Crystallography Open Database

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Searching year of publication is 2009

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1504122 CIFC23 H21 Br N O4 SP -110.503; 11.062; 12.012
91.99; 112.83; 116.73
1111.1Wei, Jun-Fa; Chen, Zhan-Guo; Lei, Wei; Zhang, Li-Hui; Wang, Ming-Zheng; Shi, Xian-Ying; Li, Run-Tao
Silicon powder: the first nonmetal elemental catalyst for aminobromination of olefins with TsNH(2) and NBS.
Organic letters, 2009, 11, 4216-4219
1504123 CIFC21 H12 N2 OP n a 2115.884; 4.626; 19.4181
90; 90; 90
1426.83Haag, Benjamin; Peng, Zhihua; Knochel, Paul
Preparation of polyfunctional indazoles and heteroarylazo compounds using highly functionalized zinc reagents.
Organic letters, 2009, 11, 4270-4273
1504124 CIFC18 H20 O6P 1 21/c 19.117; 8.628; 19.717
90; 95.16; 90
1544.7Geng, Chang-An; Jiang, Zhi-Yong; Ma, Yun-Bao; Luo, Jie; Zhang, Xue-Mei; Wang, Hong-Ling; Shen, Yong; Zuo, Ai-Xue; Zhou, Jun; Chen, Ji-Jun
Swerilactones A and B, anti-HBV new lactones from a tradtional Chinese herb: Swertia mileensis as a treatment for viral hepatitis.
Organic letters, 2009, 11, 4120-4123
1504125 CIFC18 H21 O6P 1 c 17.4578; 15.834; 7.0431
90; 111.745; 90
772.5Geng, Chang-An; Jiang, Zhi-Yong; Ma, Yun-Bao; Luo, Jie; Zhang, Xue-Mei; Wang, Hong-Ling; Shen, Yong; Zuo, Ai-Xue; Zhou, Jun; Chen, Ji-Jun
Swerilactones A and B, anti-HBV new lactones from a tradtional Chinese herb: Swertia mileensis as a treatment for viral hepatitis.
Organic letters, 2009, 11, 4120-4123
1504126 CIFC24 H12C 1 2/c 119.932; 11.06; 15.993
90; 125.953; 90
2854Umeda, Rui; Hibi, Daijiro; Miki, Koji; Tobe, Yoshito
Tetradehydrodinaphtho[10]annulene: a hitherto unknown dehydroannulene and a viable precursor to stable zethrene derivatives.
Organic letters, 2009, 11, 4104-4106
1504127 CIFC15 H15 Cl O2P 21 21 215.2032; 12.4052; 20.7454
90; 90; 90
1339.05Marqués-López, Eugenia; Herrera, Raquel P.; Marks, Timo; Jacobs, Wiebke C.; Könning, Daniel; de Figueiredo, Renata M.; Christmann, Mathias
Crossed intramolecular Rauhut-Currier-type reactions via dienamine activation.
Organic letters, 2009, 11, 4116-4119
1504128 CIFC42 H52 N4 O3P 1 21 112.7151; 8.5294; 17.2463
90; 108.811; 90
1770.5Gan, Chew-Yan; Robinson, Ward T.; Etoh, Tadahiro; Hayashi, Masahiko; Komiyama, Kanki; Kam, Toh-Seok
Leucophyllidine, a cytotoxic bisindole alkaloid constituted from the union of an eburnan and a new vinylquinoline alkaloid.
Organic letters, 2009, 11, 3962-3965
1504129 CIFC20 H20 O7P -16.9331; 8.3871; 16.424
102.313; 91.417; 97.461
923.81Zheng, Suqing; Lu, Xiyan
Phosphine-catalyzed [4 + 3] annulation for the synthesis of highly functionalized bicyclo[3.2.2]nonadienes.
Organic letters, 2009, 11, 3978-3981
1504130 CIFC98 H104 Cl8 N4 O2P 1 21/c 114.7357; 17.0703; 17.6198
90; 105.354; 90
4273.94Stepień, Marcin; Szyszko, Bartosz; Latos-Grazyński, Lechosław
Steric control in the synthesis of p-benziporphyrins. Formation of a doubly N-confused benzihexaphyrin macrocycle.
Organic letters, 2009, 11, 3930-3933
1504131 CIFC12 H6 O6A b a 210.4174; 37.939; 10.277
90; 90; 90
4061.7Li, Yan; Lampkins, Andrew J.; Baker, Matthew B.; Sumpter, Bobby G.; Huang, Jingsong; Abboud, Khalil A.; Castellano, Ronald K.
Benzotrifuranone: synthesis, structure, and access to polycyclic heteroaromatics.
Organic letters, 2009, 11, 4314-4317
1504132 CIFC18 B2 F12 O4P 1 21/n 15.998; 14.15; 9.877
90; 92.99; 90
837Ono, Katsuhiko; Hashizume, Junko; Yamaguchi, Hiroyuki; Tomura, Masaaki; Nishida, Jun-ichi; Yamashita, Yoshiro
Synthesis, crystal structure, and electron-accepting property of the BF2 complex of a dihydroxydione with a perfluorotetracene skeleton.
Organic letters, 2009, 11, 4326-4329
1504133 CIFC12 H16 N2 O3 SP 1 21/n 16.2673; 25.0168; 8.7697
90; 105.982; 90
1321.84Pelletier, Sophie M.-C.; Ray, Peter C.; Dixon, Darren J.
Nitro-Mannich/lactamization cascades for the direct stereoselective synthesis of pyrrolidin-2-ones.
Organic letters, 2009, 11, 4512-4515
1504134 CIFC6 H7 Cl O3P 21 21 216.2776; 8.4084; 12.6034
90; 90; 90
665.27Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic access to versatile epoxyquinol synthons.
Organic letters, 2009, 11, 4290-4293
1504135 CIFC6 H7 Br O3P 21 21 216.4569; 8.5563; 12.5272
90; 90; 90
692.09Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic access to versatile epoxyquinol synthons.
Organic letters, 2009, 11, 4290-4293
1504136 CIFC6 H7 I O3P 21 21 216.8869; 8.8262; 12.2911
90; 90; 90
747.12Pinkerton, David M.; Banwell, Martin G.; Willis, Anthony C.
Chemoenzymatic access to versatile epoxyquinol synthons.
Organic letters, 2009, 11, 4290-4293
1504137 CIFC25 H19 N O4P 21 21 216.2109; 15.5608; 21.4507
90; 90; 90
2073.1Nibbs, Antoinette E.; Baize, Amanda-Lauren; Herter, Rachel M.; Scheidt, Karl A.
Catalytic asymmetric alkylation of substituted isoflavanones.
Organic letters, 2009, 11, 4010-4013
1504138 CIFC27 H27 Br N2 O6 S SiP 1 21/n 115.3551; 21.005; 17.9066
90; 92.464; 90
5770.1Brawn, Ryan A.; Panek, James S.
Synthesis of enantioenriched homopropargylic sulfonamides by a three component reaction of aldehydes, sulfonamides, and chiral allenylsilanes.
Organic letters, 2009, 11, 4362-4365
1504139 CIFC20 H14 Br2P 1 21/c 19.4002; 12.978; 6.5114
90; 98.955; 90
784.7Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504140 CIFC20 H14 I2P 1 21/c 18.8964; 4.3883; 20.521
90; 91.043; 90
801Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504141 CIFC20 H14 Cl2P 1 21/c 19.0002; 12.78; 6.5335
90; 98.782; 90
742.7Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504142 CIFC20 H14 F2P 1 21/c 18.272; 12.739; 6.63
90; 100.662; 90
686.6Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504143 CIFC20 H14 Br2P 1 21/n 14.8281; 20.915; 7.4401
90; 90.051; 90
751.3Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504144 CIFC20 H14P b c a7.9296; 11.5575; 14.399
90; 90; 90
1319.6Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504145 CIFC40 H40P -110.432; 11.282; 13.32
102.375; 92.892; 106.548
1457.4Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504146 CIFC20 H14 Br2P 1 21/n 128.496; 4.0216; 29.455
90; 110.436; 90
3163.1Isobe, Hiroyuki; Hitosugi, Shunpei; Matsuno, Taisuke; Iwamoto, Takeaki; Ichikawa, Junji
Concise synthesis of halogenated chrysenes ([4]phenacenes) that favor pi-stack packing in single crystals.
Organic letters, 2009, 11, 4026-4028
1504147 CIFC18 H19 N O5C 1 c 114.725; 16.2; 6.768
90; 91.991; 90
1613Barabé, Francis; Bétournay, Geneviève; Bellavance, Gabriel; Barriault, Louis
Gold-catalyzed synthesis of carbon-bridged medium-sized rings.
Organic letters, 2009, 11, 4236-4238
1504148 CIFC22 H18 Cl2 OP 1 21 110.5484; 8.7351; 10.6236
90; 114.794; 90
888.64Ji, Yining; Riera, Antoni; Verdaguer, Xavier
Asymmetric intermolecular Pauson-Khand reaction of symmetrically substituted alkynes.
Organic letters, 2009, 11, 4346-4349
1504149 CIFC14 H21 N5 O4 SeP -16.2068; 10.0735; 14.6424
105.53; 94.385; 97.243
869.2Goswami, Shyamaprosad; Hazra, Anita; Chakrabarty, Rinku; Fun, Hoong-Kun
Recognition of carboxylate anions and carboxylic acids by selenium-based new chromogenic fluorescent sensor: a remarkable fluorescence enhancement of hindered carboxylates.
Organic letters, 2009, 11, 4350-4353
1504150 CIFC16 H26 N2 O4R -3 :H28.99; 28.99; 10.1877
90; 90; 120
7414.9Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions.
Organic letters, 2009, 11, 4540-4543
1504151 CIFC21 H31 N2 O4P -18.834; 10.2781; 13.2981
90.009; 106.126; 98.122
1147.3Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions.
Organic letters, 2009, 11, 4540-4543
1504152 CIFC21 H38 N2 O7P -110.3811; 11.0624; 11.7553
109.649; 93.374; 115.456
1114.6Chen, Peiling; Carroll, Patrick J.; Sieburth, Scott McN
3-4'-Bipiperidines via sequential [4 + 4]-[3,3]-retro-Mannich reactions.
Organic letters, 2009, 11, 4540-4543
1504153 CIFC34 H25 Br N4P 1 21/c 19.5831; 13.0254; 23.2091
90; 96.634; 90
2877.6Yeagley, Andrew A.; Lowder, Melissa A.; Chruma, Jason J.
Tandem C-C bond-forming processes: interception of the pd-catalyzed decarboxylative allylation of allyl diphenylglycinate imines with activated olefins.
Organic letters, 2009, 11, 4022-4025
1504154 CIFC141 H88 F8P -114.2342; 16.3982; 23.0578
106.176; 91.373; 106.571
4922.9Thirion, Damien; Poriel, Cyril; Barrière, Frédéric; Métivier, Rémi; Jeannin, Olivier; Rault-Berthelot, Joëlle
Tuning the optical properties of aryl-substituted dispirofluorene-indenofluorene isomers through intramolecular excimer formation.
Organic letters, 2009, 11, 4794-4797
1504155 CIFC13 H8 N2 O2 S2P 1 21/n 17.4427; 9.3482; 18.2369
90; 95.639; 90
1262.71Murru, Siva; Ghosh, Harisadhan; Sahoo, Santosh K.; Patel, Bhisma K.
Intra- and intermolecular C-S bond formation using a single catalytic system: first direct access to arylthiobenzothiazoles.
Organic letters, 2009, 11, 4254-4257
1504156 CIFC28 H26 N2 O7 SP 1 21/c 111.33; 10.825; 21.832
90; 96.054; 90
2662.7Schuler, Marie; Duvvuru, Deepti; Retailleau, Pascal; Betzer, Jean-François; Marinetti, Angela
New access to trisubstituted 3-pyrrolines under phosphine catalysis.
Organic letters, 2009, 11, 4406-4409
1504157 CIFC33 H43 Br O5P 1 21/n 118.028; 8.953; 19.479
90; 98.94; 90
3105.8Couladouros, Elias A.; Dakanali, Marianna; Demadis, Konstantinos D.; Vidali, Veroniki P.
A short biomimetic approach to the fully functionalized bicyclic framework of type A acylphloroglucinols.
Organic letters, 2009, 11, 4430-4433
1504158 CIFC34 H56 N12 O17P 1 21/m 110.4708; 19.8848; 10.7309
90; 116.395; 90
2001.36Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504159 CIFC46 H59 I2 N14 O11.5P 1 21/c 115.4095; 13.0685; 25.1488
90; 94.613; 90
5048.04Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504160 CIFC46 H60 I2 N14 O13P 1 21/n 114.5007; 13.3573; 27.3613
90; 93.266; 90
5291Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504161 CIFC41 H58 I N13 O14P 1 21/n 113.0994; 14.8054; 24.1661
90; 92.029; 90
4683.88Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504162 CIFC24 H38 N12 O10P 1 21/c 19.4511; 13.8492; 21.2892
90; 99.131; 90
2751.24Stancl, Marek; Hodan, Martin; Sindelar, Vladimir
Glycoluril trimers: selective synthesis and supramolecular properties.
Organic letters, 2009, 11, 4184-4187
1504163 CIFC18 H15 Br O2P 21 21 215.7231; 12.9531; 20.0245
90; 90; 90
1484.45Gregg, Timothy M.; Farrugia, Mark K.; Frost, John R.
Rhodium-mediated enantioselective cyclopropanation of allenes.
Organic letters, 2009, 11, 4434-4436
1504164 CIFC45 H40 N4 O5.5P 1 21/c 113.2356; 12.1782; 26.593
90; 102.202; 90
4189.6Zhou, Ying; Wang, Fang; Kim, Youngmee; Kim, Sung-Jin; Yoon, Juyoung
Cu2±selective ratiometric and "off-on" sensor based on the rhodamine derivative bearing pyrene group.
Organic letters, 2009, 11, 4442-4445
1504165 CIFC24 N2 O2P 1 21/n 19.668; 9.511; 19.728
90; 90.66; 90
1813.9Zhou, Ying; Wang, Fang; Kim, Youngmee; Kim, Sung-Jin; Yoon, Juyoung
Cu2±selective ratiometric and "off-on" sensor based on the rhodamine derivative bearing pyrene group.
Organic letters, 2009, 11, 4442-4445
1504166 CIFC392 H360 F48 N8 O48 P8P 1 21/n 116; 24.7; 24.3
90; 103.4; 90
9342Cao, Jing; Lu, Hai-Yan; You, Xiao-Jun; Zheng, Qi-Yu; Chen, Chuan-Feng
Complexation of a pentiptycene-based tweezer-like receptor with paraquat derivatives: ion-controlled binding and release of the guests.
Organic letters, 2009, 11, 4446-4449
1504167 CIFC20 H14 N4 SP 1 21/c 18.9001; 11.3943; 14.9742
90; 91.902; 90
1517.7Balaji, Ganapathy; Shim, Wong Low; Parameswaran, Manoj; Valiyaveettil, Suresh
Thiadiazole fused indolo[2,3-a]carbazole based oligomers and polymer.
Organic letters, 2009, 11, 4450-4453
1504168 CIFC39 H40 O6 S4P -111.784; 15.222; 20.955
100.82; 102.15; 90.23
3605.6Kundrat, Ondrej; Dvorakova, Hana; Cisarova, Ivana; Pojarova, Michaela; Lhotak, Pavel
Unusual intramolecular bridging reaction in thiacalix[4]arene series.
Organic letters, 2009, 11, 4188-4191
1504169 CIFC25 H27 N3 O3P 1 21/c 19.7384; 12.008; 19.3474
90; 94.943; 90
2254Jiang, Gaoxi; Chen, Jian; Huang, Jie-Sheng; Che, Chi-Ming
Highly efficient oxidation of amines to imines by singlet oxygen and its application in Ugi-type reactions.
Organic letters, 2009, 11, 4568-4571
1504170 CIFC16 H22 O SP 1 21/n 113.777; 6.552; 16.81
90; 108.452; 90
1439.4Liu, Taoping; Zhao, Xiaoming; Lu, Long; Cohen, Theodore
Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent.
Organic letters, 2009, 11, 4576-4579
1504171 CIFC18 H24 O SP b c a9.2519; 16.7091; 20.816
90; 90; 90
3218Liu, Taoping; Zhao, Xiaoming; Lu, Long; Cohen, Theodore
Readily prepared 3-chloro-1-(phenylthio)propene, a versatile three-carbon annulating agent.
Organic letters, 2009, 11, 4576-4579
1504172 CIFC13 H20 N2 SiP n a 2110.6; 14.995; 8.7526
90; 90; 90
1391.2Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng
Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes.
Organic letters, 2009, 11, 4458-4461
1504173 CIFC27 H30 N4 O2 SiP -112.696; 14.502; 15.33
74.95; 71.74; 79.67
2573.6Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng
Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes.
Organic letters, 2009, 11, 4458-4461
1504174 CIFC31 H29 Br3 N6 O4P -110.299; 12.584; 12.776
82.36; 88.14; 72.95
1568.9Zhang, Hui-Jun; Meng, Tianhao; Demerseman, Bernard; Bruneau, Christian; Xi, Zhenfeng
Hydride-induced novel cyclization of dienedinitriles leading to multifunctionalized cyclopentadienes.
Organic letters, 2009, 11, 4458-4461
1504175 CIFC84 H27 Cl2 N O SiP 1 21/n 119.1274; 13.9545; 19.5256
90; 108.304; 90
4947.96Matsuo, Keiko; Matsuo, Yutaka; Iwashita, Akihiko; Nakamura, Eiichi
Synthesis of imino[60]fullerenes using nitriles and trimethylsilylmethyl triflate.
Organic letters, 2009, 11, 4192-4194
1504176 CIFC22 H26 N2 O2P 1 21/c 18.816; 13.762; 31.213
90; 94.584; 90
3774.83Grant, Christopher D.; Krische, Michael J.
Protecting-group-free synthesis of 3-tert-prenylated oxindoles: contiguous all-carbon quaternary centers via tertiary neopentyl substitution.
Organic letters, 2009, 11, 4485-4487
1504177 CIFC22 H19 N O5P 21 21 215.7776; 16.337; 20.021
90; 90; 90
1889.8Li, Hongyan; Hsung, Richard P.
Highly substituted 2-amido-furans from Rh(II)-catalyzed cyclopropenations of ynamides.
Organic letters, 2009, 11, 4462-4465
1504178 CIFC79 H95 F12 N7 O16 P2P -114.3156; 15.2385; 21.0682
86.801; 82.424; 66.377
4174.1Yen, Ming-Liang; Chen, Nai-Chia; Lai, Chien-Chen; Liu, Yi-Hung; Peng, Shie-Ming; Chiu, Sheng-Hsien
A molecular cage that selectively complexes three different guests in solution.
Organic letters, 2009, 11, 4604-4607
1504179 CIFC28 H27 Cl Cu0.5 N9 O2P -19.6706; 11.7736; 12.4516
80.677; 81.72; 81.309
1372.5Ozçubukçu, Salih; Ozkal, Erhan; Jimeno, Ciril; Pericàs, Miquel A
A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure.
Organic letters, 2009, 11, 4680-4683
1504180 CIFC20 H20 O8P 1 21 16.547; 10.892; 12.418
90; 103.542; 90
860.9Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun
Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis.
Organic letters, 2009, 11, 4838-4841
1504181 CIFC20 H22 O9P -18.6844; 14.094; 17
73.293; 87.688; 72.958
1903.2Geng, Chang-An; Zhang, Xue-Mei; Shen, Yong; Zuo, Ai-Xue; Liu, Ji-Feng; Ma, Yun-Bao; Luo, Jie; Zhou, Jun; Jiang, Zhi-yong; Chen, Ji-Jun
Swerilactones C and D, anti-HBV new lactones from a traditional Chinese herb: Swertia mileensis.
Organic letters, 2009, 11, 4838-4841
1504182 CIFC24 H36 Cl N2 O7P 21 21 219.268; 13.934; 19.073
90; 90; 90
2463.1Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong
Melohenines A and B, two unprecedented alkaloids from Melodinus henryi
Organic Letters, 2009, 11, 4834-4837
1504183 CIFC19 H24 N2 O3P 21 21 217.9717; 12.2181; 17.265
90; 90; 90
1681.6Feng, Tao; Cai, Xiang-Hai; Li, Yan; Wang, Yuan-Yuan; Liu, Ya-Ping; Xie, Ming-Jin; Luo, Xiao-Dong
Melohenines A and B, two unprecedented alkaloids from Melodinus henryi
Organic Letters, 2009, 11, 4834-4837
1504184 CIFC15 H11 N3 O2P 1 21/c 119.1116; 4.165; 16.2443
90; 111.391; 90
1203.97Board, Johnathan; Wang, Jian-Xin; Crew, Andrew P.; Jin, Meizhong; Foreman, Kenneth; Mulvihill, Mark J.; Snieckus, Victor
Synthesis of substituted imidazo[1,5-a]pyrazines via mono-, di-, and directed remote metalation strategies.
Organic letters, 2009, 11, 5118-5121
1504185 CIFC16 H18 O4C 1 2 118.1933; 7.711; 12.4502
90; 129.39; 90
1349.87Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504186 CIFC16 H18 O5P 21 21 217.8053; 9.4883; 18.9039
90; 90; 90
1400Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504187 CIFC17 H20 O5C 1 2 118.1525; 7.6684; 12.0226
90; 101.178; 90
1641.81Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504188 CIFC16 H18 O5P 21 21 219.597; 9.9935; 14.1873
90; 90; 90
1360.67Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504189 CIFC19 H24 O4P 21 21 217.7249; 9.6338; 22.5067
90; 90; 90
1674.95Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504190 CIFC19 H22 O4P 21 21 217.7635; 9.7864; 21.0195
90; 90; 90
1596.99Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504191 CIFC17 H20 O6P 21 21 216.1894; 8.9465; 28.8255
90; 90; 90
1596.17Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504192 CIFC16 H18 O6P 21 21 218.2864; 10.0771; 17.1744
90; 90; 90
1434.11Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504193 CIFC17 H20 O6P 21 21 2111.0321; 11.6526; 11.9913
90; 90; 90
1541.51Hanessian, Stephen; Boyer, Nicolas; Reddy, Gone Jayapal; Deschênes-Simard, Benoît
Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F.
Organic letters, 2009, 11, 4640-4643
1504194 CIFC15 H22 O3P -18.8984; 9.621; 16.7771
89.599; 85.959; 85.973
1429.2Hampel, Thomas; Brückner, Reinhard
A novel cis-selective cyclohexanone annulation as the key step of a total synthesis of the sesquiterpene isoacanthodoral.
Organic letters, 2009, 11, 4842-4845
1504195 CIFC18 H13 F3 O9 SP 1 21/c 118.964; 13.633; 29.823
90; 92.316; 90
7704Cui, Yi; Jiang, Hao; Li, Zhengtao; Wu, Na; Yang, Zhen; Quan, Junmin
Unexpected regioselectivity in the synthesis of pyranonaphthoquinone via the Diels-Alder reaction.
Organic letters, 2009, 11, 4628-4631
1504196 CIFC9 H12 O3 SP 1 21 17.6288; 5.445; 11.5547
90; 91.844; 90
479.72Majer, Jakub; Kwiatkowski, Piotr; Jurczak, Janusz
Highly enantioselective Friedel-Crafts reaction of thiophenes with glyoxylates: formal synthesis of duloxetine.
Organic letters, 2009, 11, 4636-4639
1504197 CIFC18 H27 N O6P 21 21 219.355; 11.918; 17.31
90; 90; 90
1929.9Gross, Ulrike; Nieger, Martin; Bräse, Stefan
Stereoselective synthesis of the epicoccin core.
Organic letters, 2009, 11, 4740-4742
1504198 CIFC22 H27 N O7P 1 21 17.715; 15.086; 9.295
90; 96.54; 90
1074.8Balthaser, Bradley R.; McDonald, Frank E.
Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins.
Organic letters, 2009, 11, 4850-4853
1504199 CIFC22 H27 N O7P 1 21 113.2879; 9.2997; 17.411
90; 100.194; 90
2117.57Balthaser, Bradley R.; McDonald, Frank E.
Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins.
Organic letters, 2009, 11, 4850-4853
1504200 CIFC22 H35 N O11P 21 21 218.1737; 10.9997; 29.222
90; 90; 90
2627.3Balthaser, Bradley R.; McDonald, Frank E.
Brønsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins.
Organic letters, 2009, 11, 4850-4853
1504201 CIFC28.5 H31 ClC 1 2/c 125.9973; 12.3802; 13.8796
90; 93.724; 90
4457.74Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504202 CIFC30 H34P -111.075; 14.841; 15.693
118.089; 91.405; 92.655
2270Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504203 CIFC30 H34 O2P 1 21/c 110.6975; 10.0435; 10.8065
90; 101.43; 90
1138.03Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504204 CIFC30 H34 O2P 1 21/c 114.0575; 10.3006; 8.0732
90; 99.533; 90
1152.86Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504205 CIFC30 H34 O2.96R -3 :H21.0561; 21.0561; 14.3941
90; 90; 120
5526.77Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504206 CIFC32 H38 O4P 1 21/n 19.6612; 6.9042; 19.3657
90; 94.574; 90
1287.63Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504207 CIFC48 H54P 1 21/c 121.8162; 9.4664; 8.9027
90; 90.648; 90
1838.5Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504208 CIFC66 H86P 1 21/n 111.9837; 36.2583; 18.6597
90; 95.013; 90
8076.8Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504209 CIFC40 H50 Cl4 O4P 1 21/c 112.5705; 9.6243; 15.996
90; 106.347; 90
1857Modjewski, Matthew; Lindeman, Sergey V.; Rathore, Rajendra
A versatile preparation of Geländer-type p-terphenyls from a readily available diacetylenic precursor.
Organic letters, 2009, 11, 4656-4659
1504210 CIFC23 H22 Cl N O3P 1 21 110.185; 8.74; 12.189
90; 112.29; 90
1003.9Han, Bo; Xiao, You-Cai; He, Zhao-Quan; Chen, Ying-Chun
Asymmetric Michael addition of gamma,gamma-disubstituted alpha,beta-unsaturated aldehydes to nitroolefins via dienamine catalysis.
Organic letters, 2009, 11, 4660-4663
1504211 CIFC12 H9 N O4P 1 21/n 16.0584; 19.717; 8.9513
90; 98.257; 90
1058.2Huo, Fang-Jun; Sun, Yuan-Qiang; Su, Jing; Chao, Jian-Bin; Zhi, Hai-Juan; Yin, Cai-Xia
Colorimetric detection of thiols using a chromene molecule
Organic letters, 2009, 11, 4918-4921
1504212 CIFC17 H15 B F4 O3P 1 21/n 112.7974; 7.6261; 17.351
90; 105.01; 90
1635.6Hu, Zhi-Long; Qian, Wen-Jian; Wang, Sheng; Wang, Shaozhong; Yao, Zhu-Jun
Transformation of reactive isochromenylium intermediates to stable salts and their cascade reactions with olefins.
Organic letters, 2009, 11, 4676-4679
1504213 CIFC21 H28 O10P 21 21 2110.0245; 12.5364; 17.6378
90; 90; 90
2216.6Afarinkia, Kamyar; Abdullahi, Mohamed Haji; Scowen, Ian J.
A new, general method for the synthesis of carbasugar-sugar pseudodisaccharides.
Organic letters, 2009, 11, 5182-5184
1504214 CIFC25 H40 O5 SiP 21 21 216.5381; 13.0869; 28.301
90; 90; 90
2421.5Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504215 CIFC27 H40 O7 SiC 1 2 127.8634; 7.012; 18.3625
90; 129.332; 90
2774.98Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504216 CIFC21 H24 O6P 1 21/n 17.1446; 10.9191; 23.7565
90; 91.941; 90
1852.24Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504217 CIFC21 H27 O7C 1 2 130.4299; 7.0493; 19.6268
90; 111.309; 90
3922.31Krawczuk, Paul J.; Schöne, Niklas; Baran, Phil S.
A synthesis of the carbon skeleton of maoecrystal V.
Organic letters, 2009, 11, 4774-4776
1504218 CIFC26 H21 O3P 18.4452; 10.6647; 11.566
82.23; 89.149; 77.425
1007.26Yoshida, Masahiro; Higuchi, Mariko; Shishido, Kozo
Stereoselective construction of substituted chromans by palladium-catalyzed cyclization of propargylic carbonates with 2-(2-hydroxyphenyl)acetates.
Organic letters, 2009, 11, 4752-4755
1504219 CIFC26 H33 N O3 SiP 17.718; 11.898; 14.296
96.932; 103.456; 108.338
1184.9Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar
Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process.
Organic letters, 2009, 11, 5230-5233
1504220 CIFC18 H21 N O4P 1 21/n 110.762; 12.294; 11.66
90; 106.56; 90
1478.7Tietze, Lutz F.; Tölle, Nina; Kratzert, Daniel; Stalke, Dietmar
Efficient formal total synthesis of the erythrina alkaloid (+)-erysotramidine, using a domino process.
Organic letters, 2009, 11, 5230-5233
1504221 CIFC29 H22 O2C 1 2/c 125.5017; 10.0101; 18.5411
90; 118.749; 90
4149.6Zhang, Xiaoxiang; Teo, Wan Teng; Chan, Philip Wai Hong
Ytterbium(III) triflate catalyzed tandem Friedel-Crafts alkylation/hydroarylation of propargylic alcohols with phenols as an expedient route to indenols.
Organic letters, 2009, 11, 4990-4993

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