Crystallography Open Database

Result: there are 526796 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format

We are unable to provide that many records as a single archive.
You can instead download the entire COD archive as a single .zip, .tgz or .txz archive.

Displaying all data in COD

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 5268 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1506153 CIFC110 H86 N8 O ZnP -110.7956; 20.8712; 22.6826
91.146; 114.327; 89.589
4656.1Yen, Wei-Nan; Lo, Shang-Shih; Kuo, Ming-Cheng; Mai, Chi-Lun; Lee, Gene-Hsiang; Peng, Shie-Ming; Yeh, Chen-Yu
Synthesis, structure, and optical and electrochemical properties of star-shaped porphyrin-triarylamine conjugates.
Organic letters, 2006, 8, 4239-4242
1506154 CIFC27 H29 N O2 SiP 1 21 16.0952; 16.8339; 11.9653
90; 96.885; 90
1218.86Cho, Chang-Woo; Krische, Michael J.
Alpha-hydroxy esters via enantioselective hydrogen-mediated C-C coupling: regiocontrolled reactions of silyl-substituted 1,3-diynes.
Organic letters, 2006, 8, 3873-3876
1506155 CIFC15 H18 O4P 21 21 216.3696; 7.2069; 29.1029
90; 90; 90
1335.97Felzmann, Wolfgang; Arion, Vladimir B.; Mieusset, Jean-Luc; Mulzer, Johann
A tether controlled exo-selective trans-annular Diels-Alder (TADA) reaction.
Organic letters, 2006, 8, 3849-3851
1506156 CIFC16 H14 O3P 1 21/c 113.4544; 6.9898; 13.6325
90; 95.487; 90
1276.2Ye, Long-Wu; Sun, Xiu-Li; Zhu, Chun-Yin; Tang, Yong
Unexpected tandem ylide annulation reaction for controllable synthesis of 2H-chromenes and 4H-chromenes.
Organic letters, 2006, 8, 3853-3856
1506157 CIFC17 H14 N2 O5P 21 21 217.103; 13.709; 14.869
90; 90; 90
1447.9Das, Suven; Fröhlich, Roland; Pramanik, Animesh
Synthesis and fluorescent properties of a new class of heterocycles of isoindole fused imidazoles with phenolic subunits.
Organic letters, 2006, 8, 4263-4266
1506158 CIFC37 H32 N2 O7P 1 21/c 112.246; 23.6665; 11.8579
90; 113.398; 90
3154.05Johns, Deidre M.; Mori, Makoto; Williams, Robert M.
Synthetic studies on quinine: quinuclidine construction via a ketone enolate regio- and diastereoselective Pd-mediated allylic alkylation.
Organic letters, 2006, 8, 4051-4054
1506159 CIFC16 H19 N O4P 1 21/n 18.777; 13.634; 12.888
90; 109.04; 90
1457.9Li, Guo-You; Li, Bo-Gang; Yang, Tao; Liu, Guang-Ye; Zhang, Guo-Lin
Chaetoindicins A-C, three isoquinoline alkaloids from the fungus Chaetomium indicum.
Organic letters, 2006, 8, 3613-3615
1506160 CIFC18 H17 N O SP 1 21/c 15.6494; 20.1371; 13.3458
90; 93.685; 90
1515.11Majumdar, K. C.; Alam, S.
Regioselective unusual formation of spirocyclic 4-{2'-benzo(2',3'-dihydro)furo}- 9-methyl-2,3,9-trihydrothiopyrano[2,3-b]indole by 4-exo-trig aryl radical cyclization and rearrangement.
Organic letters, 2006, 8, 4059-4062
1506161 CIFC50 H64 O8C 1 2/c 126.437; 9.373; 19.0763
90; 105.419; 90
4556.9Masci, Bernardo; Levi Mortera, Stefano; Persiani, Daniela; Thuéry, Pierre
CsF-promoted acetyl dance at the narrow rim of p-tert-butyl[3.1.3.1]homooxacalixarene.
Organic letters, 2006, 8, 4405-4408
1506162 CIFC53 H70 O9P -111.2074; 13.3796; 16.7503
81.543; 77.386; 89.998
2423.1Masci, Bernardo; Levi Mortera, Stefano; Persiani, Daniela; Thuéry, Pierre
CsF-promoted acetyl dance at the narrow rim of p-tert-butyl[3.1.3.1]homooxacalixarene.
Organic letters, 2006, 8, 4405-4408
1506163 CIFC21 H20 O2P 1 21 19.214; 10.191; 9.606
90; 111.68; 90
838.2Kamikawa, Ken; Shimizu, Yasunori; Takemoto, Shin; Matsuzaka, Hiroyuki
Nickel-catalyzed [3+1+1] cycloaddition reactions of alkenyl Fischer carbene complexes with methylenecyclopropanes.
Organic letters, 2006, 8, 4011-4014
1506164 CIFC56 H50 Cl6 N4 O4 S2P 1 21/n 114.894; 25.242; 19.3
90; 110.11; 90
6814Kamikawa, Ken; Shimizu, Yasunori; Takemoto, Shin; Matsuzaka, Hiroyuki
Nickel-catalyzed [3+1+1] cycloaddition reactions of alkenyl Fischer carbene complexes with methylenecyclopropanes.
Organic letters, 2006, 8, 4011-4014
1506165 CIFC7 H20 B Na O9P 21 21 216.126; 7.3524; 29.508
90; 90; 90
1329.1Cammidge, Andrew N.; Goddard, Victoria H. M.; Gopee, Hemant; Harrison, Nicola L.; Hughes, David L.; Schubert, Christopher J.; Sutton, Benjamin M.; Watts, Gary L.; Whitehead, Andrew J.
Aryl trihydroxyborates: easily isolated discrete species convenient for direct application in coupling reactions.
Organic letters, 2006, 8, 4071-4074
1506166 CIFC17 H18 O6P 1 21/c 111.0011; 12.2123; 11.1592
90; 97.2768; 90
1487.1Song, Dong; McDonald, Robert; West, F. G.
Diastereoselective [4 + 4]-photocycloaddition reactions of pyran-2-ones: rapid access to functionalized 5-8-5 skeletons.
Organic letters, 2006, 8, 4075-4078
1506167 CIFC17 H20 O6P 1 21 16.0006; 8.0097; 14.4792
90; 90.68; 90
695.86Song, Dong; McDonald, Robert; West, F. G.
Diastereoselective [4 + 4]-photocycloaddition reactions of pyran-2-ones: rapid access to functionalized 5-8-5 skeletons.
Organic letters, 2006, 8, 4075-4078
1506168 CIFC23 H26 O6P 21 21 216.072; 15.035; 22.423
90; 90; 90
2047.1Xu, Gang; Hou, Ai-Jun; Wang, Rui-Rui; Liang, Guang-Yu; Zheng, Yong-Tang; Liu, Ze-Yuan; Li, Xiao-Li; Zhao, Yu; Huang, Sheng-Xiong; Peng, Li-Yan; Zhao, Qin-Shi
Przewalskin A: A new C23 terpenoid with a 6/6/7 carbon ring skeleton from Salvia przewalskii maxim.
Organic letters, 2006, 8, 4453-4456
1506169 CIFC26 H40 N2 O8 S2P -110.389; 11.02; 14.128
88.08; 73.29; 69.02
1442.1Mizobe, Yuji; Miyata, Mikiji; Hisaki, Ichiro; Hasegawa, Yasuchika; Tohnai, Norimitsu
Anomalous anthracene arrangement and rare excimer emission in the solid state: transcription and translation of molecular information.
Organic letters, 2006, 8, 4295-4298
1506170 CIFC13 H20 N O2.5 S1.5P -15.6042; 10.207; 14.106
74.48; 78.5; 75.38
744.74Mizobe, Yuji; Miyata, Mikiji; Hisaki, Ichiro; Hasegawa, Yasuchika; Tohnai, Norimitsu
Anomalous anthracene arrangement and rare excimer emission in the solid state: transcription and translation of molecular information.
Organic letters, 2006, 8, 4295-4298
1506171 CIFC14 H19 N O3 SP -15.554; 10.241; 13.571
76.31; 78.81; 75.28
717.9Mizobe, Yuji; Miyata, Mikiji; Hisaki, Ichiro; Hasegawa, Yasuchika; Tohnai, Norimitsu
Anomalous anthracene arrangement and rare excimer emission in the solid state: transcription and translation of molecular information.
Organic letters, 2006, 8, 4295-4298
1506172 CIFC13 H20 N2 O5 S2P -18.536; 9.6894; 10.5913
79.31; 68.379; 79.786
794.51Toumieux, Sylvestre; Compain, Philippe; Martin, Olivier R.; Selkti, Mohamed
New aspects of catalytic intramolecular C-H amination: unexpected formation of a seven-membered ring in nitrogen-containing systems.
Organic letters, 2006, 8, 4493-4496
1506173 CIFC16 H24 N2 O5 S2P 1 21/c 111.7943; 7.8523; 20.6581
90; 95.796; 90
1903.42Toumieux, Sylvestre; Compain, Philippe; Martin, Olivier R.; Selkti, Mohamed
New aspects of catalytic intramolecular C-H amination: unexpected formation of a seven-membered ring in nitrogen-containing systems.
Organic letters, 2006, 8, 4493-4496
1506174 CIFC13 H18 N2 O5 S2P 1 21/n 115.5689; 11.3899; 17.4891
90; 96.7179; 90
3080.02Toumieux, Sylvestre; Compain, Philippe; Martin, Olivier R.; Selkti, Mohamed
New aspects of catalytic intramolecular C-H amination: unexpected formation of a seven-membered ring in nitrogen-containing systems.
Organic letters, 2006, 8, 4493-4496
1506175 CIFC25 H42 O3 SiP 1 21/c 19.8222; 15.7753; 17.0784
90; 100.61; 90
2601Clark, Timothy B.; Woerpel, K. A.
Formation and reactivity of silacyclopropenes derived from siloxyalkynes: stereoselective formation of 1,2,4-triols.
Organic letters, 2006, 8, 4109-4112
1506176 CIFC20 H32 O3P -111.4318; 11.9829; 16.2499
70.808; 87.714; 80.765
2074.8Clark, Timothy B.; Woerpel, K. A.
Formation and reactivity of silacyclopropenes derived from siloxyalkynes: stereoselective formation of 1,2,4-triols.
Organic letters, 2006, 8, 4109-4112
1506177 CIFC10 H12 O4P 1 21/c 16.068; 10.6903; 14.2193
90; 92.64; 90
921.41Leyhane, Andrew J.; Snapper, Marc L.
Functionalized oxepines via fragmentation of highly strained epoxides.
Organic letters, 2006, 8, 5183-5186
1506178 CIFC14 H13 N2 O8P 1 21/n 110.7652; 5.778; 25.226
90; 96.903; 90
1557.7Leyhane, Andrew J.; Snapper, Marc L.
Functionalized oxepines via fragmentation of highly strained epoxides.
Organic letters, 2006, 8, 5183-5186
1506179 CIFC31 H31 I N P PdP -19.458; 11.332; 13.604
76.51; 86.68; 82.32
1404.6Beccalli, Egle M.; Broggini, Gianluigi; Martinelli, Michela; Masciocchi, Norberto; Sottocornola, Silvia
New 4-spiroannulated tetrahydroisoquinolines by a one-pot sequential procedure. isolation and characterization of sigma-alkylpalladium heck intermediates.
Organic letters, 2006, 8, 4521-4524
1506180 CIFC18 H16 O4P 1 21/c 17.2601; 17.0441; 11.6153
90; 105.116; 90
1387.6Sessions, E. Hampton; Jacobi, Peter A.
Studies on the synthesis of furanosteroids. I. Viridin models.
Organic letters, 2006, 8, 4125-4128
1506181 CIFC93.95 H22.6 N2 O4 S2.7C 1 2/c 153.619; 12.3613; 18.615
90; 108.317; 90
11713Chuang, Shih-Ching; Clemente, Fernando R.; Khan, Saeed I.; Houk, K. N.; Rubin, Yves
Approaches to open fullerenes: a 1,2,3,4,5,6-hexaadduct of C60.
Organic letters, 2006, 8, 4525-4528
1506182 CIFC11 H15 N5 O5P 21 21 216.1879; 6.6386; 30.879
90; 90; 90
1268.5Nowak, Ireneusz; Cannon, John F.; Robins, Morris J.
N-oxides of adenosine-type nucleosides undergo pyrimidine ring opening and closure to give 5-amino-4-(1,2,4-oxadiazol-3-yl)imidazole derivatives.
Organic letters, 2006, 8, 4565-4568
1506183 CIFC35 H33 N5 O8P 1 21 110.9634; 6.2492; 24.277
90; 97.714; 90
1648.23Nowak, Ireneusz; Cannon, John F.; Robins, Morris J.
N-oxides of adenosine-type nucleosides undergo pyrimidine ring opening and closure to give 5-amino-4-(1,2,4-oxadiazol-3-yl)imidazole derivatives.
Organic letters, 2006, 8, 4565-4568
1506184 CIFC8 H9 N5 O2P 1 21/n 16.9156; 9.5678; 14.8356
90; 97.897; 90
972.32Nowak, Ireneusz; Cannon, John F.; Robins, Morris J.
N-oxides of adenosine-type nucleosides undergo pyrimidine ring opening and closure to give 5-amino-4-(1,2,4-oxadiazol-3-yl)imidazole derivatives.
Organic letters, 2006, 8, 4565-4568
1506185 CIFC24 H27 N O6P 21 21 216.986; 11.755; 25.4
90; 90; 90
2086Feldman, Ken S.; Karatjas, Andrew G.
Extending Pummerer reaction chemistry. Asymmetric synthesis of spirocyclic oxindoles via chiral indole-2-sulfoxides.
Organic letters, 2006, 8, 4137-4140
1506186 CIFC26 H29 N O5P 32 2 112.794; 12.794; 24.424
90; 90; 120
3462.3Feldman, Ken S.; Karatjas, Andrew G.
Extending Pummerer reaction chemistry. Asymmetric synthesis of spirocyclic oxindoles via chiral indole-2-sulfoxides.
Organic letters, 2006, 8, 4137-4140
1506187 CIFC32 H40 O6P b c n26.12; 9.092; 11.853
90; 90; 90
2814.9Bérubé, Amélie; Drutu, Ioana; Wood, John L.
Progress toward the total synthesis of bacchopetiolone: application of a tandem aromatic oxidation/Diels-Alder reaction.
Organic letters, 2006, 8, 5421-5424
1506188 CIFC34 H24 N4 O4C 1 2/c 133.2904; 4.6499; 21.8825
90; 129.954; 90
2596.6Maes, Wouter; Van Rossom, Wim; Van Hecke, Kristof; Van Meervelt, Luc; Dehaen, Wim
Selective synthesis of functionalized thia- and oxacalix[2]arene[2]pyrimidines.
Organic letters, 2006, 8, 4161-4164
1506189 CIFC69 H51 Cl9 N4P 1 21/n 114.298; 9.036; 24.098
90; 103.915; 90
3022Higuchi, Masayoshi; Shomura, Ryo; Ohtsuka, Yuhki; Hayashi, Akari; Yamamoto, Kimihisa; Kurth, Dirk G.
Sequential metal ion assembly in cyclic phenylazomethine.
Organic letters, 2006, 8, 4723-4726
1506190 CIFC94 H70 Cl8P -110.4953; 12.5604; 18.7166
93.594; 102.2; 106.121
2297.33Wong, Ken-Tsung; Chi, Liang-Chen; Huang, Shih-Chiang; Liao, Yuan-Li; Liu, Yi-Hung; Wang, Yu
Coplanarity in the backbones of ladder-type oligo(p-phenylene) homologues and derivatives.
Organic letters, 2006, 8, 5029-5032
1506191 CIFC57 H43 Cl2C 1 2/c 128.4006; 10.1973; 16.7659
90; 113.988; 90
4436.19Wong, Ken-Tsung; Chi, Liang-Chen; Huang, Shih-Chiang; Liao, Yuan-Li; Liu, Yi-Hung; Wang, Yu
Coplanarity in the backbones of ladder-type oligo(p-phenylene) homologues and derivatives.
Organic letters, 2006, 8, 5029-5032
1506192 CIFC55 H46P -110.5923; 10.641; 10.6696
102.995; 109.818; 106.515
1013.57Wong, Ken-Tsung; Chi, Liang-Chen; Huang, Shih-Chiang; Liao, Yuan-Li; Liu, Yi-Hung; Wang, Yu
Coplanarity in the backbones of ladder-type oligo(p-phenylene) homologues and derivatives.
Organic letters, 2006, 8, 5029-5032
1506193 CIFC71 H56 Cl6P 1 21/n 19.9995; 21.0286; 28.2579
90; 97.321; 90
5893.5Wong, Ken-Tsung; Chi, Liang-Chen; Huang, Shih-Chiang; Liao, Yuan-Li; Liu, Yi-Hung; Wang, Yu
Coplanarity in the backbones of ladder-type oligo(p-phenylene) homologues and derivatives.
Organic letters, 2006, 8, 5029-5032
1506194 CIFC14 H28 B10 Si2P 1 21/c 115.8018; 10.593; 13.4179
90; 99.317; 90
2216.37Núñez, Rosario; Gonzalez-Campo, Arantzazu; Laromaine, Anna; Teixidor, Francesc; Sillanpää, Reijo; Kivekäs, Raikko; Viñas, Clara
Synthesis of small carboranylsilane dendrons as scaffolds for multiple functionalizations.
Organic letters, 2006, 8, 4549-4552
1506195 CIFC9 H22 B10 SiP -17.7775; 14.1714; 15.9281
96.034; 103.042; 100.443
1662.3Núñez, Rosario; Gonzalez-Campo, Arantzazu; Laromaine, Anna; Teixidor, Francesc; Sillanpää, Reijo; Kivekäs, Raikko; Viñas, Clara
Synthesis of small carboranylsilane dendrons as scaffolds for multiple functionalizations.
Organic letters, 2006, 8, 4549-4552
1506196 CIFC14 H24 B10 SiP 1 21/c 116.7308; 13.0118; 19.7733
90; 113.094; 90
3959.6Núñez, Rosario; Gonzalez-Campo, Arantzazu; Laromaine, Anna; Teixidor, Francesc; Sillanpää, Reijo; Kivekäs, Raikko; Viñas, Clara
Synthesis of small carboranylsilane dendrons as scaffolds for multiple functionalizations.
Organic letters, 2006, 8, 4549-4552
1506197 CIFC50 H44 O SP 1 21/n 115.884; 10.915; 23.3469
90; 109.874; 90
3806.7Wong, Ken-Tsung; Chao, Teng-Chih; Chi, Liang-Chen; Chu, Ying-Ying; Balaiah, Akula; Chiu, Shih-Feng; Liu, Yi-Hung; Wang, Yu
Syntheses and structures of novel heteroarene-fused coplanar pi-conjugated chromophores.
Organic letters, 2006, 8, 5033-5036
1506198 CIFC60 H45 NP -110.5328; 14.2613; 17.205
67.351; 72.196; 70.479
2200.91Wong, Ken-Tsung; Chao, Teng-Chih; Chi, Liang-Chen; Chu, Ying-Ying; Balaiah, Akula; Chiu, Shih-Feng; Liu, Yi-Hung; Wang, Yu
Syntheses and structures of novel heteroarene-fused coplanar pi-conjugated chromophores.
Organic letters, 2006, 8, 5033-5036
1506199 CIFC44 H34 S2P -19.0731; 14.1751; 14.4817
73.659; 81.407; 77.206
1735.34Wong, Ken-Tsung; Chao, Teng-Chih; Chi, Liang-Chen; Chu, Ying-Ying; Balaiah, Akula; Chiu, Shih-Feng; Liu, Yi-Hung; Wang, Yu
Syntheses and structures of novel heteroarene-fused coplanar pi-conjugated chromophores.
Organic letters, 2006, 8, 5033-5036
1506200 CIFC52 H38 S2P -19.8963; 10.7278; 10.7354
110.407; 104.026; 107.311
940.43Wong, Ken-Tsung; Chao, Teng-Chih; Chi, Liang-Chen; Chu, Ying-Ying; Balaiah, Akula; Chiu, Shih-Feng; Liu, Yi-Hung; Wang, Yu
Syntheses and structures of novel heteroarene-fused coplanar pi-conjugated chromophores.
Organic letters, 2006, 8, 5033-5036
1506201 CIFC46 H38 Cl4 S2P -110.3765; 10.4444; 10.7639
107.404; 109.796; 99.034
1003.08Wong, Ken-Tsung; Chao, Teng-Chih; Chi, Liang-Chen; Chu, Ying-Ying; Balaiah, Akula; Chiu, Shih-Feng; Liu, Yi-Hung; Wang, Yu
Syntheses and structures of novel heteroarene-fused coplanar pi-conjugated chromophores.
Organic letters, 2006, 8, 5033-5036
1506202 CIFC9.5 H11.5 N0.5 O S0.5P -15.03; 12.3658; 14.072
102.516; 95.968; 95.375
843.74Kim, Soo Min; Lee, Sang Ick; Chung, Young Keun
GaCl3-catalyzed formation of eight-membered rings from enynes bearing a cyclic olefin.
Organic letters, 2006, 8, 5425-5427
1506203 CIFC13 H14 Br N OP 21 21 215.5389; 8.4692; 27.111
90; 90; 90
1271.8Wender, Paul A.; Horan, Joshua C.
Synthesis and PKC binding of a new class of a-ring diversifiable bryostatin analogues utilizing a double asymmetric hydrogenation and cross-coupling strategy.
Organic letters, 2006, 8, 4581-4584
1506204 CIFC38 H54 Cl7 N O2 SiP 1 21/n 113.328; 22.154; 15.638
90; 108.17; 90
4387Kondo, Shin-Ichi; Harada, Tomomi; Tanaka, Ryoji; Unno, Masafumi
Anion recognition by a silanediol-based receptor.
Organic letters, 2006, 8, 4621-4624
1506205 CIFC28 H23 Br O5P 21 21 216.0107; 15.0074; 25.3448
90; 90; 90
2286.23Yeager, Adam R.; Min, Geanna K.; Porco, Jr, John A; Schaus, Scott E.
Exploring skeletal diversity via ring contraction of glycal-derived scaffolds.
Organic letters, 2006, 8, 5065-5068
1506206 CIFC26 H23 Br O5P 1 21 113.1894; 5.199; 17.152
90; 110.015; 90
1105.1Yeager, Adam R.; Min, Geanna K.; Porco, Jr, John A; Schaus, Scott E.
Exploring skeletal diversity via ring contraction of glycal-derived scaffolds.
Organic letters, 2006, 8, 5065-5068
1506207 CIFC23 H23 Br O5P 1 21 110.0462; 5.387; 19.6191
90; 100.504; 90
1043.97Yeager, Adam R.; Min, Geanna K.; Porco, Jr, John A; Schaus, Scott E.
Exploring skeletal diversity via ring contraction of glycal-derived scaffolds.
Organic letters, 2006, 8, 5065-5068
1506208 CIFC17 H18 N4P 1 21/c 17.4562; 16.273; 11.316
90; 95.83; 90
1365.9Gryko, Daniel T.; Piechowska, Joanna; Tasior, Mariusz; Waluk, Jacek; Orzanowska, Grazyna
From bifunctional nucleophilic behavior of DBU to a new heterocyclic fluorescent platform.
Organic letters, 2006, 8, 4747-4750
1506209 CIFC25 H31 N O3P 21 21 2110.447; 11.215; 37.269
90; 90; 90
4366.6Lebeuf, Raphaël; Robert, Frédéric; Schenk, Kurt; Landais, Yannick
Desymmetrization of cyclohexa-2,5-dienes through a diastereoselective protonation-hydroamination cascade.
Organic letters, 2006, 8, 4755-4758
1506210 CIFC14 H17 Cl O3 SP 1 21 16.8719; 8.3968; 12.8819
90; 98.659; 90
734.84Zhao, Hongda; Gorman, Jeffrey S. T.; Pagenkopf, Brian L.
Advances in Lewis acid controlled carbon-carbon bond-forming reactions enable a concise and convergent total synthesis of bullatacin.
Organic letters, 2006, 8, 4379-4382
1506211 CIFC25 H15 F12 N O SC 1 2/c 134.902; 9.072; 33.401
90; 109.749; 90
9954Kano, Naokazu; Daicho, Yuya; Kawashima, Takayuki
A potential intermediate for the aza-Corey-Chaykovsky reaction: synthesis, structure, and thermolysis of a pentacoordinate 1,2-thiazetidine 1-oxide.
Organic letters, 2006, 8, 4625-4627
1506212 CIFC25 H15 F12 N O2 SP n a 2110.371; 16.811; 14.108
90; 90; 90
2459.7Kano, Naokazu; Daicho, Yuya; Kawashima, Takayuki
A potential intermediate for the aza-Corey-Chaykovsky reaction: synthesis, structure, and thermolysis of a pentacoordinate 1,2-thiazetidine 1-oxide.
Organic letters, 2006, 8, 4625-4627
1506213 CIFC20 H27 N O6P 1 21/c 117.5139; 5.3838; 23.798
90; 121.842; 90
1906.2Coquerel, Yoann; Bensa, David; Doutheau, Alain; Rodriguez, Jean
Synthetic studies on the MARDi cascade: stereoselective synthesis of heterocyclic seven-membered rings.
Organic letters, 2006, 8, 4819-4822
1506214 CIFC11 H18 O6P 1 21/c 112.417; 5.357; 18.569
90; 96.63; 90
1226.91Coquerel, Yoann; Bensa, David; Doutheau, Alain; Rodriguez, Jean
Synthetic studies on the MARDi cascade: stereoselective synthesis of heterocyclic seven-membered rings.
Organic letters, 2006, 8, 4819-4822
1506215 CIFC64 H58 N2 S4P 1 21/n 123.094; 21.226; 27.759
90; 93.35; 90
13584Kumar, Rajeev; Misra, Rajneesh; Chandrashekar, Tavarekere K.
Effect of meso aryl substituents on the synthesis of core-modified expanded porphyrins.
Organic letters, 2006, 8, 4847-4850
1506216 CIFC117 H105 Fe6 O3P -120.19; 21.348; 24.339
98.401; 100.779; 115.219
9017Chebny, Vincent J.; Dhar, Dwairath; Lindeman, Sergey V.; Rathore, Rajendra
Simultaneous ejection of six electrons at a constant potential by hexakis(4-ferrocenylphenyl)benzene.
Organic letters, 2006, 8, 5041-5044
1506217 CIFC16 H13 Fe IC 1 c 17.8618; 23.0451; 15.497
90; 103.565; 90
2729.36Chebny, Vincent J.; Dhar, Dwairath; Lindeman, Sergey V.; Rathore, Rajendra
Simultaneous ejection of six electrons at a constant potential by hexakis(4-ferrocenylphenyl)benzene.
Organic letters, 2006, 8, 5041-5044
1506218 CIFC34 H26 Fe2P 1 21/c 112.6557; 7.8068; 12.6535
90; 104.579; 90
1209.92Chebny, Vincent J.; Dhar, Dwairath; Lindeman, Sergey V.; Rathore, Rajendra
Simultaneous ejection of six electrons at a constant potential by hexakis(4-ferrocenylphenyl)benzene.
Organic letters, 2006, 8, 5041-5044
1506219 CIFC22 H19 Br2 N OP 1 21/c 112.3611; 13.3819; 12.5042
90; 108.934; 90
1956.47Lazareva, Anna; Daugulis, Olafs
Direct palladium-catalyzed ortho-arylation of benzylamines.
Organic letters, 2006, 8, 5211-5213
1506220 CIFC21 H12 O2P 1 21/a 17.3419; 24.75; 7.8224
90; 107; 90
1359.3Moorthy, Jarugu Narasimha; Venkatakrishnan, Parthasarathy; Sengupta, Sanchita; Baidya, Mahiuddin
Facile synthesis, fluorescence, and photochromism of novel helical pyrones and chromenes.
Organic letters, 2006, 8, 4891-4894
1506221 CIFC21 H12 O2P 1 21/c 112.559; 5.626; 19.945
90; 104.03; 90
1367.2Moorthy, Jarugu Narasimha; Venkatakrishnan, Parthasarathy; Sengupta, Sanchita; Baidya, Mahiuddin
Facile synthesis, fluorescence, and photochromism of novel helical pyrones and chromenes.
Organic letters, 2006, 8, 4891-4894
1506222 CIFC22 H14 O2P 1 21/c 111.202; 7.167; 18.199
90; 94.155; 90
1457.3Moorthy, Jarugu Narasimha; Venkatakrishnan, Parthasarathy; Sengupta, Sanchita; Baidya, Mahiuddin
Facile synthesis, fluorescence, and photochromism of novel helical pyrones and chromenes.
Organic letters, 2006, 8, 4891-4894
1506223 CIFC22 H14 O2P 1 21/c 17.885; 26.061; 7.474
90; 111.659; 90
1427.4Moorthy, Jarugu Narasimha; Venkatakrishnan, Parthasarathy; Sengupta, Sanchita; Baidya, Mahiuddin
Facile synthesis, fluorescence, and photochromism of novel helical pyrones and chromenes.
Organic letters, 2006, 8, 4891-4894
1506224 CIFC24.5 H25 Cl Cu F12 N8 P2P n m a17.351; 23.605; 14.941
90; 90; 90
6119Gong, Han-Yuan; Zheng, Qi-Yu; Zhang, Xiao-Hang; Wang, De-Xian; Wang, Mei-Xiang
Methylazacalix[4]pyridine: en route to Zn2±specific fluoresence sensors.
Organic letters, 2006, 8, 4895-4898
1506225 CIFC21 H28 N4 O9P 1 21/c 18.4301; 25.655; 10.6102
90; 105.677; 90
2209.4Gerasyuto, Aleksey I.; Hsung, Richard P.
Stereodivergent total syntheses of precoccinelline, hippodamine, coccinelline, and convergine.
Organic letters, 2006, 8, 4899-4902
1506226 CIFC24 H32 O4P 1 21 16.0231; 18.81; 19.088
90; 91.44; 90
2161.9Kwiatkowski, Piotr; Majer, Jakub; Chaładaj, Wojciech; Jurczak, Janusz
Highly diastereoselective Friedel-Crafts reaction of furans with 8-phenylmenthyl glyoxylate.
Organic letters, 2006, 8, 5045-5048
1506227 CIFC20 N2 O2 SP 1 21/a 19.736; 15.884; 11.886
90; 97.432; 90
1822.7Falck, J. R.; He, Anyu; Reddy, L. Manmohan; Kundu, Abhijit; Barma, Deb K.; Bandyopadhyay, A.; Kamila, Sukanta; Akella, Radha; Bejot, Romain; Mioskowski, Charles
Ring expansion/homologation‒aldehyde condensation cascade using tert-trihalomethylcarbinols.
Organic letters, 2006, 8, 4645-4647
1506228 CIFC21 H24 N2 O2 SP -19.634; 9.858; 11.925
97.676; 97.61; 116.21
983.4Falck, J. R.; He, Anyu; Reddy, L. Manmohan; Kundu, Abhijit; Barma, Deb K.; Bandyopadhyay, A.; Kamila, Sukanta; Akella, Radha; Bejot, Romain; Mioskowski, Charles
Ring expansion/homologation–aldehyde condensation cascade using tert-trihalomethylcarbinols.
Organic letters, 2006, 8, 4645-4647
1506229 CIFC13 H15 Cl3 OP 21 21 215.982; 11.036; 20.476
90; 90; 90
1351.8Falck, J. R.; He, Anyu; Reddy, L. Manmohan; Kundu, Abhijit; Barma, Deb K.; Bandyopadhyay, A.; Kamila, Sukanta; Akella, Radha; Bejot, Romain; Mioskowski, Charles
Ring expansion/homologation–aldehyde condensation cascade using tert-trihalomethylcarbinols.
Organic letters, 2006, 8, 4645-4647
1506230 CIFC13 H15 Cl3 OP -111.499; 11.633; 21.44
82.286; 81.579; 76.573
2744.5Falck, J. R.; He, Anyu; Reddy, L. Manmohan; Kundu, Abhijit; Barma, Deb K.; Bandyopadhyay, A.; Kamila, Sukanta; Akella, Radha; Bejot, Romain; Mioskowski, Charles
Ring expansion/homologation–aldehyde condensation cascade using tert-trihalomethylcarbinols.
Organic letters, 2006, 8, 4645-4647
1506231 CIFC20 H20 OP 1 21 16.951; 7.903; 14.659
90; 101.766; 90
788.4Falck, J. R.; He, Anyu; Reddy, L. Manmohan; Kundu, Abhijit; Barma, Deb K.; Bandyopadhyay, A.; Kamila, Sukanta; Akella, Radha; Bejot, Romain; Mioskowski, Charles
Ring expansion/homologation–aldehyde condensation cascade using tert-trihalomethylcarbinols.
Organic letters, 2006, 8, 4645-4647
1506232 CIFC13 H15 Cl3 OP 1 21/c 17.544; 15.504; 11.984
90; 105.776; 90
1348.9Falck, J. R.; He, Anyu; Reddy, L. Manmohan; Kundu, Abhijit; Barma, Deb K.; Bandyopadhyay, A.; Kamila, Sukanta; Akella, Radha; Bejot, Romain; Mioskowski, Charles
Ring expansion/homologation–aldehyde condensation cascade using tert-trihalomethylcarbinols.
Organic letters, 2006, 8, 4645-4647
1506233 CIFC20 H20 OP 1 21/a 16.193; 17.433; 14.493
90; 99.693; 90
1542.4Falck, J. R.; He, Anyu; Reddy, L. Manmohan; Kundu, Abhijit; Barma, Deb K.; Bandyopadhyay, A.; Kamila, Sukanta; Akella, Radha; Bejot, Romain; Mioskowski, Charles
Ring expansion/homologation–aldehyde condensation cascade using tert-trihalomethylcarbinols.
Organic letters, 2006, 8, 4645-4647
1506234 CIFC13 H16 O2P c a 2111.2356; 5.4389; 19.1892
90; 90; 90
1172.64Jervis, Peter J.; Kariuki, Benson M.; Cox, Liam R.
Stereoselective synthesis of 2,4,5-trisubstituted tetrahydropyrans using an intramolecular allylation strategy.
Organic letters, 2006, 8, 4649-4652
1506235 CIFC25 H31 N O2P -110.1; 17.0482; 20.4921
102.669; 96.006; 106.526
3247.31Fleming, Fraser F.; Wei, Guoqing; Zhang, Zhiyu; Steward, Omar W.
Oxonitriles: a grignard addition-acylation route to enamides.
Organic letters, 2006, 8, 4903-4906
1506236 CIFC20 H29 N O2P 1 21/c 112.7515; 15.6796; 19.48
90; 104.275; 90
3774.54Fleming, Fraser F.; Wei, Guoqing; Zhang, Zhiyu; Steward, Omar W.
Oxonitriles: a grignard addition-acylation route to enamides.
Organic letters, 2006, 8, 4903-4906
1506237 CIFC12 H19 N O4 SiP 1 21/c 117.935; 6.408; 12.934
90; 99.607; 90
1465.6Hoye, Thomas R.; Dvornikovs, Vadims; Sizova, Elena
Silylative Dieckmann-like cyclizations of ester-imides (and diesters).
Organic letters, 2006, 8, 5191-5194
1506238 CIFC15 H27 N O6 SiP 21 21 217.7751; 15.225; 32.622
90; 90; 90
3861.7Hoye, Thomas R.; Dvornikovs, Vadims; Sizova, Elena
Silylative Dieckmann-like cyclizations of ester-imides (and diesters).
Organic letters, 2006, 8, 5191-5194
1506239 CIFC14 H13 Br O4P -17.928; 7.9969; 12.261
83.526; 78.836; 62.414
675.69Xu, Lubin; Huang, Xian; Zhong, Fangrui
Intermolecular tandem addition-cyclization of bromoallenes: a facile synthesis of methylenecyclopropyl carboxylates and polysubstituted furans.
Organic letters, 2006, 8, 5061-5064
1506240 CIFC40 H32 N2C 1 2/c 136.957; 9.8273; 16.7524
90; 104.949; 90
5878.3Kim, Hyunwoo; Yen, Cindy; Preston, Philippa; Chin, Jik
Substrate-directed stereoselectivity in vicinal diamine-catalyzed synthesis of warfarin.
Organic letters, 2006, 8, 5239-5242
1506241 CIFC25 H28 Cl2 N2 O8 SP 1 21 112.29; 9.62; 12.49
90; 100.76; 90
1451Li, Pixu; Forbeck, Erin M.; Evans, Cory D.; Joullié, Madeleine M
Trisubstituted aziridine ring-opening by phenol derivatives: stereo- and regioselective formation of chiral tertiary alkyl-aryl ethers.
Organic letters, 2006, 8, 5105-5107
1506242 CIFC42 H56 Cl2 N4 O12R 3 :H27.991; 27.991; 20.057
90; 90; 120
13609Hong, Wen-Xu; Chen, Ling-Jun; Zhong, Chun-Long; Yao, Zhu-Jun
Bidirectional synthesis of the central amino acid of chloptosin.
Organic letters, 2006, 8, 4919-4922
1506243 CIFC17 H19 N O2P n a 2120.5365; 5.2508; 26.4263
90; 90; 90
2849.63Banwell, Martin G.; Ma, Xinghua; Taylor, Rebecca M.; Willis, Anthony C.
Concise assembly of the polycyclic frameworks associated with the hapalindole and fischerindole alkaloids.
Organic letters, 2006, 8, 4959-4961
1506244 CIFC18 H23 NP -17.7435; 10.657; 18.3316
95.443; 97.0565; 103.869
1445.36Banwell, Martin G.; Ma, Xinghua; Taylor, Rebecca M.; Willis, Anthony C.
Concise assembly of the polycyclic frameworks associated with the hapalindole and fischerindole alkaloids.
Organic letters, 2006, 8, 4959-4961
1506245 CIFC18 H23 NP -17.9681; 10.7207; 18.021
96.5216; 98.1632; 104.245
1459.16Banwell, Martin G.; Ma, Xinghua; Taylor, Rebecca M.; Willis, Anthony C.
Concise assembly of the polycyclic frameworks associated with the hapalindole and fischerindole alkaloids.
Organic letters, 2006, 8, 4959-4961
1506246 CIFC22 H15 N3 O5P 1 21/c 113.7213; 7.7011; 19.5546
90; 110.252; 90
1938.6Pinto, Artur; Neuville, Luc; Retailleau, Pascal; Zhu, Jieping
Synthesis of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process.
Organic letters, 2006, 8, 4927-4930
1506247 CIFC23 H18 N2 O4P 1 21/c 19.712; 27.09; 7.598
90; 103.46; 90
1944.1Pinto, Artur; Neuville, Luc; Retailleau, Pascal; Zhu, Jieping
Synthesis of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process.
Organic letters, 2006, 8, 4927-4930
1506248 CIFC16 H12 N2 O2P 1 21/c 14.4469; 11.4613; 26.073
90; 93.528; 90
1326.35Dai, Weixiang; Petersen, Jeffrey L.; Wang, Kung K.
Synthesis of the parent and substituted tetracyclic ABCD ring cores of camptothecins via 1-(3-aryl-2-propynyl)- 1,6-dihydro-6-oxo-2-pyridinecarbonitriles.
Organic letters, 2006, 8, 4665-4667
1506249 CIFC15 H10 N2 OP 1 21/n 113.961; 4.8222; 17.468
90; 108.14; 90
1117.5Dai, Weixiang; Petersen, Jeffrey L.; Wang, Kung K.
Synthesis of the parent and substituted tetracyclic ABCD ring cores of camptothecins via 1-(3-aryl-2-propynyl)- 1,6-dihydro-6-oxo-2-pyridinecarbonitriles.
Organic letters, 2006, 8, 4665-4667
1506250 CIFC16 H12 N2 O2P 1 21/n 17.164; 20.24; 9.0634
90; 110.805; 90
1228.5Dai, Weixiang; Petersen, Jeffrey L.; Wang, Kung K.
Synthesis of the parent and substituted tetracyclic ABCD ring cores of camptothecins via 1-(3-aryl-2-propynyl)- 1,6-dihydro-6-oxo-2-pyridinecarbonitriles.
Organic letters, 2006, 8, 4665-4667
1506251 CIFC39 H46 Cl4 N4 PdP -110.2921; 11.3599; 17.186
74.811; 77.22; 76.606
1858.6Xu, Linlin; Ferrence, Gregory M.; Lash, Timothy D.
[22]Porphyrin-(3.1.1.3), a new vinylogous expanded porphyrin system.
Organic letters, 2006, 8, 5113-5116
1506252 CIFC22 H17 N O4 SP 1 21/c 113.9922; 15.3095; 8.5436
90; 98.035; 90
1812.2Lauchli, Ryan; Shea, Kenneth J.
A synthesis of the welwistatin core.
Organic letters, 2006, 8, 5287-5289

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 5268 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!