N2 O2P 1 21/c 115.8197; 12.6493; 7.2819
90; 95.363; 90		1450.79Tran, Tuan P.; Mullins, Patrick B.; Am Ende, Christopher W.; Pettersson, Martin
Synthesis of Pyridopyrazine-1,6-diones from 6-Hydroxypicolinic Acids via a One-Pot Coupling/Cyclization Reaction.
Organic letters, 2013, 15, 642-645
1508904 CIFC32 H31 N O7P 4310.3793; 10.3793; 25.352
90; 90; 90		2731.17Kim, U. Bin; Furkert, Daniel P.; Brimble, Margaret A.
Total synthesis of chaetoquadrins a-C.
Organic letters, 2013, 15, 658-661
1508905 CIFC16 H20 N2 Se Si2P 1 21/n 110.8314; 15.999; 12.6094
90; 115.323; 90		1975.1Lindner, Benjamin D.; Coombs, Benjamin A.; Schaffroth, Manuel; Engelhart, Jens U.; Tverskoy, Olena; Rominger, Frank; Hamburger, Manuel; Bunz, Uwe H. F.
From thia- to selenadiazoles: changing interaction priority.
Organic letters, 2013, 15, 666-669
1508906 CIFC26 H34 N2 Se Si2P 1 21/n 110.4163; 17.0453; 15.4541
90; 106.965; 90		2624.5Lindner, Benjamin D.; Coombs, Benjamin A.; Schaffroth, Manuel; Engelhart, Jens U.; Tverskoy, Olena; Rominger, Frank; Hamburger, Manuel; Bunz, Uwe H. F.
From thia- to selenadiazoles: changing interaction priority.
Organic letters, 2013, 15, 666-669
1508907 CIFC28 H44 N2 Se Si2P 1 21/n 114.751; 14.938; 15.035
90; 105.604; 90		3190.9Lindner, Benjamin D.; Coombs, Benjamin A.; Schaffroth, Manuel; Engelhart, Jens U.; Tverskoy, Olena; Rominger, Frank; Hamburger, Manuel; Bunz, Uwe H. F.
From thia- to selenadiazoles: changing interaction priority.
Organic letters, 2013, 15, 666-669
1508908 CIFC32 H46 N2 Se Si2P 1 21/n 114.8139; 15.1816; 30.2664
90; 93.844; 90		6791.6Lindner, Benjamin D.; Coombs, Benjamin A.; Schaffroth, Manuel; Engelhart, Jens U.; Tverskoy, Olena; Rominger, Frank; Hamburger, Manuel; Bunz, Uwe H. F.
From thia- to selenadiazoles: changing interaction priority.
Organic letters, 2013, 15, 666-669
1508909 CIFC36 H48 N2 Se Si2P -18.1957; 13.139; 17.152
78.547; 81.601; 80.832		1774.5Lindner, Benjamin D.; Coombs, Benjamin A.; Schaffroth, Manuel; Engelhart, Jens U.; Tverskoy, Olena; Rominger, Frank; Hamburger, Manuel; Bunz, Uwe H. F.
From thia- to selenadiazoles: changing interaction priority.
Organic letters, 2013, 15, 666-669
1508910 CIFC34 H46 N4 Se Si2P -19.0805; 12.4223; 16.7125
71.73; 83.493; 81.475		1765.88Lindner, Benjamin D.; Coombs, Benjamin A.; Schaffroth, Manuel; Engelhart, Jens U.; Tverskoy, Olena; Rominger, Frank; Hamburger, Manuel; Bunz, Uwe H. F.
From thia- to selenadiazoles: changing interaction priority.
Organic letters, 2013, 15, 666-669
1508911 CIFC36 H48 N2 S Si2P -18.2003; 13.1453; 17.1892
78.043; 81.532; 80.552		1775.8Lindner, Benjamin D.; Coombs, Benjamin A.; Schaffroth, Manuel; Engelhart, Jens U.; Tverskoy, Olena; Rominger, Frank; Hamburger, Manuel; Bunz, Uwe H. F.
From thia- to selenadiazoles: changing interaction priority.
Organic letters, 2013, 15, 666-669
1508912 CIFC22 H17 N3 O6P 1 21/n 110.9383; 9.6552; 19.32
90; 104.308; 90		1977.1Shu, Wen-Ming; Yang, Yan; Zhang, Dong-Xue; Wu, Liu-Ming; Zhu, Yan-Ping; Yin, Guo-Dong; Wu, An-Xin
Highly Efficient Synthesis of 3a,6a-Dihydrofuro[2,3-b]furans via a Novel Bicyclization.
Organic letters, 2013, 15, 456-459
1508913 CIFC22 H17 Br N2 O4P 1 21/n 110.877; 9.556; 19.596
90; 106.11; 90		1956.8Shu, Wen-Ming; Yang, Yan; Zhang, Dong-Xue; Wu, Liu-Ming; Zhu, Yan-Ping; Yin, Guo-Dong; Wu, An-Xin
Highly Efficient Synthesis of 3a,6a-Dihydrofuro[2,3-b]furans via a Novel Bicyclization.
Organic letters, 2013, 15, 456-459
1508914 CIFC22 H16 N2 O4P 1 21/n 110.8804; 5.4346; 31.653
90; 91.258; 90		1871.2Shu, Wen-Ming; Yang, Yan; Zhang, Dong-Xue; Wu, Liu-Ming; Zhu, Yan-Ping; Yin, Guo-Dong; Wu, An-Xin
Highly Efficient Synthesis of 3a,6a-Dihydrofuro[2,3-b]furans via a Novel Bicyclization.
Organic letters, 2013, 15, 456-459
1508915 CIFC38 H44 N2 O8 SP 110.54; 13.2962; 13.7619
71.577; 89.697; 69.957		1707.4Rajapaksa, Naomi S.; McGowan, Meredeth A.; Rienzo, Matthew; Jacobsen, Eric N.
Enantioselective total synthesis of (+)-reserpine.
Organic letters, 2013, 15, 706-709
1508925 CIFC22 H30 O6 SP 21 21 218.4382; 10.6416; 23.583
90; 90; 90		2117.7Saha, Mrinmoy; Carter, Rich G.
Toward a unified approach for the lycopodines: synthesis of 10-hydroxylycopodine, deacetylpaniculine, and paniculine.
Organic letters, 2013, 15, 736-739
1508926 CIFC19 H24 O5 SP 21 21 218.0743; 10.233; 20.798
90; 90; 90		1718.4Saha, Mrinmoy; Carter, Rich G.
Toward a unified approach for the lycopodines: synthesis of 10-hydroxylycopodine, deacetylpaniculine, and paniculine.
Organic letters, 2013, 15, 736-739
1508927 CIFC19 H26 O6 SP 21 21 218.0553; 10.1921; 21.862
90; 90; 90		1794.9Saha, Mrinmoy; Carter, Rich G.
Toward a unified approach for the lycopodines: synthesis of 10-hydroxylycopodine, deacetylpaniculine, and paniculine.
Organic letters, 2013, 15, 736-739
1508928 CIFC32 H28 N4 O8P 1 21/c 17.0625; 10.8486; 18.2963
90; 94.908; 90		1396.69Bhattacharya, Suman; Stojaković, Jelena; Saha, Binoy K.; Macgillivray, Leonard R.
A product of a templated solid-state photodimerization acts as a template: single-crystal reactivity in a single polymorph of a cocrystal.
Organic letters, 2013, 15, 744-747
1508929 CIFC32 H28 N4 O8P -17.3377; 11.3673; 18.0101
74.38; 90.072; 70.386		1355.82Bhattacharya, Suman; Stojaković, Jelena; Saha, Binoy K.; Macgillivray, Leonard R.
A product of a templated solid-state photodimerization acts as a template: single-crystal reactivity in a single polymorph of a cocrystal.
Organic letters, 2013, 15, 744-747
1508930 CIFC32 H28 N4 O8P -19.131; 11.006; 15.272
99.5; 98.7; 110.13		1384.9Bhattacharya, Suman; Stojaković, Jelena; Saha, Binoy K.; Macgillivray, Leonard R.
A product of a templated solid-state photodimerization acts as a template: single-crystal reactivity in a single polymorph of a cocrystal.
Organic letters, 2013, 15, 744-747
1508931 CIFC21 H13 Cl4 N2 O3C 1 2 126.5331; 8.0048; 9.7571
90; 97.575; 90		2054.25Alvarez-Mico, Xavier; Jensen, Paul R.; Fenical, William; Hughes, Chambers C.
Chlorizidine, a Cytotoxic 5H-Pyrrolo[2,1-a]isoindol-5-one-Containing Alkaloid from a Marine Streptomyces sp.
Organic letters, 2013, 15, 988-991
1508932 CIFC22 H14 Cl4 N2 O5P 17.649; 11.8911; 12.6157
105.779; 98.658; 92.067		1088.06Alvarez-Mico, Xavier; Jensen, Paul R.; Fenical, William; Hughes, Chambers C.
Chlorizidine, a Cytotoxic 5H-Pyrrolo[2,1-a]isoindol-5-one-Containing Alkaloid from a Marine Streptomyces sp.
Organic letters, 2013, 15, 988-991
1508933 CIFC9 H12 N2 O4P 1 21/c 17.7215; 7.90305; 16.5104
90; 101.898; 90		985.87Orimoto, Kohei; Oyama, Harufumi; Namera, Yuki; Niwa, Takashi; Nakada, Masahisa
Catalytic Asymmetric [4 + 2] Cycloadditions and Hosomi-Sakurai Reactions of α-Alkylidene β-Keto Imides.
Organic letters, 2013, 15, 768-771
1508934 CIFC18 H15 N O2P 1 21/c 116.6508; 12.0775; 14.6164
90; 109.539; 90		2770.1Liu, Xu; Zhang, Qian; Zhang, Dingyuan; Xin, Xiaoqing; Zhang, Rui; Zhou, Fenguo; Dong, Dewen
PPA-Mediated C-C Bond Formation: A Synthetic Route to Substituted Indeno[2,1-c]quinolin-6(7H)-ones.
Organic letters, 2013, 15, 776-779
1508935 CIFC28 H34 O10 SP 1 21 15.3516; 19.434; 13.261
90; 95.518; 90		1372.8Chooi, Yit-Heng; Fang, Jinxu; Liu, Hong; Filler, Scott G.; Wang, Pin; Tang, Yi
Genome Mining of a Prenylated and Immunosuppressive Polyketide from Pathogenic Fungi.
Organic letters, 2013, 15, 780-783
1508936 CIFC32 H34 O7P 21 21 2111.84571; 13.0433; 17.6965
90; 90; 90		2734.24Liu, Ming-Li; Duan, Ying-Hui; Hou, Yun-Long; Li, Chang; Gao, Hao; Dai, Yi; Yao, Xin-Sheng
Nardoaristolones A and B, Two Terpenoids with Unusual Skeletons from Nardostachys chinensis Batal.
Organic letters, 2013, 15, 1000-1003
1508937 CIFC14 H18 O2P 21 21 218.06899; 9.64395; 15.6052
90; 90; 90		1214.35Liu, Ming-Li; Duan, Ying-Hui; Hou, Yun-Long; Li, Chang; Gao, Hao; Dai, Yi; Yao, Xin-Sheng
Nardoaristolones A and B, Two Terpenoids with Unusual Skeletons from Nardostachys chinensis Batal.
Organic letters, 2013, 15, 1000-1003
1508938 CIFC20 H23 O3 PP 21 21 218.10822; 13.8133; 15.9269
90; 90; 90		1783.83Sawada, Takashi; Nakada, Masahisa
Enantioselective Total Synthesis of (+)-Colletoic Acid via Catalytic Asymmetric Intramolecular Cyclopropanation of an α-Diazo-β-keto Diphenylphosphine Oxide.
Organic letters, 2013, 15, 1004-1007
1508939 CIFC17 H36 N2 O2 S SiP 21 21 2110.963; 11.569; 17.41
90; 90; 90		2208.1Cornwall, Richard G.; Zhao, Baoguo; Shi, Yian
Catalytic asymmetric synthesis of cyclic sulfamides from conjugated dienes.
Organic letters, 2013, 15, 796-799
1508940 CIFC19 H12 Br2 O2P -17.0896; 9.732; 11.0373
99.588; 91.694; 96.224		745.58Zöphel, Lukas; Enkelmann, Volker; Müllen, Klaus
Tuning the HOMO-LUMO Gap of Pyrene Effectively via Donor-Acceptor Substitution: Positions 4,5 Versus 9,10.
Organic letters, 2013, 15, 804-807
1508941 CIFC20 H12 N2 O2P -17.0844; 10.1531; 10.6861
105.788; 98.355; 96.968		721.27Zöphel, Lukas; Enkelmann, Volker; Müllen, Klaus
Tuning the HOMO-LUMO Gap of Pyrene Effectively via Donor-Acceptor Substitution: Positions 4,5 Versus 9,10.
Organic letters, 2013, 15, 804-807
1508942 CIFC21 H12 N2 O2P m c n6.8305; 11.0589; 19.8828
90; 90; 90		1501.9Zöphel, Lukas; Enkelmann, Volker; Müllen, Klaus
Tuning the HOMO-LUMO Gap of Pyrene Effectively via Donor-Acceptor Substitution: Positions 4,5 Versus 9,10.
Organic letters, 2013, 15, 804-807
1508943 CIFC10 H9 O2C 1 2/c 115.5468; 10.7779; 10.234
90; 114.524; 90		1560.1Zöphel, Lukas; Enkelmann, Volker; Müllen, Klaus
Tuning the HOMO-LUMO Gap of Pyrene Effectively via Donor-Acceptor Substitution: Positions 4,5 Versus 9,10.
Organic letters, 2013, 15, 804-807
1508944 CIFC22 H18 O4P 1 21/a 111.3553; 7.1744; 11.5613
90; 119.414; 90		820.46Zöphel, Lukas; Enkelmann, Volker; Müllen, Klaus
Tuning the HOMO-LUMO Gap of Pyrene Effectively via Donor-Acceptor Substitution: Positions 4,5 Versus 9,10.
Organic letters, 2013, 15, 804-807
1508945 CIFC28 H22 N4P 1 21/n 19.0368; 9.2187; 13.518
90; 97.088; 90		1117.55Zöphel, Lukas; Enkelmann, Volker; Müllen, Klaus
Tuning the HOMO-LUMO Gap of Pyrene Effectively via Donor-Acceptor Substitution: Positions 4,5 Versus 9,10.
Organic letters, 2013, 15, 804-807
1508946 CIFC37 H25 N3 OP 1 21/c 117.131; 10.7442; 14.687
90; 93.702; 90		2697.6Ghosh, Avijit; Chatterjee, Tamal; Lee, Way-Zen; Ravikanth, Mangalampalli
Unusual formation of 21-oxacorrole from 21-oxaporphyrin induced by phosphoryl chloride.
Organic letters, 2013, 15, 1040-1043
1508947 CIFC19 H16 Cl N O3P 1 21/c 110.25; 10.486; 16.7877
90; 114.815; 90		1637.77Wei, Ying; Lin, Shaoxia; Liang, Fushun; Zhang, Jingping
N-Bromosuccinimide/1,8-Diazabicyclo[5.4.1]undec-7-ene Combination: β-Amination of Chalcones via a Tandem Bromoamination/Debromination Sequence.
Organic letters, 2013, 15, 852-855
1508948 CIFC19 H19 N OP 1 21/c 18.8897; 17.783; 10.6532
90; 112.329; 90		1557.8Nakai, Kenichiro; Kurahashi, Takuya; Matsubara, Seijiro
Synthesis of Quinolones by Nickel-Catalyzed Cycloaddition via Elimination of Nitrile.
Organic letters, 2013, 15, 856-859
1508949 CIFC20 H21 N OP 1 21/n 110.1765; 16.6581; 10.2059
90; 114.481; 90		1574.6Nakai, Kenichiro; Kurahashi, Takuya; Matsubara, Seijiro
Synthesis of Quinolones by Nickel-Catalyzed Cycloaddition via Elimination of Nitrile.
Organic letters, 2013, 15, 856-859

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