Crystallography Open Database

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Searching year of publication is 2009

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1503922 CIFC10 H7 Cl N2P 1 21/c 19.958; 14.194; 6.82
90; 109.25; 90		910.1Li, Xiaoxun; Du, Yunfei; Liang, Zhidan; Li, Xiangke; Pan, Yan; Zhao, Kang
Simple conversion of enamines to 2H-azirines and their rearrangements under thermal conditions.
Organic letters, 2009, 11, 2643-2646
1503923 CIFC11 H10 N2 O3P -16.9189; 7.062; 11.947
74.48; 74.71; 66.39		507.2Li, Xiaoxun; Du, Yunfei; Liang, Zhidan; Li, Xiangke; Pan, Yan; Zhao, Kang
Simple conversion of enamines to 2H-azirines and their rearrangements under thermal conditions.
Organic letters, 2009, 11, 2643-2646
1503924 CIFC12 H18 Cl3 N O4 SP 21 21 216.7893; 10.428; 23.669
90; 90; 90		1675.74Testero, Sebastian A.; O'Daniel, Peter I; Shi, Qicun; Lee, Mijoon; Hesek, Dusan; Ishiwata, Akihiro; Noll, Bruce C.; Mobashery, Shahriar
Regiospecific syntheses of 6alpha-(1R-Hydroxyoctyl)penicillanic acid and 6beta-(1R-hydroxyoctyl)penicillanic acid as mechanistic probes of class D beta-lactamases.
Organic letters, 2009, 11, 2515-2518
1503925 CIFC24 H26 Br N O4 SP 1 21 19.2806; 9.818; 25.3589
90; 90.301; 90		2310.6Testero, Sebastian A.; O'Daniel, Peter I; Shi, Qicun; Lee, Mijoon; Hesek, Dusan; Ishiwata, Akihiro; Noll, Bruce C.; Mobashery, Shahriar
Regiospecific syntheses of 6alpha-(1R-Hydroxyoctyl)penicillanic acid and 6beta-(1R-hydroxyoctyl)penicillanic acid as mechanistic probes of class D beta-lactamases.
Organic letters, 2009, 11, 2515-2518
1503926 CIFC21 H19 Br2 N O3 SP 21 21 2110.102; 12.1513; 16.7878
90; 90; 90		2060.74Testero, Sebastian A.; O'Daniel, Peter I; Shi, Qicun; Lee, Mijoon; Hesek, Dusan; Ishiwata, Akihiro; Noll, Bruce C.; Mobashery, Shahriar
Regiospecific syntheses of 6alpha-(1R-Hydroxyoctyl)penicillanic acid and 6beta-(1R-hydroxyoctyl)penicillanic acid as mechanistic probes of class D beta-lactamases.
Organic letters, 2009, 11, 2515-2518
1503927 CIFC16 H20 O7P 1 2/c 111.269; 5.309; 12.835
90; 90.832; 90		767.8Schneider, Tobias F.; Kaschel, Johannes; Dittrich, Birger; Werz, Daniel B.
anti-Oligoannelated THF moieties: synthesis via push-pull-substituted cyclopropanes.
Organic letters, 2009, 11, 2317-2320
1503928 CIFC12 H12 O5C 2 2 216.1208; 9.984; 17.437
90; 90; 90		1065.6Schneider, Tobias F.; Kaschel, Johannes; Dittrich, Birger; Werz, Daniel B.
anti-Oligoannelated THF moieties: synthesis via push-pull-substituted cyclopropanes.
Organic letters, 2009, 11, 2317-2320
1503929 CIFC16 H16 O7F d d 242.329; 5.8139; 11.242
90; 90; 90		2766.6Schneider, Tobias F.; Kaschel, Johannes; Dittrich, Birger; Werz, Daniel B.
anti-Oligoannelated THF moieties: synthesis via push-pull-substituted cyclopropanes.
Organic letters, 2009, 11, 2317-2320
1503930 CIFC19 H22 N2 O3P -15.7503; 10.5035; 14.432
87.326; 82.357; 81.262		853.59Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503931 CIFC19 H22 N2 O3P -15.7787; 10.6482; 14.3895
86.801; 78.749; 78.606		851.16Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503932 CIFC18 H26 N2 O3P b c a9.7178; 12.0387; 29.641
90; 90; 90		3467.7Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503933 CIFC20 H24 N2 O3P 21 21 219.1658; 10.0683; 20.92
90; 90; 90		1930.6Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503934 CIFC18 H26 N2 O5P 21 21 2110.3321; 12.9156; 14.6989
90; 90; 90		1961.5Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503935 CIFC18 H26 N2 O5P 1 21 113.1001; 10.7849; 13.7862
90; 93.266; 90		1944.6Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503936 CIFC21 H26 N2 O4P 21 21 218.1499; 11.39; 21.5007
90; 90; 90		1995.9Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503937 CIFC21 H26 N2 O4P 21 21 218.5922; 15.1199; 15.2994
90; 90; 90		1987.6Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503938 CIFC20 H23 N3 O5P 1 21/n 19.3075; 16.2765; 12.9681
90; 97.095; 90		1949.54Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503939 CIFC20 H23 N3 O5P -18.266; 8.6189; 13.5928
90.56; 92.301; 97.502		959.2Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503940 CIFC20 H23 N3 O5P 1 21/c 113.0395; 14.0038; 10.7809
90; 98.343; 90		1947.8Chen, Yunfeng; Zhong, Cheng; Petersen, Jeffrey L.; Akhmedov, Novruz G.; Shi, Xiaodong
One-pot asymmetric synthesis of substituted piperidines by exocyclic chirality induction.
Organic letters, 2009, 11, 2333-2336
1503941 CIFC77 H42 Cl4 F24 O4 P4 Rh2P 21 21 214.085; 14.146; 19.443
90; 90; 90		3873.9Korenaga, Toshinobu; Osaki, Kazutaka; Maenishi, Ryota; Sakai, Takashi
Electron-poor chiral diphosphine ligands: high performance for Rh-catalyzed asymmetric 1,4-addition of arylboronic acids at room temperature.
Organic letters, 2009, 11, 2325-2328
1503942 CIFC16 H19 N O2P -15.841; 10.3833; 12.1823
68.924; 77.652; 84.613		673.35Han, Xiuling; Lu, Xiyan
Novel palladium-catalyzed acyloxylation/cyclization of 2-(3'-alkenyl)indoles.
Organic letters, 2009, 11, 2381-2384
1503943 CIFC10 H15 N5 O3P b c a6.936; 17.283; 20.657
90; 90; 90		2476.3Picon, Sylvain; Tran, Huu Dau Elise; Martin, Marie-Thérèse; Retailleau, Pascal; Zaparucha, Anne; Al-Mourabit, Ali
Biomimetically inspired short access to the 2-aminoimidazole-fused tetracyclic core of (+/-)-dibromoagelaspongin.
Organic letters, 2009, 11, 2523-2526
1503944 CIFC14 H10 Br2 D5 N5 O4P 1 21/c 111.905; 13.448; 12.532
90; 118.03; 90		1771Picon, Sylvain; Tran, Huu Dau Elise; Martin, Marie-Thérèse; Retailleau, Pascal; Zaparucha, Anne; Al-Mourabit, Ali
Biomimetically inspired short access to the 2-aminoimidazole-fused tetracyclic core of (+/-)-dibromoagelaspongin.
Organic letters, 2009, 11, 2523-2526
1503945 CIFC25 H22 O6C 1 2/c 138.18; 8.344; 14.4486
90; 108.287; 90		4370.5Wang, Kung K.; Wang, Yu-Hsuan; Yang, Hua; Akhmedov, Novruz G.; Petersen, Jeffrey L.
Synthesis of a C(56)H(40) hydrocarbon bearing a 54-carbon framework of C(60).
Organic letters, 2009, 11, 2527-2530
1503946 CIFC24 H24 O5P 1 21/c 116.5901; 6.2077; 21.518
90; 112.619; 90		2045.6Wang, Kung K.; Wang, Yu-Hsuan; Yang, Hua; Akhmedov, Novruz G.; Petersen, Jeffrey L.
Synthesis of a C(56)H(40) hydrocarbon bearing a 54-carbon framework of C(60).
Organic letters, 2009, 11, 2527-2530
1503947 CIFC40 H28 O3P 1 21/n 114.3259; 10.8416; 18.3401
90; 96.073; 90		2832.5Wang, Kung K.; Wang, Yu-Hsuan; Yang, Hua; Akhmedov, Novruz G.; Petersen, Jeffrey L.
Synthesis of a C(56)H(40) hydrocarbon bearing a 54-carbon framework of C(60).
Organic letters, 2009, 11, 2527-2530
1503948 CIFC40 H28 I2 O2P 1 21/c 111.0096; 11.961; 23.52
90; 96.074; 90		3079.9Wang, Kung K.; Wang, Yu-Hsuan; Yang, Hua; Akhmedov, Novruz G.; Petersen, Jeffrey L.
Synthesis of a C(56)H(40) hydrocarbon bearing a 54-carbon framework of C(60).
Organic letters, 2009, 11, 2527-2530
1503949 CIFC58 H40 Cl4 I2 O2P -110.2108; 14.0601; 18.1008
88.627; 88.322; 70.761		2452.2Wang, Kung K.; Wang, Yu-Hsuan; Yang, Hua; Akhmedov, Novruz G.; Petersen, Jeffrey L.
Synthesis of a C(56)H(40) hydrocarbon bearing a 54-carbon framework of C(60).
Organic letters, 2009, 11, 2527-2530
1503950 CIFC57.5 H40.5 Cl I2 OP b c n32.948; 17.014; 31.987
90; 90; 90		17931Wang, Kung K.; Wang, Yu-Hsuan; Yang, Hua; Akhmedov, Novruz G.; Petersen, Jeffrey L.
Synthesis of a C(56)H(40) hydrocarbon bearing a 54-carbon framework of C(60).
Organic letters, 2009, 11, 2527-2530
1503951 CIFC20 H25 N O2P 1 21/c 112.846; 17.476; 15.118
90; 90.186; 90		3393.9Tian, Xia; Huters, Alexander D.; Douglas, Colin J.; Garg, Neil K.
Concise synthesis of the bicyclic scaffold of N-methylwelwitindolinone C isothiocyanate via an indolyne cyclization.
Organic letters, 2009, 11, 2349-2351
1503952 CIFC20 H18 O3P 1 21/c 127.2828; 7.17088; 15.7671
90; 106.857; 90		2952.16Kuninobu, Yoichiro; Morita, Junya; Nishi, Mitsumi; Kawata, Atsushi; Takai, Kazuhiko
Rhenium-catalyzed formation of bicyclo[3.3.1]nonene frameworks by a reaction of cyclic beta-keto esters with terminal alkynes.
Organic letters, 2009, 11, 2535-2537
1503953 CIFC86 H66 Cl6 N8 O3 ZnP -112.7416; 13.0016; 23.9379
77.838; 86.008; 69.139		3622.39Lo, Mamadou; Mahajan, Dinesh; Wytko, Jennifer A.; Boudon, Corinne; Weiss, Jean
Toward generic models of hemoproteins.
Organic letters, 2009, 11, 2487-2490
1503954 CIFC18 H20 N2 O2C 1 2/c 120.4836; 4.609; 15.63
90; 97.35; 90		1463.49Xiao, Jian; Loh, Teck-Peng
Design, synthesis and optical resolution of new bifunctional ligand: 1,1'-dimethyl-octahydro-8,8'-biquinoline-7,7'-diol.
Organic letters, 2009, 11, 2876-2879
1503955 CIFC31 H42 N2 O4P 21 21 2112.3403; 14.6166; 15.2085
90; 90; 90		2743.21Xiao, Jian; Loh, Teck-Peng
Design, synthesis and optical resolution of new bifunctional ligand: 1,1'-dimethyl-octahydro-8,8'-biquinoline-7,7'-diol.
Organic letters, 2009, 11, 2876-2879
1503956 CIFC15 H23 B O2P -19.4826; 11.5606; 14.2207
68.11; 78.325; 84.522		1416.27Erdyakov, Sergey Yu; Ignatenko, Anatolii V.; Potapova, Tamara V.; Lyssenko, Konstantin A.; Gurskii, Mikhail E.; Bubnov, Yuri N.
Design of bicyclic and cage boron compounds based on allylboration of acetylenes with allyldichloroboranes.
Organic letters, 2009, 11, 2872-2875
1503957 CIFC20 H34 B NP -111.2017; 13.174; 13.299
66.3; 79.906; 72.084		1706.9Erdyakov, Sergey Yu; Ignatenko, Anatolii V.; Potapova, Tamara V.; Lyssenko, Konstantin A.; Gurskii, Mikhail E.; Bubnov, Yuri N.
Design of bicyclic and cage boron compounds based on allylboration of acetylenes with allyldichloroboranes.
Organic letters, 2009, 11, 2872-2875
1503958 CIFC74 H102 Cl6 O4 S8P -113.756; 16.679; 19.491
97.186; 107.111; 107.699		3957.1Chen, Guang; Dawe, Louise; Wang, Li; Zhao, Yuming
Planar acetylene-expanded TTFAQ analogues.
Organic letters, 2009, 11, 2736-2739
1503959 CIFC31 H30 F6 N2 O3P 1 21 19.5388; 14.56; 10.9484
90; 109.057; 90		1437.23Wen, Yuehong; Zhao, Baoguo; Shi, Yian
Cu(I)-catalyzed diamination of disubstituted terminal olefins: an approach to potent NK1 antagonist.
Organic letters, 2009, 11, 2365-2368
1503960 CIFC12 H6 Se3P 1 21/c 19.079; 11.625; 11.712
90; 112.694; 90		1140.4Kashiki, Tomoya; Shinamura, Shoji; Kohara, Masahiro; Miyazaki, Eigo; Takimiya, Kazuo; Ikeda, Masaaki; Kuwabara, Hirokazu
One-pot synthesis of benzo[b]thiophenes and benzo[b]selenophenes from o-halo-substituted ethynylbenzenes: convenient approach to mono-, bis-, and tris-chalcogenophene-annulated benzenes.
Organic letters, 2009, 11, 2473-2475
1503961 CIFC24 H50 O5 Si4C 1 2 125.1341; 9.5269; 16.8986
90; 128.434; 90		3169.6Bower, Justin; Box, Matthew R.; Czyzewski, Michal; Goeta, Andres E.; Steel, Patrick G.
Acyl polysilanes: new acyl anion equivalents for additions to electron-deficient alkenes.
Organic letters, 2009, 11, 2744-2747
1503962 CIFC15 H16 Cl3 N O5P 21 21 219.4608; 13.0758; 14.0284
90; 90; 90		1735.42Gromov, Alexey; Enev, Valentin; Mulzer, Johann
A desymmetrization approach toward highly oxygenated cis-decalins.
Organic letters, 2009, 11, 2884-2886
1503963 CIFC20 H24 O5P 21 21 216.9194; 7.8312; 30.9251
90; 90; 90		1675.74Gromov, Alexey; Enev, Valentin; Mulzer, Johann
A desymmetrization approach toward highly oxygenated cis-decalins.
Organic letters, 2009, 11, 2884-2886
1503964 CIFC21 H21 SP -17.7299; 9.2123; 12.422
69.112; 81.845; 85.655		817.8Wang, Jing; Liu, Ke; Liu, Yi-Yang; Song, Cheng-Li; Shi, Zi-Fa; Peng, Jun-Biao; Zhang, Hao-Li; Cao, Xiao-Ping
New oligothiophene-pentacene hybrids as highly stable and soluble organic semiconductors.
Organic letters, 2009, 11, 2563-2566
1503965 CIFC14 H17 N O2P 21 21 219.7999; 10.2406; 11.7764
90; 90; 90		1181.84Zoute, Ludivine; Kociok-Köhn, Gabriele; Frost, Christopher G.
Rhodium-catalyzed 1,4-additions to enantiopure acceptors: asymmetric synthesis of functionalized pyrrolizidinones.
Organic letters, 2009, 11, 2491-2494
1503966 CIFC62 H50 N4 O10P -113.711; 13.7756; 14.9349
97.877; 95.04; 92.744		2778.3She, Nengfang; Gao, Meng; Cao, Liping; Wu, Anxin; Isaacs, Lyle
Sensor for nitrophenol based on a fluorescent molecular clip.
Organic letters, 2009, 11, 2603-2606
1503967 CIFC24 H30 N2 O3P 21 21 219.5509; 11.1823; 20.0306
90; 90; 90		2139.29Wanner, Martin J.; Boots, Rowan N. A.; Eradus, Bram; de Gelder, René; van Maarseveen, Jan H.; Hiemstra, Henk
Organocatalytic enantioselective total synthesis of (-)-arboricine.
Organic letters, 2009, 11, 2579-2581
1503968 CIFC12 H14 N2 O2P 1 c 111.2189; 11.3198; 8.7223
90; 92.1671; 90		1106.9Oakdale, James S.; Solano, Danielle M.; Fettinger, James C.; Haddadin, Makhluf J.; Kurth, Mark J.
An oxazolo[3,2-b]indazole route to 1H-indazolones.
Organic letters, 2009, 11, 2760-2763
1503969 CIFC44 H48 SP -110.481; 12.266; 13.619
101.824; 93.497; 91.387		1709.3Ni, Yang; Nakajima, Kiyohiko; Kanno, Ken-ichiro; Takahashi, Tamotsu
Zirconium-mediated coupling reaction for synthesis of substituted thiophene-fused acenes.
Organic letters, 2009, 11, 3702-3705
1503970 CIFC38 H50 S Si2P 1 21/c 110.052; 17.403; 20.696
90; 99.771; 90		3568Ni, Yang; Nakajima, Kiyohiko; Kanno, Ken-ichiro; Takahashi, Tamotsu
Zirconium-mediated coupling reaction for synthesis of substituted thiophene-fused acenes.
Organic letters, 2009, 11, 3702-3705
1503971 CIFC14 H15 N O3P 1 21/c 16.2715; 11.4983; 34.248
90; 90.731; 90		2469.48Chen, Guofei; Fu, Chunling; Ma, Shengming
A novel synthesis of 1,3-oxazine-2,4-diones via a simple and efficient reaction of CO2 with 2,3-allenamides.
Organic letters, 2009, 11, 2900-2903
1503972 CIFC20 H24 O4P 21 21 217.711; 10.5025; 20.8344
90; 90; 90		1687.27Majetich, George; Grove, Jeremy L.
Total synthesis of (+)-19-deoxyicetexone, (-)-icetexone, and (+)-5-epi-icetexone.
Organic letters, 2009, 11, 2904-2907
1503973 CIFC20 H22 O5P 21 21 217.747; 10.338; 20.948
90; 90; 90		1677.7Majetich, George; Grove, Jeremy L.
Total synthesis of (+)-19-deoxyicetexone, (-)-icetexone, and (+)-5-epi-icetexone.
Organic letters, 2009, 11, 2904-2907
1503974 CIFC20 H22 O5P c a 2112.306; 12.827; 10.576
90; 90; 90		1669.4Majetich, George; Grove, Jeremy L.
Total synthesis of (+)-19-deoxyicetexone, (-)-icetexone, and (+)-5-epi-icetexone.
Organic letters, 2009, 11, 2904-2907
1503975 CIFC73.8 H12.9 N2 O6.3 S2.4P -114.0617; 17.0906; 19.3399
90.8266; 104.694; 94.1097		4481.69Zhang, Qianyan; Jia, Zhenshan; Liu, Shuming; Zhang, Gang; Xiao, Zuo; Yang, Dazhi; Gan, Liangbing; Wang, Zheming; Li, Yuliang
Efficient cage-opening cascade process for the preparation of water-encapsulated [60]fullerene derivatives.
Organic letters, 2009, 11, 2772-2774
1503976 CIFC73.8 H13.64 N2 O6.67 S2.4P -114.059; 17.0748; 19.3384
90.9325; 104.735; 94.0137		4475.79Zhang, Qianyan; Jia, Zhenshan; Liu, Shuming; Zhang, Gang; Xiao, Zuo; Yang, Dazhi; Gan, Liangbing; Wang, Zheming; Li, Yuliang
Efficient cage-opening cascade process for the preparation of water-encapsulated [60]fullerene derivatives.
Organic letters, 2009, 11, 2772-2774
1503977 CIFC24 H21 N O4 S2P 21 21 218.0696; 11.8879; 22.2809
90; 90; 90		2137.42Spitz, Cédric; Lohier, Jean-François; Reboul, Vincent; Metzner, Patrick
Catalytic generation of cesium acetylide by CsF: synthesis of 1,3-benzothiazines from cyclic sulfenamides.
Organic letters, 2009, 11, 2776-2779
1503978 CIFC26 H27 N O4 S3P 1 21 17.9756; 12.987; 11.917
90; 95.938; 90		1227.7Spitz, Cédric; Lohier, Jean-François; Reboul, Vincent; Metzner, Patrick
Catalytic generation of cesium acetylide by CsF: synthesis of 1,3-benzothiazines from cyclic sulfenamides.
Organic letters, 2009, 11, 2776-2779
1503979 CIFC19 H14 N2 O6P 1 21/c 114.8521; 9.1835; 13.5407
90; 112.831; 90		1702.18Rasberry, Roger D.; Wu, Xiangyang; Bullock, Brooke N.; Smith, Mark D.; Shimizu, Ken D.
A small molecule diacid with long-term chiral memory.
Organic letters, 2009, 11, 2599-2602
1503980 CIFC17 H18 Cl N O6P 1 21/a 111.5118; 8.8192; 17.5093
90; 105.927; 90		1709.4Yamazaki, Shoko; Morikawa, Satoshi; Miyazaki, Kazuya; Takebayashi, Masachika; Yamamoto, Yuko; Morimoto, Tsumoru; Kakiuchi, Kiyomi; Mikata, Yuji
Zinc-catalyzed reactions of ethenetricarboxylates with 2-(trimethylsilylethynyl)anilines leading to bridged quinoline derivatives.
Organic letters, 2009, 11, 2796-2799
1503981 CIFC18 H16 N2 O6P -19.6009; 9.9357; 10.035
95.531; 96.755; 110.311		881.8Liang, Jixuan; Chen, Jingbo; Du, Fengxiang; Zeng, Xianghui; Li, Liang; Zhang, Hongbin
Oxidative carbon-carbon bond formation in the synthesis of bioactive spiro beta-lactams.
Organic letters, 2009, 11, 2820-2823
1503982 CIFC5 H10 N2 O2P 21 21 216.93904; 8.06968; 10.42331
90; 90; 90		583.66Sharma, Rojita; Bulger, Paul G.; McNevin, Michael; Dormer, Peter G.; Ball, Richard G.; Streckfuss, Eric; Cuff, James F.; Yin, Jingjun; Chen, Cheng-yi
A cascade approach to cyclic aminonitrones: reaction discovery, mechanism, and scope.
Organic letters, 2009, 11, 3194-3197
1503983 CIFC11 H20 N2 O2P c c n20.5261; 12.69158; 9.48439
90; 90; 90		2470.77Sharma, Rojita; Bulger, Paul G.; McNevin, Michael; Dormer, Peter G.; Ball, Richard G.; Streckfuss, Eric; Cuff, James F.; Yin, Jingjun; Chen, Cheng-yi
A cascade approach to cyclic aminonitrones: reaction discovery, mechanism, and scope.
Organic letters, 2009, 11, 3194-3197
1503984 CIFC19 H21 N O5P 1 21/n 17.8324; 25.8462; 8.3639
90; 107.473; 90		1615.04Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503985 CIFC19 H18 N2 O3P 1 21/c 19.9933; 8.1292; 19.993
90; 103.468; 90		1579.5Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503986 CIFC22 H21 N O3P 1 21/c 111.9736; 13.2421; 11.3948
90; 102.494; 90		1763.92Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503987 CIFC18 H19 N O5C 1 c 112.049; 15.856; 8.11
90; 96.293; 90		1540.1Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503988 CIFC18 H16 N2 O3P 1 21/c 124.45; 8.5899; 6.914
90; 95.112; 90		1446.3Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503989 CIFC18 H21 N O5P b c a12.7255; 9.7373; 26.8842
90; 90; 90		3331.3Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503990 CIFC20 H23 N O5P 21 21 217.4009; 9.1172; 26.7217
90; 90; 90		1803.06Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503991 CIFC19 H21 N O5P 1 21/c 114.7842; 14.5452; 7.6305
90; 102.909; 90		1599.39Tang, Yuchen; Fettinger, James C.; Shaw, Jared T.
One-step synthesis of complex nitrogen heterocycles from imines and alkyl-substituted maleic anhydrides.
Organic letters, 2009, 11, 3802-3805
1503992 CIFC36 H29 N O2 SC 1 2/c 121.5239; 10.7271; 26.8898
90; 113.017; 90		5714.3Wang, Shaoyin; Zhu, Yuanxun; Wang, Yanguang; Lu, Ping
Synthesis of functionalized indenes via cascade reaction of aziridines and propargyl alcohols.
Organic letters, 2009, 11, 2615-2618
1503993 CIFC36 H31 N O3 SP 1 21/c 114.1643; 10.301; 20.838
90; 103.915; 90		2951.2Wang, Shaoyin; Zhu, Yuanxun; Wang, Yanguang; Lu, Ping
Synthesis of functionalized indenes via cascade reaction of aziridines and propargyl alcohols.
Organic letters, 2009, 11, 2615-2618
1503994 CIFC36 H29 N O2 SP -110.4922; 11.4291; 12.9158
88.416; 70.878; 84.564		1456.8Wang, Shaoyin; Zhu, Yuanxun; Wang, Yanguang; Lu, Ping
Synthesis of functionalized indenes via cascade reaction of aziridines and propargyl alcohols.
Organic letters, 2009, 11, 2615-2618
1503995 CIFC29 H20P -18.8382; 9.7835; 12.0361
77.648; 76.495; 79.917		979.93Wang, Shaoyin; Zhu, Yuanxun; Wang, Yanguang; Lu, Ping
Synthesis of functionalized indenes via cascade reaction of aziridines and propargyl alcohols.
Organic letters, 2009, 11, 2615-2618
1503996 CIFC36 H27 N O2 SP 1 21/c 113.9715; 12.9265; 16.0665
90; 105.422; 90		2797.2Wang, Shaoyin; Zhu, Yuanxun; Wang, Yanguang; Lu, Ping
Synthesis of functionalized indenes via cascade reaction of aziridines and propargyl alcohols.
Organic letters, 2009, 11, 2615-2618
1503997 CIFC33 H35 Cl O11P 21 21 2111.528; 16.331; 16.484
90; 90; 90		3103.3Liu, Ling; Li, Yan; Liu, Shuchun; Zheng, Zhihui; Chen, Xulin; Zhang, Hua; Guo, Liangdong; Che, Yongsheng
Chloropestolide A, an antitumor metabolite with an unprecedented spiroketal skeleton from Pestalotiopsis fici.
Organic letters, 2009, 11, 2836-2839
1503998 CIFC54 H74 Cl6 O4 Se4I 41/a :228.2866; 28.2866; 14.7993
90; 90; 90		11841.4Thomas, Joice; Maes, Wouter; Robeyns, Koen; Ovaere, Margriet; Van Meervelt, Luc; Smet, Mario; Dehaen, Wim
Homoselenacalix[n]arenes.
Organic letters, 2009, 11, 3040-3043
1503999 CIFC78 H108 O6 Se6P -19.9877; 12.0647; 15.8791
83.135; 88.746; 87.532		1897.66Thomas, Joice; Maes, Wouter; Robeyns, Koen; Ovaere, Margriet; Van Meervelt, Luc; Smet, Mario; Dehaen, Wim
Homoselenacalix[n]arenes.
Organic letters, 2009, 11, 3040-3043
1504000 CIFC42 H26 Br2 N4 NiP -19.948; 12.8818; 14.3014
70.874; 73.322; 80.864		1654.4Li, Ke-Lai; Guo, Can-Cheng; Chen, Qing-Yun
Unprecedented degradation of nickel(II) 2,3,12,13-tetrabromo-5,10,15,20-tetraarylporphyrins by the anion of E-benzaldoxime: a novel approach to nickel(II) chlorophins and bacteriophins.
Organic letters, 2009, 11, 2724-2727
1504001 CIFC44 H32 Br N4 Ni O0.5P 1 21/n 115.775; 12.4675; 17.5806
90; 93.757; 90		3450.2Li, Ke-Lai; Guo, Can-Cheng; Chen, Qing-Yun
Unprecedented degradation of nickel(II) 2,3,12,13-tetrabromo-5,10,15,20-tetraarylporphyrins by the anion of E-benzaldoxime: a novel approach to nickel(II) chlorophins and bacteriophins.
Organic letters, 2009, 11, 2724-2727
1504002 CIFC77 H97 N5 NiC c c a :227.77; 35.78; 8.445
90; 90; 90		8391Li, Ke-Lai; Guo, Can-Cheng; Chen, Qing-Yun
Unprecedented degradation of nickel(II) 2,3,12,13-tetrabromo-5,10,15,20-tetraarylporphyrins by the anion of E-benzaldoxime: a novel approach to nickel(II) chlorophins and bacteriophins.
Organic letters, 2009, 11, 2724-2727
1504003 CIFC17 H19 Br O3P 21 21 219.5718; 12.1385; 14.436
90; 90; 90		1677.3Liu, Yan-kai; Ma, Chao; Jiang, Kun; Liu, Tian-Yu; Chen, Ying-Chun
Asymmetric tandem Michael addition-Wittig reaction to cyclohexenone annulation.
Organic letters, 2009, 11, 2848-2851
1504004 CIFC22 H27 N O5P 1 21 19.082; 11.525; 10.141
90; 104.82; 90		1026.1Gallier, Florian; Hussain, Hidayat; Martel, Arnaud; Kirschning, Andreas; Dujardin, Gilles
Hetero-Diels-Alder reactions of cyclic ketone derived enamide. A new and efficient concept for the asymmetric Robinson annulation.
Organic letters, 2009, 11, 3060-3063
1504005 CIFC10 H6 O S2P 21 21 219.43737; 16.8839; 5.68402
90; 90; 90		905.69Henssler, John T.; Matzger, Adam J.
Facile and scalable synthesis of the fused-ring heterocycles thieno[3,2-b]thiophene and thieno[3,2-b]furan.
Organic letters, 2009, 11, 3144-3147
1504006 CIFC9 H9 N3I 41/a :216.9796; 16.9796; 11.4331
90; 90; 90		3296.24Liang, Lei; Li, Zhengkai; Zhou, Xiangge
Pyridine N-oxides as ligands in Cu-catalyzed N-arylation of imidazoles in water.
Organic letters, 2009, 11, 3294-3297
1504007 CIFC28 H20 Cl2 N6 O4P 1 21/a 17.518; 27.568; 12.404
90; 105.52; 90		2477.1Sinan, Mominul; Panda, Manashi; Banerjee, Priyabrata; Shinisha, C. B.; Sunoj, Raghavan B.; Goswami, Sreebrata
Synthesis of azoaromatic dyes via redox driven C-N bond fusion.
Organic letters, 2009, 11, 3218-3221
1504008 CIFC90 H85 N11 O8P -113.5021; 15.7541; 18.9376
70.524; 88.842; 77.787		3706.3Wagner, Gerald; Arion, Vladimir B.; Brecker, Lothar; Krantz, Carsten; Mieusset, Jean-Luc; Brinker, Udo H.
Controllable selective functionalization of a cavitand via solid state photolysis of an encapsulated phenyl azide.
Organic letters, 2009, 11, 3056-3058
1504009 CIFC10 H20 O4P 1 21/c 112.9287; 10.867; 8.3246
90; 104.587; 90		1131.87Duplessis, Martin; Waltz, Marie-Eve; Bencheqroun, Mohammed; Cardinal-David, Benoit; Guindon, Yvan
Stereoselective quaternary center construction via atom-transfer radical cyclization using silicon tethers on acyclic precursors.
Organic letters, 2009, 11, 3148-3151
1504010 CIFC18 H23 N O6P -16.1407; 7.3149; 21.3626
87.205; 86.658; 72.179		911.5Duplessis, Martin; Waltz, Marie-Eve; Bencheqroun, Mohammed; Cardinal-David, Benoit; Guindon, Yvan
Stereoselective quaternary center construction via atom-transfer radical cyclization using silicon tethers on acyclic precursors.
Organic letters, 2009, 11, 3148-3151
1504011 CIFC9 H16 O4P 21 21 216.2529; 8.6287; 18.3445
90; 90; 90		989.77Duplessis, Martin; Waltz, Marie-Eve; Bencheqroun, Mohammed; Cardinal-David, Benoit; Guindon, Yvan
Stereoselective quaternary center construction via atom-transfer radical cyclization using silicon tethers on acyclic precursors.
Organic letters, 2009, 11, 3148-3151
1504012 CIFC20 H17 N S2P b c a9.6873; 17.8299; 18.963
90; 90; 90		3275.4Balaji, Ganapathy; Valiyaveettil, Suresh
Synthesis and properties of symmetric and unsymmetric dibenzothienopyrroles.
Organic letters, 2009, 11, 3358-3361
1504013 CIFC28 H25 N S2P -18.3728; 11.6125; 12.365
102.462; 100.036; 102.883		1112.69Balaji, Ganapathy; Valiyaveettil, Suresh
Synthesis and properties of symmetric and unsymmetric dibenzothienopyrroles.
Organic letters, 2009, 11, 3358-3361
1504014 CIFC28 H25 N S2P -110.4421; 11.0184; 11.3293
81.712; 68.121; 66.569		1109.85Balaji, Ganapathy; Valiyaveettil, Suresh
Synthesis and properties of symmetric and unsymmetric dibenzothienopyrroles.
Organic letters, 2009, 11, 3358-3361
1504015 CIFC23 H21 Br N2 O4 SP 21 21 219.951; 10.141; 22.1
90; 90; 90		2230.2Wang, Xiao; Chen, Yong-Fei; Niu, Liang-Feng; Xu, Peng-Fei
Diastereo- and enantioselective Aza-MBH-type reaction of nitroalkenes to N-tosylimines catalyzed by bifunctional organocatalysts.
Organic letters, 2009, 11, 3310-3313
1504016 CIFC32 H28 O3P -19.372; 10.346; 13.724
68.111; 84.53; 76.94		1202.8Zhang, Hongyu; Karasawa, Takashi; Yamada, Hiroshi; Wakamiya, Atsushi; Yamaguchi, Shigehiro
Intramolecular reductive double cyclization of o,o'-bis(arylcarbonyl)diphenylacetylenes: synthesis of ladder pi-conjugated skeletons.
Organic letters, 2009, 11, 3076-3079
1504017 CIFC28 H20 O2P 1 21 18.94; 10.89; 10.079
90; 95.4352; 90		976.8Zhang, Hongyu; Karasawa, Takashi; Yamada, Hiroshi; Wakamiya, Atsushi; Yamaguchi, Shigehiro
Intramolecular reductive double cyclization of o,o'-bis(arylcarbonyl)diphenylacetylenes: synthesis of ladder pi-conjugated skeletons.
Organic letters, 2009, 11, 3076-3079
1504018 CIFC43 H31 Cl3 O2P 1 21/c 117.962; 9.9317; 20.157
90; 112.669; 90		3318.1Zhang, Hongyu; Karasawa, Takashi; Yamada, Hiroshi; Wakamiya, Atsushi; Yamaguchi, Shigehiro
Intramolecular reductive double cyclization of o,o'-bis(arylcarbonyl)diphenylacetylenes: synthesis of ladder pi-conjugated skeletons.
Organic letters, 2009, 11, 3076-3079
1504019 CIFC49 H44 Cl2 N2 O5P 1 21/n 18.5797; 33.294; 15.726
90; 103.6; 90		4366.2Zhen, Yonggang; Qian, Hualei; Xiang, Junfeng; Qu, Jianqiang; Wang, Zhaohui
Highly regiospecific synthetic approach to monobay-functionalized perylene bisimide and di(perylene bisimide).
Organic letters, 2009, 11, 3084-3087
1504020 CIFC23 H28 OP -19.769; 14.36; 14.469
71.8; 88.188; 70.926		1816.7Saadi, Jakub; Lentz, Dieter; Reissig, Hans-Ulrich
Medium-sized carbocycles by samarium diiodide-induced carbonyl-alkene cyclizations.
Organic letters, 2009, 11, 3334-3337
1504021 CIFC24 H30 O3C 1 c 18.4941; 15.472; 15.68
90; 104.415; 90		1995.8Saadi, Jakub; Lentz, Dieter; Reissig, Hans-Ulrich
Medium-sized carbocycles by samarium diiodide-induced carbonyl-alkene cyclizations.
Organic letters, 2009, 11, 3334-3337
1504022 CIFC57 H59 N3 O3 S6P -19.4516; 11.37; 24.6642
86.345; 84.729; 81.128		2604.43Jaggi, Michael; Blum, Carmen; Dupont, Nathalie; Grilj, Jakob; Liu, Shi-Xia; Hauser, Jürg; Hauser, Andreas; Decurtins, Silvio
A compactly fused pi-conjugated tetrathiafulvalene-perylenediimide donor-acceptor dyad.
Organic letters, 2009, 11, 3096-3099
1504023 CIFC18 H24 I N O2 SP 1 21 110.8791; 9.4754; 18.4279
90; 99.751; 90		1872.17Biradar, Deepak B.; Zhou, Shuangliu; Gau, Han-Mou
Direct asymmetric catalytic thienylaluminum addition to ketones: a concise approach to the synthesis of (S)-tiemonium iodide.
Organic letters, 2009, 11, 3386-3389
1504024 CIFC29 H23 N6 O PP -18.7372; 9.6953; 16.196
73.121; 82.282; 64.087		1180.8Matano, Yoshihiro; Nakashima, Makoto; Saito, Arihiro; Imahori, Hiroshi
Phosphole-triazole hybrids: a facile synthesis and complexation with Pd(II) and Pt(II) salts.
Organic letters, 2009, 11, 3338-3341
1504025 CIFC31 H26 Cl10 N3 P PdP -18.1743; 13.1609; 17.591
80.241; 76.545; 84.462		1810.7Matano, Yoshihiro; Nakashima, Makoto; Saito, Arihiro; Imahori, Hiroshi
Phosphole-triazole hybrids: a facile synthesis and complexation with Pd(II) and Pt(II) salts.
Organic letters, 2009, 11, 3338-3341
1504026 CIFC19 H25 N3 O3P 1 21/n 111.4263; 18.5145; 26.0098
90; 93.217; 90		5493.76Shaabani, Ahmad; Rezayan, Ali Hossein; Keshipour, Sajjad; Sarvary, Afshin; Ng, Seik Weng
A novel one-pot three-(in situ five-)component condensation reaction: an unexpected approach for the synthesis of tetrahydro-2,4-dioxo-1H-benzo[b][1,5]diazepine-3-yl-2-methylpropanamide derivatives.
Organic letters, 2009, 11, 3342-3345
1504027 CIFC15 H17 N O2P 21 21 217.8567; 11.2624; 14.7834
90; 90; 90		1308.11Castaldi, M. Paola; Troast, Dawn M.; Porco, Jr, John A
Stereoselective synthesis of spirocyclic oxindoles via Prins cyclizations.
Organic letters, 2009, 11, 3362-3365
1504028 CIFC22 H23 N O3P 1 21 18.361; 8.6154; 12.8252
90; 97.499; 90		915.94Castaldi, M. Paola; Troast, Dawn M.; Porco, Jr, John A
Stereoselective synthesis of spirocyclic oxindoles via Prins cyclizations.
Organic letters, 2009, 11, 3362-3365
1504029 CIFC29 H25 Br F N O3P 1 21 110.6456; 8.2771; 13.6743
90; 96.302; 90		1197.63Castaldi, M. Paola; Troast, Dawn M.; Porco, Jr, John A
Stereoselective synthesis of spirocyclic oxindoles via Prins cyclizations.
Organic letters, 2009, 11, 3362-3365
1504030 CIFC15 H17 N O2P 21 21 217.6811; 8.0373; 20.7516
90; 90; 90		1281.11Zhang, Yun; Panek, James S.
Stereocontrolled synthesis of spirooxindoles through Lewis acid-promoted [5 + 2]-annulation of chiral silyl alcohols.
Organic letters, 2009, 11, 3366-3369
1504031 CIFC15 H17 N O2P 1 21 18.5555; 7.8352; 9.566
90; 100.67; 90		630.16Zhang, Yun; Panek, James S.
Stereocontrolled synthesis of spirooxindoles through Lewis acid-promoted [5 + 2]-annulation of chiral silyl alcohols.
Organic letters, 2009, 11, 3366-3369
1504032 CIFC15 H16 Br N O2P 21 21 219.0322; 10.4795; 29.1191
90; 90; 90		2756.2Zhang, Yun; Panek, James S.
Stereocontrolled synthesis of spirooxindoles through Lewis acid-promoted [5 + 2]-annulation of chiral silyl alcohols.
Organic letters, 2009, 11, 3366-3369
1504033 CIFC22 H23 N O2P 21 21 216.7633; 10.5401; 24.4877
90; 90; 90		1745.63Zhang, Yun; Panek, James S.
Stereocontrolled synthesis of spirooxindoles through Lewis acid-promoted [5 + 2]-annulation of chiral silyl alcohols.
Organic letters, 2009, 11, 3366-3369
1504034 CIFC36 H52 O12P -17.0217; 11.5023; 12.3086
113.451; 94.599; 97.882		893.4Li, Shijun; Liu, Ming; Zheng, Bo; Zhu, Kelong; Wang, Feng; Li, Ning; Zhao, Xiao-Li; Huang, Feihe
Taco complex templated syntheses of a cryptand/paraquat [2]rotaxane and a [2]catenane by olefin metathesis.
Organic letters, 2009, 11, 3350-3353
1504035 CIFC70 H79 F24 N4 O12 P4P -113.3566; 13.8761; 26.4176
77.624; 84.73; 78.959		4687.3Li, Shijun; Liu, Ming; Zheng, Bo; Zhu, Kelong; Wang, Feng; Li, Ning; Zhao, Xiao-Li; Huang, Feihe
Taco complex templated syntheses of a cryptand/paraquat [2]rotaxane and a [2]catenane by olefin metathesis.
Organic letters, 2009, 11, 3350-3353
1504036 CIFC24 H22 N2 O6P -19.9987; 10.4124; 11.1163
102.951; 104.668; 104.178		1033.75Bakthadoss, Manickam; Sivakumar, Govindan; Kannan, Damodharan
Solid-state melt reaction for the domino process: highly efficient synthesis of fused tetracyclic chromenopyran pyrimidinediones using Baylis-Hillman derivatives.
Organic letters, 2009, 11, 4466-4469
1504037 CIFC23 H19 N3 O4P 1 21/n 111.8479; 11.238; 14.6655
90; 98.437; 90		1931.5Bakthadoss, Manickam; Sivakumar, Govindan; Kannan, Damodharan
Solid-state melt reaction for the domino process: highly efficient synthesis of fused tetracyclic chromenopyran pyrimidinediones using Baylis-Hillman derivatives.
Organic letters, 2009, 11, 4466-4469
1504038 CIFC8 H6 Cl IP 17.352; 7.365; 16.241
91.31; 91.52; 99.58		866.5Pawluć, Piotr; Hreczycho, Grzegorz; Szudkowska, Justyna; Kubicki, Maciej; Marciniec, Bogdan
New one-pot synthesis of (E)-beta-aryl vinyl halides from styrenes.
Organic letters, 2009, 11, 3390-3393
1504039 CIFC8 H6 Br IP c c 27.2421; 20.322; 5.8538
90; 90; 90		861.53Pawluć, Piotr; Hreczycho, Grzegorz; Szudkowska, Justyna; Kubicki, Maciej; Marciniec, Bogdan
New one-pot synthesis of (E)-beta-aryl vinyl halides from styrenes.
Organic letters, 2009, 11, 3390-3393
1504040 CIFC14 H11 IP c a 2126.395; 12.0508; 7.482
90; 90; 90		2379.9Pawluć, Piotr; Hreczycho, Grzegorz; Szudkowska, Justyna; Kubicki, Maciej; Marciniec, Bogdan
New one-pot synthesis of (E)-beta-aryl vinyl halides from styrenes.
Organic letters, 2009, 11, 3390-3393
1504041 CIFC41 H40 Fe N2 O P2P 21 21 219.7307; 10.9784; 33.3226
90; 90; 90		3559.8Wang, Dao-Yong; Hu, Xiang-Ping; Hou, Chuan-Jin; Deng, Jun; Yu, Sai-Bo; Duan, Zheng-Chao; Huang, Jia-Di; Zheng, Zhuo
Enantioselective Rh-catalyzed hydrogenation of 3-aryl-2-phosphonomethylpropenoates by a new class of chiral ferrocenyl diphosphine ligands.
Organic letters, 2009, 11, 3226-3229
1504042 CIFC26 H25 NP 1 21/n 110.543; 11.806; 16.085
90; 95.6; 90		1993Gou, Fa-Rong; Huo, Peng-Fei; Bi, Hai-Peng; Guan, Zheng-Hui; Liang, Yong-Min
One-pot synthesis of highly substituted aromatic amine derivatives via Pd-catalyzed aminobenzannulation reaction.
Organic letters, 2009, 11, 3418-3421
1504043 CIFC15 H14 N2 O5 SP 1 21/c 112.1557; 12.1854; 10.5038
90; 106.703; 90		1490.2Lohse, Andrew G.; Hsung, Richard P.
Thermal intramolecular [4 + 2] cycloadditions of allenamides: a stereoselective tandem propargyl amide isomerization-cycloaddition.
Organic letters, 2009, 11, 3430-3433
1504044 CIFC13 H11 N O5P 21 21 216.3632; 11.501; 16.661
90; 90; 90		1219.3Tan, Qitao; Hayashi, Masahiko
Asymmetric desymmetrization of 4,5-epoxycyclohex-1-ene by enantioselective allylic oxidation.
Organic letters, 2009, 11, 3314-3317
1504045 CIFC18 H14 Cl F3 O2P 1 21 16.2698; 7.4785; 17.432
90; 95.01; 90		814.2Wang, Xiao-Na; Shao, Pan-Lin; Lv, Hui; Ye, Song
Enantioselective synthesis of beta-trifluoromethyl-beta-lactones via NHC-catalyzed ketene-ketone cycloaddition reactions.
Organic letters, 2009, 11, 4029-4031
1504046 CIFC16 H25 N O2 SP 1 c 16.119; 13.231; 20.15
90; 91.94; 90		1630Wang, Bing; Wang, Yong-Jun
SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism.
Organic letters, 2009, 11, 3410-3413
1504047 CIFC13 H29 N O3 SP 21 21 216.252; 14.188; 18.445
90; 90; 90		1636.1Wang, Bing; Wang, Yong-Jun
SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism.
Organic letters, 2009, 11, 3410-3413
1504048 CIFC14 H31 N O3 SP 21 21 216.51; 14.258; 18.556
90; 90; 90		1722.4Wang, Bing; Wang, Yong-Jun
SmI2-promoted intramolecular asymmetric pinacol-type ketone-tert-butanesulfinyl imine reductive coupling: stereoselectivity and mechanism.
Organic letters, 2009, 11, 3410-3413
1504049 CIFC42 H42 N6 O5C 1 2/c 124.171; 9.0645; 19.641
90; 123.943; 90		3570Li, Guo-You; Yang, Tao; Luo, Ying-Gang; Chen, Xiao-Zhen; Fang, Dong-Mei; Zhang, Guo-Lin
Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor.
Organic letters, 2009, 11, 3714-3717
1504050 CIFC18 H15 N3 O3P 1 21 17.912; 7.392; 14.05
90; 104.92; 90		794Li, Guo-You; Yang, Tao; Luo, Ying-Gang; Chen, Xiao-Zhen; Fang, Dong-Mei; Zhang, Guo-Lin
Brevianamide J, a new indole alkaloid dimer from fungus Aspergillus versicolor.
Organic letters, 2009, 11, 3714-3717
1504051 CIFC17 H28 Cl N2 RhP 1 21/n 16.5715; 18.7963; 13.799
90; 94.439; 90		1699.3Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon
A new route to acyclic diaminocarbenes via lithium-halogen exchange.
Organic letters, 2009, 11, 3274-3277
1504052 CIFC17 H28 Cl Ir N2P 1 21/c 19.8235; 14.9332; 23.221
90; 91.616; 90		3405.1Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon
A new route to acyclic diaminocarbenes via lithium-halogen exchange.
Organic letters, 2009, 11, 3274-3277
1504053 CIFC13 H22 Cl Ir N2P 21 21 217.277; 12.449; 15.738
90; 90; 90		1425.7Snead, David R.; Ghiviriga, Ion; Abboud, Khalil A.; Hong, Sukwon
A new route to acyclic diaminocarbenes via lithium-halogen exchange.
Organic letters, 2009, 11, 3274-3277
1504054 CIFC22 H16 Br N OP 21 21 216.195; 7.802; 35.452
90; 90; 90		1713.5Li, Yi; Shi, Fu-Qiang; He, Qing-Li; You, Shu-Li
N-heterocyclic carbene-catalyzed cross-coupling of aldehydes with arylsulfonyl indoles.
Organic letters, 2009, 11, 3182-3185
1504055 CIFC11 H17 N O3P -16.6599; 9.8956; 9.9738
108.604; 96.856; 97.248		609.01Meyers, Marvin J.; Muizebelt, Inouk; van Wiltenburg, Jim; Brown, David L.; Thorarensen, Atli
Synthesis of tert-butyl 6-oxo-2-azaspiro[3.3]heptane-2-carboxylate.
Organic letters, 2009, 11, 3523-3525
1504056 CIFC66 H66P 1 21/c 115.0858; 17.9286; 17.9396
90; 94.962; 90		4833.9Zhai, Linyi; Shukla, Ruchi; Rathore, Rajendra
Oxidative C-C bond formation (Scholl reaction) with DDQ as an efficient and easily recyclable oxidant.
Organic letters, 2009, 11, 3474-3477
1504057 CIFC20 H19 N O4P 1 21/c 16.854; 7.879; 32.765
90; 90; 90		1769.4Xu, Silong; Zhou, Lili; Zeng, San; Ma, Renqin; Wang, Zhihong; He, Zhengjie
Phosphine-mediated olefination between aldehydes and allenes: an efficient synthesis of trisubstituted 1,3-dienes with high E-selectivity.
Organic letters, 2009, 11, 3498-3501
1504058 CIFC16 H17 N O6P -18.2434; 9.3954; 10.116
82.63; 84.66; 80.19		763.6Xu, Silong; Zhou, Lili; Zeng, San; Ma, Renqin; Wang, Zhihong; He, Zhengjie
Phosphine-mediated olefination between aldehydes and allenes: an efficient synthesis of trisubstituted 1,3-dienes with high E-selectivity.
Organic letters, 2009, 11, 3498-3501
1504059 CIFC16 H22 O7P 1 21/c 16.986; 24.324; 18.651
90; 90.932; 90		3168.9Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504060 CIFC16 H22 O7P 1 21/c 110.367; 10.635; 14.676
90; 100.819; 90		1589.3Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504061 CIFC19 H22 O4P 1 21/c 110.489; 13.758; 12.54
90; 123.65; 90		1506.4Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504062 CIFC12 H16 O3P 1 21/c 112.1; 7.3; 12.752
90; 111.89; 90		1045.2Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504063 CIFC21 H26 O6P 1 21/c 17.724; 27.076; 9.347
90; 100.51; 90		1922Aquino, Maurizio; Safir, Imad; Elkhayat, Zobida; Gandara, Zoila; Perez, Manuel; Retailleau, Pascal; Arseniyadis, Siméon
Competing domino processes: path-discriminating ability of epoxide stereochemistry at the angular position.
Organic letters, 2009, 11, 3610-3613
1504064 CIFC25 H26 Br N O4P b c a17.103; 8.857; 29.744
90; 90; 90		4505.7Shintani, Ryo; Hayashi, Shin-ya; Murakami, Masataka; Takeda, Momotaro; Hayashi, Tamio
Stereoselective synthesis of spirooxindoles by palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with isatins.
Organic letters, 2009, 11, 3754-3756
1504065 CIFC16 H19 N O2P 1 21/c 17.1402; 12.5429; 15.2299
90; 101.104; 90		1338.44Li, Cheng; Li, Xinyu; Hong, Ran
Synthetic study on tetrapetalones: stereoselective cyclization of N-acyliminium ion to construct substituted 1-benzazepines.
Organic letters, 2009, 11, 4036-4039
1504066 CIFC16 H17 N O3P 21 21 217.6034; 12.7414; 13.9945
90; 90; 90		1355.76Li, Cheng; Li, Xinyu; Hong, Ran
Synthetic study on tetrapetalones: stereoselective cyclization of N-acyliminium ion to construct substituted 1-benzazepines.
Organic letters, 2009, 11, 4036-4039
1504067 CIFC24 H25 N OP 21 21 216.5177; 15.986; 18.6727
90; 90; 90		1945.55Concellón, José M; Tuya, Paula; del Solar, Virginia; García-Granda, Santiago; Díaz, M Rosario
Efficient and highly selective synthesis of enantiopure cis- or trans-3,4-disubstituted 1,2,3,4-tetrahydroisoquinolines.
Organic letters, 2009, 11, 3750-3753
1504068 CIFC24 H28 O6 S2P 1 21/c 110.3844; 11.1279; 19.5084
90; 98.041; 90		2232.2Tarselli, Michael A.; Zuccarello, J. Lucas; Lee, Stephen J.; Gagné, Michel R
Gold(I)-catalyzed cascade cyclization of allenyl epoxides.
Organic letters, 2009, 11, 3490-3492
1504069 CIFC34 H36 F6 Mn N4 O6 S2P 43 21 215.0588; 15.0588; 15.827
90; 90; 90		3589Wu, Mei; Wang, Bin; Wang, Shoufeng; Xia, Chungu; Sun, Wei
Asymmetric epoxidation of olefins with chiral bioinspired manganese complexes.
Organic letters, 2009, 11, 3622-3625
1504070 CIFC42 H40 F6 Mn N4 O6 S2P 21 21 2117.639; 16.204; 16.203
90; 90; 90		4631.2Wu, Mei; Wang, Bin; Wang, Shoufeng; Xia, Chungu; Sun, Wei
Asymmetric epoxidation of olefins with chiral bioinspired manganese complexes.
Organic letters, 2009, 11, 3622-3625
1504071 CIFC17 H22 Br N3 O5R 3 :H21.619; 21.619; 12.828
90; 90; 120		5192.3Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun
Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles.
Organic letters, 2009, 11, 3874-3877
1504072 CIFC23 H26 Cl N3 O5P -18.9418; 12.02; 12.756
115.51; 92.14; 107.65		1156.4Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun
Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles.
Organic letters, 2009, 11, 3874-3877
1504073 CIFC13 H11 N O SP 1 21 15.8503; 8.4929; 10.957
90; 95.88; 90		541.55Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun
Highly enantioselective and organocatalytic alpha-amination of 2-oxindoles.
Organic letters, 2009, 11, 3874-3877
1504074 CIFC33 H24 OP 21 21 2110.4248; 11.0694; 20.658
90; 90; 90		2383.9Chen, Yifeng; Lu, Yuhua; Li, Guijie; Liu, Yuanhong
Gold-catalyzed cascade Friedel-Crafts/furan-alkyne cycloisomerizations for the highly efficient synthesis of arylated (Z)-enones or -enals.
Organic letters, 2009, 11, 3838-3841
1504075 CIFC16 H18 O2P 1 21/c 19.971; 8.96; 15.88
90; 103.924; 90		1377Zheng, Zhao-Jing; Shu, Xing-Zhong; Ji, Ke-Gong; Zhao, Shu-Chun; Liang, Yong-Min
Acid-catalyzed skeletal rearrangement of epoxy alkynes: a fast access to highly functionalized allenes.
Organic letters, 2009, 11, 3214-3217
1504076 CIFC15 H17 Cl O2P 1 21/c 19.4886; 8.7358; 16.598
90; 95.417; 90		1369.7Zheng, Zhao-Jing; Shu, Xing-Zhong; Ji, Ke-Gong; Zhao, Shu-Chun; Liang, Yong-Min
Acid-catalyzed skeletal rearrangement of epoxy alkynes: a fast access to highly functionalized allenes.
Organic letters, 2009, 11, 3214-3217
1504077 CIFC30 H34 B2 O4F d d 236.848; 45.584; 6.2397
90; 90; 90		10481Kimoto, Takakazu; Tanaka, Kenro; Sakai, Yoshimasa; Ohno, Akira; Yoza, Kenji; Kobayashi, Kenji
2,8- and 2,9-Diboryltetracenes as useful building blocks for extended pi-conjugated tetracenes.
Organic letters, 2009, 11, 3658-3661
1504078 CIFC26.52 H48.95 N8.26 O13.48 SC 1 2/c 121.0704; 8.8723; 20.4017
90; 121.08; 90		3266.5Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504079 CIFC26 H54 N8 O18 P2P -18.1169; 11.2001; 11.4236
108.885; 93.062; 107.523		923.8Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504080 CIFC32 H60 N8 O13 SP 1 21/c 110.753; 20.1934; 17.5334
90; 99.367; 90		3756.4Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504081 CIFC35.32 H62.76 N8 O14.77 PP 1 21/n 110.4079; 20.877; 20.852
90; 102.5; 90		4423.4Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504082 CIFC31 H56 N8 O14 P2P 1 21/c 121.554; 20.961; 17.568
90; 97.789; 90		7864Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504083 CIFC36 H52 N8 O8P b c a14.488; 18.236; 28.915
90; 90; 90		7639Kang, Sung Ok; Day, Victor W.; Bowman-James, Kristin
The influence of amine functionalities on anion binding in polyamide-containing macrocycles.
Organic letters, 2009, 11, 3654-3657
1504084 CIFC17 H24 N2 O4C 1 2 123.342; 5.7712; 17.317
90; 130.887; 90		1763.6Duguet, Nicolas; Slawin, Alexandra M. Z.; Smith, Andrew D.
An asymmetric hetero-claisen approach to 3-alkyl-3-aryloxindoles.
Organic letters, 2009, 11, 3858-3861
1504085 CIFC15 H13 N O3P 1 21/c 111.11; 5.629; 20.2
90; 96.287; 90		1255.7Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504086 CIFC21 H19 N O4 SP -18.351; 9.897; 12.327
110.85; 90.686; 101.286		930Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504087 CIFC13 H15 N O2P 1 21/c 15.735; 15.439; 13.086
90; 110.233; 90		1087.2Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504088 CIFC18 H18 Cl3 N O3P n a 2110.096; 14.429; 13.147
90; 90; 90		1915.2Hermange, Philippe; Tran Huu Dau, Marie Elise; Retailleau, Pascal; Dodd, Robert H.
Highly diastereoselective three-component vinylogous Mannich reaction between isoquinolines, acyl/sulfonyl chlorides, and silyloxyfurans.
Organic letters, 2009, 11, 4044-4047
1504089 CIFC18 H19 N O3P 1 21/n 110.6641; 7.8382; 18.3358
90; 95.948; 90		1524.39Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504090 CIFC24 H20 O2F d d 219.0037; 35.6919; 10.5937
90; 90; 90		7185.5Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504091 CIFC21 H20 OP n a 2121.2315; 6.5111; 10.7839
90; 90; 90		1490.77Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504092 CIFC23 H20 O2P 1 21/n 116.7615; 10.1571; 20.7291
90; 108.722; 90		3342.36Valiulin, Roman A.; Kutateladze, Andrei G.
Harvesting the strain installed by a Paternò-Büchi step in a synthetically useful way: high-yielding photoprotolytic oxametathesis in polycyclic systems.
Organic letters, 2009, 11, 3886-3889
1504093 CIFC60 H86 O8P -112.5; 12.906; 18.607
78.959; 78.684; 70.333		2746Kuno, Lev; Biali, Silvio E.
Restricted rotation of tert-butyl groups in sterically crowded methylene-functionalized calix[4]arenes.
Organic letters, 2009, 11, 3662-3665
1504094 CIFC28 H20 OP -19.6634; 13.954; 15.464
76.183; 88.614; 80.276		1995.5Meyer, S. Todd; Hergenrother, Paul J.
Small molecule ligands for bulged RNA secondary structures.
Organic letters, 2009, 11, 4052-4055
1504095 CIFC28 H20 OP 1 21/c 117.1785; 6.5035; 17.2798
90; 101.927; 90		1888.8Meyer, S. Todd; Hergenrother, Paul J.
Small molecule ligands for bulged RNA secondary structures.
Organic letters, 2009, 11, 4052-4055
1504096 CIFC23 H34 O4C 1 2 126.323; 6.1374; 13.3377
90; 96.461; 90		2141.1Chin, Yen-Jin; Wang, Shun-Yi; Loh, Teck-Peng
Synthesis of iriomoteolide-1a C13-C23 fragment via asymmetric conjugate addition and Julia-Kocienski coupling reaction.
Organic letters, 2009, 11, 3674-3676
1504097 CIFC20 H26 O3P -18.454; 10.416; 11.534
111.416; 94.438; 104.322		900.2Beauseigneur, Alice; Ericsson, Cecilia; Renaud, Philippe; Schenk, Kurt
B-Alkylcatecholborane-mediated tandem radical conjugated addition-aldol cyclization.
Organic letters, 2009, 11, 3778-3781
1504098 CIFC21 H28 O3P -18.5042; 10.5571; 11.489
110.098; 95.633; 104.645		917.6Beauseigneur, Alice; Ericsson, Cecilia; Renaud, Philippe; Schenk, Kurt
B-Alkylcatecholborane-mediated tandem radical conjugated addition-aldol cyclization.
Organic letters, 2009, 11, 3778-3781
1504099 CIFC14 H14 Cl N OP 1 21/n 19.601; 10.575; 12.022
90; 92.744; 90		1219.2Lu, Shen-Ci; Duan, Xiao-Yong; Shi, Zong-Jun; Li, Bing; Ren, Yu-Wei; Zhang, Wei; Zhang, Yong-Hui; Tu, Zhi-Feng
Photoinduced Intramolecular addition of 3-acyl-2-haloindoles to alkenes.
Organic letters, 2009, 11, 3902-3905
1504100 CIFC14 H14 Cl N OP 1 21/c 19.237; 15.927; 7.966
90; 93.364; 90		1169.92Lu, Shen-Ci; Duan, Xiao-Yong; Shi, Zong-Jun; Li, Bing; Ren, Yu-Wei; Zhang, Wei; Zhang, Yong-Hui; Tu, Zhi-Feng
Photoinduced Intramolecular addition of 3-acyl-2-haloindoles to alkenes.
Organic letters, 2009, 11, 3902-3905
1504101 CIFC12 H11 N3 O2P 1 21/n 17.5084; 8.3001; 17.5331
90; 92.508; 90		1091.6Shi, Baolu; Lewis, William; Campbell, Ian B.; Moody, Christopher J.
A concise route to pyridines from hydrazides by metal carbene N-H insertion, 1,2,4-triazine formation, and Diels-Alder reaction.
Organic letters, 2009, 11, 3686-3688
1504102 CIFC26 H20 N2P 21 21 2110.0514; 10.6807; 17.5467
90; 90; 90		1883.74Eisch, John J.; Manchanayakage, Renuka N.; Rheingold, Arnold L.
Attempted generation of the potentially aromatic 6,7-diphenyldibenzo[e,g][1,4]diazocine dianion leads with profound rearrangement to the isomeric n-(2-amino-1,2-diphenylethenyl)carbazole dianions.
Organic letters, 2009, 11, 4060-4063
1504103 CIFC26 H20 N2P -17.3565; 13.3596; 19.9232
92.014; 98.566; 99.128		1908.2Eisch, John J.; Manchanayakage, Renuka N.; Rheingold, Arnold L.
Attempted generation of the potentially aromatic 6,7-diphenyldibenzo[e,g][1,4]diazocine dianion leads with profound rearrangement to the isomeric n-(2-amino-1,2-diphenylethenyl)carbazole dianions.
Organic letters, 2009, 11, 4060-4063
1504104 CIFC27 H24 N2 O3P b c n33.2133; 7.9061; 17.9377
90; 90; 90		4710.2Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504105 CIFC25 H26 N2 O3P -19.0795; 11.1502; 11.7893
65.448; 88.094; 78.917		1063.91Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504106 CIFC27 H26 N2 O3P 1 21/n 110.824; 14.282; 16.681
90; 101.355; 90		2528.2Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504107 CIFC25 H28 N2 O3P b c a13.0902; 16.4023; 19.4869
90; 90; 90		4184Lin, Chi-Hui; Jhang, Jing-Fu; Yang, Ding-Yah
One-pot synthesis of coumarin-based oxazabicyclic and oxazatricyclic compounds and their fluorescence redox switching properties.
Organic letters, 2009, 11, 4064-4067
1504108 CIFC30 H48 N2 O13P 21 21 219.3504; 18.666; 20.153
90; 90; 90		3517.4Gao, Zheng-Xi; Wang, Meng; Wang, Shaozhong; Yao, Zhu-Jun
Efficient synthesis of 4-amido-N(5)-acetyl-4-deoxyneuraminic acid and its application to the C-4 modification of sialic acids.
Organic letters, 2009, 11, 3678-3681
1504109 CIFC18 H2 Br N4 O2P 1 21/c 17.816; 19.39; 12.728
90; 91.5; 90		1928.3Semakin, Artem N.; Sukhorukov, Alexey Yu; Lesiv, Alexey V.; Ioffe, Sema L.; Lyssenko, Konstantin A.; Nelyubina, Yulia V.; Tartakovsky, Vladimir A.
Unusual intramolecular cyclization of tris(beta-oximinoalkyl)amines. the first synthesis of 1,4,6,10-tetraazaadamantanes.
Organic letters, 2009, 11, 4072-4075
1504110 CIFC22 H50 N8 O16P 1 21 18.0368; 16.0616; 11.7596
90; 100.562; 90		1492.26Semakin, Artem N.; Sukhorukov, Alexey Yu; Lesiv, Alexey V.; Ioffe, Sema L.; Lyssenko, Konstantin A.; Nelyubina, Yulia V.; Tartakovsky, Vladimir A.
Unusual intramolecular cyclization of tris(beta-oximinoalkyl)amines. the first synthesis of 1,4,6,10-tetraazaadamantanes.
Organic letters, 2009, 11, 4072-4075
1504111 CIFC22 H20 SiP -19.318; 9.838; 10.808
77.76; 68.27; 70.39		862.6Ilies, Laurean; Tsuji, Hayato; Nakamura, Eiichi
Synthesis of benzo[b]siloles via KH-promoted cyclization of (2-alkynylphenyl)silanes.
Organic letters, 2009, 11, 3966-3968
1504112 CIFC73 H105.74 F24 N40 Na3.33 O56.53C 1 2/c 151.867; 16.796; 36.2025
90; 124.185; 90		26089.2Huang, Wei-Hao; Zavalij, Peter Y.; Isaacs, Lyle
Metal-ion-induced folding and dimerization of a glycoluril decamer in water.
Organic letters, 2009, 11, 3918-3921
1504113 CIFC120 H174.15 F9 N80 Na7 O81.07 S2P -123.465; 30.5747; 31.8174
108.231; 99.079; 110.589		19353.8Huang, Wei-Hao; Zavalij, Peter Y.; Isaacs, Lyle
Metal-ion-induced folding and dimerization of a glycoluril decamer in water.
Organic letters, 2009, 11, 3918-3921
1504114 CIFC24 H18 Cl2 O2P 1 21 16.797; 27.1487; 10.6266
90; 100.197; 90		1929.95Oswald, Claire L.; Peterson, Justine A.; Lam, Hon Wai
Enantioselective copper-catalyzed reductive Michael cyclizations.
Organic letters, 2009, 11, 4504-4507
1504115 CIFC29 H29 Cl2 N O5P 1 21/c 16.1649; 8.0908; 51.2892
90; 92.662; 90		2555.49Oswald, Claire L.; Peterson, Justine A.; Lam, Hon Wai
Enantioselective copper-catalyzed reductive Michael cyclizations.
Organic letters, 2009, 11, 4504-4507
1504116 CIFC14 H13 N O4 SP 1 21/n 19.2571; 13.4283; 11.0755
90; 94.92; 90		1371.69Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K.
Acyl-isothiocyanates as efficient thiocyanate transfer reagents.
Organic letters, 2009, 11, 3382-3385
1504117 CIFC20 H16 N2 O4 S2C 1 2/c 132.3486; 7.7362; 18.9463
90; 124.921; 90		3887.7Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K.
Acyl-isothiocyanates as efficient thiocyanate transfer reagents.
Organic letters, 2009, 11, 3382-3385
1504118 CIFC10 H9 N O2 SP b c a9.4658; 10.2821; 19.9354
90; 90; 90		1940.28Palsuledesai, Charuta C.; Murru, Siva; Sahoo, Santosh K.; Patel, Bhisma K.
Acyl-isothiocyanates as efficient thiocyanate transfer reagents.
Organic letters, 2009, 11, 3382-3385
1504119 CIFC17 H15 I N2 O2P 1 21/n 17.8625; 10.7999; 18.3965
90; 90.968; 90		1561.9Kramer, Søren; Dooleweerdt, Karin; Lindhardt, Anders Thyboe; Rottländer, Mario; Skrydstrup, Troels
Highly regioselective Au(I)-catalyzed hydroamination of ynamides and propiolic acid derivatives with anilines.
Organic letters, 2009, 11, 4208-4211
1504120 CIFC27 H23 N O4 SP 1 21 112.7746; 5.8697; 16.037
90; 102.412; 90		1174.4Lu, Hai-Hua; Zhang, Fu-Gen; Meng, Xiang-Gao; Duan, Shu-Wen; Xiao, Wen-Jing
Enantioselective Michael reactions of beta, beta-disubstituted nitroalkenes: a new approach to beta(2,2)-amino acids with hetero-quaternary stereocenters.
Organic letters, 2009, 11, 3946-3949
1504121 CIFC23 H23 Br N O4 SP 1 21/c 110.96; 16.77; 12.38
90; 100.46; 90		2237.6Wei, 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
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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