Crystallography Open Database

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1519698 CIFC10 H13 F OP 21 21 215.5342; 11.1421; 14.6505
90; 90; 90
903.39Witten, Michael R.; Jacobsen, Eric N.
A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes.
Organic letters, 2015, 17, 2772-2775
1519755 CIFC15 H16 O4P 1 21/c 17.4665; 21.583; 8.4033
90; 107.586; 90
1290.9Zhang, Xuxue; Dai, Wenpeng; Wu, Wei; Cao, Song
Copper-Catalyzed Coupling Cyclization of gem-Difluoroalkenes with Activated Methylene Carbonyl Compounds: Facile Domino Access to Polysubstituted Furans.
Organic letters, 2015, 17, 2708-2711
1519756 CIFC30 H42 O5P 1 21 17.3312; 12.6193; 14.4778
90; 98.847; 90
1323.47Zhao, Qian-Qian; Song, Qiu-Yan; Jiang, Kan; Li, Guang-Da; Wei, Wen-Jun; Li, Ya; Gao, Kun
Spirochensilides A and B, Two New Rearranged Triterpenoids from Abies chensiensis.
Organic letters, 2015, 17, 2760-2763
1519757 CIFC10 H7 Br Cl2 N2 OP b c a12.6226; 12.3709; 14.1124
90; 90; 90
2203.7Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519758 CIFC12 H12 Br2 N2 OP 1 21/c 17.3945; 20.124; 17.43
90; 91.44; 90
2592.9Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519759 CIFC11 H10 Br2 N2P 1 21/c 114.9133; 10.5056; 7.3297
90; 103.561; 90
1116.35Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519760 CIFC11 H7 Cl2 F3 N2 O1.5P 1 21/c 17.501; 40.025; 16.7795
90; 94.664; 90
5021Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519761 CIFC11 H9 Br2 F N2P b c a14.443; 7.5861; 21.306
90; 90; 90
2334.4Gurry, Michael; Sweeney, Martin; McArdle, Patrick; Aldabbagh, Fawaz
One-pot hydrogen peroxide and hydrohalic Acid induced ring closure and selective aromatic halogenation to give new ring-fused benzimidazoles.
Organic letters, 2015, 17, 2856-2859
1519848 CIFC12 H14 O3P 1 21/c 18.8887; 18.4179; 6.9957
90; 115.638; 90
1032.52Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519849 CIFC12 H14 O3P 1 21/c 110.7308; 8.7467; 12.089
90; 109.485; 90
1069.68Hassan, Ahmed H. E.; Lee, Jae Kyun; Pae, Ae Nim; Min, Sun-Joon; Cho, Yong Seo
Synthesis of the Tricyclic Ring Structure of Daphnanes via Intramolecular [4 + 3] Cycloaddition/SmI2-Pinacol Coupling.
Organic letters, 2015, 17, 2672-2675
1519850 CIFC22 H16 Br N O2P 1 21/c 15.7399; 15.532; 20.365
90; 96.93; 90
1802.3Dhanasekaran, Sivasankaran; Kayet, Anirban; Suneja, Arun; Bisai, Vishnumaya; Singh, Vinod K.
Unified Approach to Isoindolinones and THIQs via Lewis Acid Catalyzed Domino Mukaiyama-Mannich Lactamization/Alkylations: Application in the Synthesis of (±)-Homolaudanosine.
Organic letters, 2015, 17, 2780-2783
1519851 CIFC16 H12 N4P 1 21/c 14.8624; 11.167; 23.437
90; 94.33; 90
1269Jia, Feng-Cheng; Xu, Cheng; Zhou, Zhi-Wen; Cai, Qun; Li, Deng-Kui; Wu, An-Xin
Consecutive Cycloaddition/SNAr/Reduction/Cyclization/Oxidation Sequences: A Copper-Catalyzed Multicomponent Synthesis of Fused N-Heterocycles.
Organic letters, 2015, 17, 2820-2823
1519923 CIFC21 H34 O3P 1 21 16.1791; 23.0423; 6.9392
90; 110.037; 90
928.21Hosseini, Abolfazl; Seidel, Daniel; Miska, Andreas; Schreiner, Peter R.
Fluoride-assisted activation of calcium carbide: a simple method for the ethynylation of aldehydes and ketones.
Organic letters, 2015, 17, 2808-2811
1519924 CIFC25 H21 Fe N3P 1 21/c 110.9392; 8.3314; 22.5089
90; 102.759; 90
2000.78Wei, Fang; Li, Haoyu; Song, Chuanling; Ma, Yudao; Zhou, Ling; Tung, Chen-Ho; Xu, Zhenghu
Cu/Pd-Catalyzed, Three-Component Click Reaction of Azide, Alkyne, and Aryl Halide: One-Pot Strategy toward Trisubstituted Triazoles.
Organic letters, 2015, 17, 2860-2863
1519998 CIFC20 H30 N0 O5P 21 21 217.0685; 15.143; 17.388
90; 90; 90
1861.2Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1519999 CIFC20 H28 O5P 1 21 19.4777; 7.3392; 13.4089
90; 91.432; 90
932.41Annam, S Ch V Appa Rao; Ankireddy, Madhu; Sura, Madhu Babu; Ponnapalli, Mangala Gowri; Sarma, Akella V. S.; S, Jeelani Basha
Epimeric Excolides from the Stems of Excoecaria agallocha and Structural Revision of Rhizophorin A.
Organic letters, 2015, 17, 2840-2843
1520000 CIFC29 H36 O8P 1 21/c 113.2416; 13.1779; 15.2428
90; 109.387; 90
2509Fukaya, Keisuke; Kodama, Keisuke; Tanaka, Yuta; Yamazaki, Hirohisa; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis.
Organic letters, 2015, 17, 2574-2577
1520001 CIFC54 H46 Co N2 P3P 1 21/n 114.376; 14.699; 21.34
90; 107.79; 90
4293.8Scheuermann, Margaret L.; Johnson, Elizabeth J.; Chirik, Paul J.
Alkene isomerization-hydroboration promoted by phosphine-ligated cobalt catalysts.
Organic letters, 2015, 17, 2716-2719
1520002 CIFC29 H38 O8P 1 21/n 19.3612; 19.6336; 14.1965
90; 101.762; 90
2554.4Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520003 CIF
Paper
C42 H50 O10P -19.6397; 13.6008; 15.0461
83.6966; 77.488; 77.9768
1879.2Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520004 CIFC30.25 H41 O8P -111.3343; 15.4666; 16.487
85.1124; 78.3773; 78.5231
2771.3Fukaya, Keisuke; Tanaka, Yuta; Sato, Ayako C.; Kodama, Keisuke; Yamazaki, Hirohisa; Ishimoto, Takeru; Nozaki, Yasuyoshi; Iwaki, Yuki M.; Yuki, Yohei; Umei, Kentaro; Sugai, Tomoya; Yamaguchi, Yu; Watanabe, Ami; Oishi, Takeshi; Sato, Takaaki; Chida, Noritaka
Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization.
Organic letters, 2015, 17, 2570-2573
1520005 CIFC15 H21 N O2P 1 21/c 18.5353; 10.6984; 15.609
90; 104.429; 90
1380.4Zhou, Wei; Ni, Shengyang; Mei, Haibo; Han, Jianlin; Pan, Yi
Hydroxyalkylation-initiated radical cyclization of N-allylbenzamide for direct construction of isoquinolinone.
Organic letters, 2015, 17, 2724-2727
1520068 CIFC32 H36 Br2 N4 O2P 1 21/c 110.037; 8.2451; 18.991
90; 101.279; 90
1541.3Zhu, Xiaxia; Du, Haifeng
A Highly Stereoselective Metal-Free Hydrogenation of Diimines for the Synthesis of Cis-Vicinal Diamines.
Organic letters, 2015, 17, 3106-3109
1520116 CIFC28 H19 NP -19.0455; 9.563; 11.529
103.716; 98.763; 98.986
938.1Liu, Xingyan; Li, Xiaoyu; Liu, Hu; Guo, Qiang; Lan, Jingbo; Wang, Ruilin; You, Jingsong
Aldehyde as a Traceless Directing Group for Rh(III)-Catalyzed C-H Activation: A Facile Access to Diverse Indolo[1,2-a]quinolines.
Organic letters, 2015, 17, 2936-2939
1520117 CIFC17.5 H18 F8 I O3.5 S2P -18.9435; 12.1892; 12.2642
63.163; 87.526; 77.6
1162.92Matsuzaki, Kohei; Okuyama, Kenta; Tokunaga, Etsuko; Saito, Norimichi; Shiro, Motoo; Shibata, Norio
Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles.
Organic letters, 2015, 17, 3038-3041
1520220 CIFC24 H19 NC 1 2/c 142.784; 6.0454; 31.552
90; 119.951; 90
7071Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520221 CIFC30 H23 NP 1 21/c 112.0216; 6.2012; 30.083
90; 101.315; 90
2199Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520222 CIFC23 H19 NC 1 2/c 129.558; 6.041; 19.696
90; 104.661; 90
3402.4Li, Xiangdong; Chen, Ming; Xie, Xin; Sun, Ning; Li, Shi; Liu, Yuanhong
Synthesis of Multiple-Substituted Pyrroles via Gold(I)-Catalyzed Hydroamination/Cyclization Cascade.
Organic letters, 2015, 17, 2984-2987
1520223 CIFC14 H16 Cl3 N O3P 3216.1172; 16.1172; 5.6393
90; 90; 120
1268.63Skvorcova, Marija; Grigorjeva, Liene; Jirgensons, Aigars
Tetrahydro-1,3-oxazepines via Intramolecular Amination of Cyclopropylmethyl Cation.
Organic letters, 2015, 17, 2902-2904
1520224 CIFC22 H22 N4 O2 SP 1 21 110.363; 9.318; 11.453
90; 112.7; 90
1020.3Wang, Linqing; Yang, Dongxu; Li, Dan; Wang, Rui
Catalytic Enantioselective Ring-Opening and Ring-Closing Reactions of 3-Isothiocyanato Oxindoles and N-(2-Picolinoyl)aziridines.
Organic letters, 2015, 17, 3004-3007
1520225 CIFC13 H21 N3 O3P 1 21/c 14.5905; 23.474; 13.2529
90; 91.746; 90
1427.4Martínez, Luís; Martorell, Gabriel; Sampedro, Ángel; Ballester, Pablo; Costa, Antoni; Rotger, Carmen
Hydrogen Bonded Squaramide-Based Foldable Module Induces Both β- and α-Turns in Hairpin Structures of α-Peptides in Water.
Organic letters, 2015, 17, 2980-2983
1520297 CIFC52 H60 Br N4 O18 S2C 1 2/c 126.6011; 19.037; 14.4208
90; 114.731; 90
6633Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520298 CIFC52 H86 N4 O32 S2P 1 21/n 111.8381; 23.4128; 11.8991
90; 107.339; 90
3148.12Carrasco-Ruiz, Anayeli; Tiburcio, Jorge
Electrostatic Kinetic Barriers in the Threading/Dethreading Motion of a Rotaxane-like Complex.
Organic letters, 2015, 17, 1858-1861
1520299 CIFC22 H23 I O3P 21 21 215.7232; 10.8546; 32.913
90; 90; 90
2044.7Merad, Jérémy; Borkar, Prashant; Bouyon Yenda, Tracy; Roux, Christèle; Pons, Jean-Marc; Parrain, Jean-Luc; Chuzel, Olivier; Bressy, Cyril
Highly Enantioselective Acylation of Acyclic Meso 1,3-Diols through Synergistic Isothiourea-Catalyzed Desymmetrization/Chiroablative Kinetic Resolution.
Organic letters, 2015, 17, 2118-2121
1520300 CIFC36 H46 N4 O2P -17.1052; 14.1156; 16.3735
105.153; 91.858; 102.309
1541.85Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520301 CIFC41 H58.333 N5 OP 1 21/c 126.0651; 15.2582; 9.5468
90; 96.584; 90
3771.8Meehan, Eileen; Li, Ruoshi; Zeller, Matthias; Brückner, Christian
Octaethyl-1,3-oxazinochlorin: A β-Octaethylchlorin Analogue Made by Pyrrole Expansion.
Organic letters, 2015, 17, 2210-2213
1520302 CIFC33 H31 Br2 N O6P 1 21/c 118.4779; 9.1189; 19.3437
90; 109.352; 90
3075.2Tang, Shaojian; Park, Jong Yeun; Yeagley, Andrew A.; Sabat, Michal; Chruma, Jason J.
Decarboxylative Generation of 2-Azaallyl Anions: 2-Iminoalcohols via a Decarboxylative Erlenmeyer Reaction.
Organic letters, 2015, 17, 2042-2045
1520303 CIFC13 H23 Cl N2 NiP 1 21/n 111.1164; 12.6843; 11.5897
90; 118.363; 90
1438.02Shields, Jason D.; Gray, Erin E.; Doyle, Abigail G.
A modular, air-stable nickel precatalyst.
Organic letters, 2015, 17, 2166-2169
1520304 CIFC66.33 H81.67 N2 O4 YbP 21 21 2115.592; 20.5827; 60.065
90; 90; 90
19276.4Zeng, Chao; Yuan, Dan; Zhao, Bei; Yao, Yingming
Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Catalyzed by Rare-Earth Amides [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 with Phenoxy-Functionalized Chiral Prolinols.
Organic letters, 2015, 17, 2242-2245
1520305 CIFC6 H9 N O4C 1 2/c 116.4651; 6.6186; 14.9686
90; 109.033; 90
1542Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520306 CIFC12 H19 N O3P 1 21/c 111.0623; 9.4884; 11.6015
90; 90.961; 90
1217.56Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520307 CIFC10 H16 B F2 N O3P -19.5474; 11.4938; 11.5223
92.227; 96.964; 91.605
1253.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520308 CIFC12 H20 B F2 N O3P 1 21/n 17.8638; 14.0418; 12.6427
90; 91.6599; 90
1395.45Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520309 CIFC12 H18 B F2 N O3P 1 21 114.7772; 11.1085; 16.6848
90; 92.405; 90
2736.4Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520310 CIFC13 H20 B F2 N O3P 1 21/n 110.6399; 11.8723; 11.9174
90; 107.028; 90
1439.41Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520311 CIFC12 H18 B F2 N O4P -111.3963; 11.7254; 12.5468
74.986; 64.116; 64.237
1353.47Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520312 CIFC10 H16 B F2 N O4I b a 212.1721; 49.556; 8.341
90; 90; 90
5031.3Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520313 CIFC10 H16 B F2 N O4P -17.0022; 7.7079; 12.3657
83.232; 83.476; 76.265
641.26Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520314 CIFC10 H17 N O4P -17.8792; 8.1476; 10.2749
106.191; 106.585; 104.538
566.58Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520315 CIFC12 H20 B F2 N O4P b c a16.8311; 9.1985; 18.0999
90; 90; 90
2802.24Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520316 CIFC12 H18 B Br2 F2 N O4P 1 21/c 110.3517; 15.7916; 9.5485
90; 99.476; 90
1539.59Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520317 CIFC8 H11 Br O4P 1 21/c 18.8688; 18.0772; 6.0396
90; 94.753; 90
964.96Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520318 CIFC19 H23.6 B F2 N2 O5.3P b c n12.2584; 10.1061; 31.0115
90; 90; 90
3841.8Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520319 CIFC19 H23 B F2 N2 O5P 1 21/n 115.4609; 8.0727; 15.6576
90; 103.611; 90
1899.36Roßbach, Jan; Harms, Klaus; Koert, Ulrich
α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements.
Organic letters, 2015, 17, 3122-3125
1520320 CIFC30 H25 N2 O4 PP 1 21/c 112.5638; 14.8917; 13.7164
90; 104.477; 90
2484.8Yamamura, Masaki; Takizawa, Hiroyuki; Nabeshima, Tatsuya
Zwitterionic N2O2-Type Protonated Dipyrrin Bearing a Phosphate Anionic Moiety as a pH-Responsive Fluorescence Indicator.
Organic letters, 2015, 17, 3114-3117
1520385 CIFC41 H45 Cl2 N5 O18P -118.718; 20.1801; 21.555
63.466; 65.8; 82.646
6629.1Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520386 CIFC48 H53 N5 O16 S2P 1 21/n 19.5948; 11.7166; 43.6295
90; 91.392; 90
4903.3Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520387 CIFC48 H51 N5 O13 SP 1 21/c 110.656; 38.925; 11.435
90; 111.21; 90
4422Rana, Anup; Sathish Kumar, B.; Panda, Pradeepta K.
β-Decamethoxysapphyrin and Its N-Benzyl Analogue.
Organic letters, 2015, 17, 3030-3033
1520388 CIFC22 H19 N O2P 21 21 218.6008; 10.6881; 18.1
90; 90; 90
1663.9Battini, Narsaiah; Battula, Satyanarayana; Kumar, Raju Ranjith; Ahmed, Qazi Naveed
2-Oxo Driven Unconventional reactions: Microwave Assisted Approaches to Tetrahydrofuro[3,2-d]oxazoles and Furanones.
Organic letters, 2015, 17, 2992-2995
1520439 CIFC26 H18 B Cl2 F8 N3P 1 21/c 17.923; 11.039; 27.77
90; 96.981; 90
2410.8Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520440 CIFC26.14 H22.79 B Cl0.79 F2 N3 O3.24P 1 21/c 113.159; 12.065; 15.082
90; 98.075; 90
2370.7Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520441 CIFC707 H656 B16 F32 N48 O9P 1 21/c 115.429; 41.602; 24.49
90; 91.209; 90
15716Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520442 CIFC35.79 H27.57 B Cl1.57 F2 N3C 1 2/c 133.021; 10.588; 23.034
90; 132.89; 90
5900Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520443 CIFC32 H24 B Cl2 F2 N3P -17.3425; 11.0127; 15.884
94.772; 97.467; 91.375
1268.3Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520444 CIFC50.45 H44.9 B Cl2.9 F2 N3P 1 21/c 18.0911; 21.853; 25.007
90; 97.291; 90
4385.9Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520445 CIFC23 H18 B F2 N3P 1 21/n 19.594; 8.7428; 21.526
90; 100.795; 90
1773.6Maeda, Chihiro; Todaka, Takumi; Ema, Tadashi
Carbazole-Based Boron Dipyrromethenes (BODIPYs): Facile Synthesis, Structures, and Fine-Tunable Optical Properties.
Organic letters, 2015, 17, 3090-3093
1520446 CIFC16 H15 N O2 S2P c a 2118.773; 7.8448; 20.3148
90; 90; 90
2991.8Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520447 CIFC16 H14 F N O2 S2P 1 21/c 115.7817; 13.0488; 7.2719
90; 92.391; 90
1496.2Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520448 CIFC16 H15 N O3 S2P -19.7686; 10.4236; 16.0412
90.974; 91.846; 107.681
1554.8Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520449 CIFC16 H15 N O2 S SeP b c a7.38023; 12.875; 31.8273
90; 90; 90
3024.24Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520450 CIFC17 H17 N O2 S2P 1 21/n 16.63588; 12.9255; 19.0476
90; 93.665; 90
1630.41Siva Reddy, Alla; Kumara Swamy, K. C.
Use of Elemental Sulfur or Selenium in a Novel One-Pot Copper-Catalyzed Tandem Cyclization of Functionalized Ynamides Leading to Benzosultams.
Organic letters, 2015, 17, 2996-2999
1520451 CIFC40 H32 N2P 1 21/n 112.149; 7.34; 16.53
90; 101.456; 90
1444.7Xu, Feng; Peng, Lifen; Shinohara, Kenta; Nishida, Takanori; Wakamatsu, Kan; Uejima, Motoyuki; Sato, Tohru; Tanaka, Kazuyoshi; Machida, Norihiko; Akashi, Haruo; Orita, Akihiro; Otera, Junzo
One-Shot Double Amination of Sondheimer-Wong Diynes: Synthesis of Photoluminescent Dinaphthopentalenes.
Organic letters, 2015, 17, 3014-3017
1520491 CIFC60 H74 N4 O4P -111.2497; 12.373; 20.0241
95.185; 106.067; 94.622
2651.1Xia, Debin; Marszalek, Tomasz; Li, Mengmeng; Guo, Xin; Baumgarten, Martin; Pisula, Wojciech; Müllen, Klaus
Solution-Processable n-Type Organic Semiconductors Based on Angular-Shaped 2-(12H-Dibenzofluoren-12-ylidene)malononitrilediimide.
Organic letters, 2015, 17, 3074-3077
1520504 CIFC20 H16 I N OP -110.699; 11.726; 22.2683
94.284; 101.795; 109.369
2549Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520505 CIFC20 H16 I N OP b c a7.2355; 20.9295; 23.0167
90; 90; 90
3485.5Wang, Jia; Zhu, Hai-Tao; Qiu, Yi-Feng; Niu, Yuan; Chen, Si; Li, Ying-Xiu; Liu, Xue-Yuan; Liang, Yong-Min
Facile Synthesis of Carbazoles via a Tandem Iodocyclization with 1,2-Alkyl Migration and Aromatization.
Organic letters, 2015, 17, 3186-3189
1520513 CIFC24 H24P 1 21/n 17.4014; 30.606; 7.739
90; 100.806; 90
1722Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520514 CIFC20 H24 O4 SP 1 n 111.2988; 5.7063; 14.045
90; 102.129; 90
885.3Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520515 CIFC25 H29 N O5 SF d d 222.419; 52.094; 7.523
90; 90; 90
8786Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520516 CIFC25 H29 N O5 SC 1 2/c 130.166; 11.6914; 14.2065
90; 113.297; 90
4601.9Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520517 CIFC19 H19 F OP 21 21 218.4903; 9.6656; 18.663
90; 90; 90
1531.6Chang, Meng-Yang; Cheng, Yu-Chieh; Lu, Yi-Ju
Synthesis of Substituted Benzenes via Bi(OTf)3-Mediated Intramolecular Carbonyl Allylation of α-Prenyl or α-Geranyl β-Arylketosulfones.
Organic letters, 2015, 17, 3142-3145
1520518 CIFC43 H41 N3 O4P 1 21/c 131.617; 15.428; 14.478
90; 101.899; 90
6910Zhang, Feng-Lian; Zhu, Xu; Chiba, Shunsuke
Tf~2~NH-Catalyzed Amide Synthesis from Vinyl Azides and Alcohols
Organic Letters, 2015, 17, 3138-3141
1520519 CIFC13 H12 Cl N O4P 21 21 217.9023; 12.49; 12.9
90; 90; 90
1273.2Sekikawa, Tohru; Kitaguchi, Takayuki; Kitaura, Hayato; Minami, Tatsuya; Hatanaka, Yasuo
Catalytic Activity of epi-Quinine-Derived 3,5-Bis(trifluoromethyl)benzamide in Asymmetric Nitro-Michael Reaction of Furanones.
Organic letters, 2015, 17, 3026-3029
1520520 CIFC39 H40 B F2 N3 O4P -18.745; 10.225; 20.19
89.48; 86.38; 65.669
1641.4Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520521 CIFC37.5 H36.5 B Cl1.5 F2 N3 O4P -18.776; 10.567; 19.225
84.193; 82.204; 69.585
1652.6Hiruta, Yuki; Koiso, Hikaru; Ozawa, Hitoshi; Sato, Hiroyasu; Hamada, Kensaku; Yabushita, Satoshi; Citterio, Daniel; Suzuki, Koji
Near IR Emitting Red-Shifting Ratiometric Fluorophores Based on Borondipyrromethene.
Organic letters, 2015, 17, 3022-3025
1520522 CIFC46 H44 B2 N2 O2P 1 21/c 17.274; 17.864; 15.322
90; 100.332; 90
1958.7Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520523 CIFC42 H36 B2 N2 O2P 1 21/c 17.054; 17.672; 13.751
90; 96.406; 90
1703.5Kubota, Yasuhiro; Niwa, Takahiro; Jin, Jiye; Funabiki, Kazumasa; Matsui, Masaki
Synthesis, Absorption, and Electrochemical Properties of Quinoid-Type Bisboron Complexes with Highly Symmetrical Structures.
Organic letters, 2015, 17, 3174-3177
1520542 CIFC32 H25 N O4P 1 21 16.62144; 20.1343; 9.362
90; 100.915; 90
1225.54Zhao, Shuai; Zhao, Yuan-Yuan; Lin, Jun-Bing; Xie, Ting; Liang, Yong-Min; Xu, Peng-Fei
Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives.
Organic letters, 2015, 17, 3206-3209
1520547 CIFC25 H24 SP -19.4128; 9.6074; 12.0794
97.999; 97.992; 108.357
1007.08Zhang, Hang; Wang, Bo; Yi, Heng; Zhang, Yan; Wang, Jianbo
Rh(II)-Catalyzed [2,3]-Sigmatropic Rearrangement of Sulfur Ylides Derived from Cyclopropenes and Sulfides.
Organic letters, 2015, 17, 3322-3325
1520552 CIFC36 H22 N12P 1 21/n 115.3809; 11.5149; 17.7975
90; 90.677; 90
3151.9Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520553 CIFC35 H19 F4 N6 O2 PI b a 221.689; 29.869; 10.7143
90; 90; 90
6941Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520554 CIFC51 H33 Co F4 N8P 1 21/c 112.3996; 15.4999; 21.5037
90; 97.248; 90
4099.8Saltsman, Irena; Goldberg, Israel; Gross, Zeev
Porphyrins and Corroles with 2,6-Pyrimidyl Substituents.
Organic letters, 2015, 17, 3214-3217
1520555 CIFC24 H20 Br2 N2C 1 2/c 116.3504; 14.9527; 9.2389
90; 92.387; 90
2256.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520556 CIFC24 H18 N2P -19.4274; 12.3411; 15.5934
83.302; 82.714; 79.24
1759.9Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520557 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.33; 10.8862; 17.8919
90; 110.048; 90
2622Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520558 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.3809; 10.9748; 11.0438
109.43; 98.185; 97.328
1153.7Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520559 CIFC50 H36 Ag2 F6 N4 O6 S2P -110.4495; 11.0503; 11.0576
109.671; 96.586; 97.962
1172.8Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520560 CIFC62 H50 Ag2 N4 O6 S2P 1 21/c 114.369; 10.925; 18.106
90; 110.574; 90
2661Laird, Rebecca C.; Sinnwell, Michael A.; Nguyen, Nam P.; Swenson, Dale C.; Mariappan, S. V. Santhana; MacGillivray, Leonard R.
Intramolecular [2 + 2] Photodimerization Achieved in the Solid State via Coordination-Driven Self-Assembly.
Organic letters, 2015, 17, 3233-3235
1520561 CIFC51 H58 F6 O14 S2P -111.2709; 11.7647; 20.1194
88.271; 83.035; 86.352
2642.1Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520562 CIFC46 H46 Cl2 F6 O14 S2P 1 n 111.616; 18.2419; 11.617
90; 94.1589; 90
2455.14Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520563 CIFC48.75 H55.04 Cl2.25 F3 O12 SP n a 2135.9931; 12.0648; 11.369
90; 90; 90
4937Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520564 CIFC51 H58 F6 O14 S2P 21 21 2111.3045; 12.1357; 37.187
90; 90; 90
5101.6Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520565 CIFC51 H55 F9 O16 S3P 1 21/c 122.0373; 11.9982; 22.7155
90; 110.288; 90
5633.5Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520566 CIFC51 H55 F9 O16 S3P b c a20.6289; 22.2856; 24.1696
90; 90; 90
11111.4Han, Jie; Hou, Xisen; Ke, Chenfeng; Zhang, Huacheng; Strutt, Nathan L.; Stern, Charlotte L.; Stoddart, J. Fraser
Activation-Enabled Syntheses of Functionalized Pillar[5]arene Derivatives.
Organic letters, 2015, 17, 3260-3263
1520573 CIFC17 H15 N SP 21 21 216.1669; 12.182; 17.8605
90; 90; 90
1341.77Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520574 CIFC19 H17 N OP b c a7.4565; 18.3137; 20.6855
90; 90; 90
2824.73Hardegger, Leo A.; Habegger, Jacqueline; Donohoe, Timothy J.
Modular Synthesis of Highly Substituted Pyridines via Enolate α-Alkenylation.
Organic letters, 2015, 17, 3222-3225
1520575 CIFC16 H15 N3P 1 21/m 19.7773; 6.90436; 9.79548
90; 98.985; 90
653.14Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520576 CIFC21 H15 N3P 1 21/c 114.0946; 11.4421; 9.74761
90; 99.2056; 90
1551.77Castillo, Juan-Carlos; Quiroga, Jairo; Abonia, Rodrigo; Rodriguez, Jean; Coquerel, Yoann
The Aryne aza-Diels-Alder Reaction: Flexible Syntheses of Isoquinolines.
Organic letters, 2015, 17, 3374-3377
1520577 CIFC20 H20 O6P 21 21 2110.1756; 12.2477; 13.4918
90; 90; 90
1681.45Bautista, Elihú; Fragoso-Serrano, Mabel; Toscano, Rubén A; García-Peña, María Del Rosario; Ortega, Alfredo
Teotihuacanin, a Diterpene with an Unusual Spiro-10/6 System from Salvia amarissima with Potent Modulatory Activity of Multidrug Resistance in Cancer Cells.
Organic letters, 2015, 17, 3280-3282
1520614 CIFC25 H23 N O3P 1 21/c 19.4141; 23.293; 9.0609
90; 92.942; 90
1984.3Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520615 CIFC18 H17 N O2P 1 21/c 18.0166; 15.8594; 11.2674
90; 98.788; 90
1415.7Brady, Patrick B.; Carreira, Erick M.
Addition of Trifluoroborates to Oxetanyl N,O-Acetals: Entry into Spiro and Fused Saturated Heterocycles.
Organic letters, 2015, 17, 3350-3353
1520616 CIFC37 H31 N O5P 1 21/n 111.364; 10.93; 24.447
90; 96.564; 90
3017Mo, Lei; Wu, Lin-Lin; Wang, Shaozhong; Yao, Zhu-Jun
Efficient Synthesis of Octahydrophenanthrene Derivatives with Mild Cascade Reactions of Isochromenylium Tetrafluoroborates and Bifunctional Styrenes.
Organic letters, 2015, 17, 3314-3317
1520633 CIFC22 H21 Br N2 O3 S2P b c a11.7745; 15.3391; 24.3582
90; 90; 90
4399.34Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520634 CIFC22 H20 N2 O4 S2P -19.0038; 10.66; 11.8108
75.2664; 76.0323; 75.5364
1042.26Choi, Wonseok; Kim, Jaeeun; Ryu, Taekyu; Kim, Ki-Bbeum; Lee, Phil Ho
Synthesis of N-Imidoyl and N-Oxoimidoyl Sulfoximines from 1-Alkynes, N-Sulfonyl Azides, and Sulfoximines.
Organic letters, 2015, 17, 3330-3333
1520635 CIFC30 H29 N O3P 21 21 217.37176; 14.7771; 21.8173
90; 90; 90
2376.63Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520636 CIFC29 H32 N2 S2P 1 21 110.39896; 9.11807; 13.7409
90; 108.291; 90
1237.06Majumdar, Nilanjana; Saito, Akira; Yin, Liang; Kumagai, Naoya; Shibasaki, Masakatsu
Direct Catalytic Asymmetric Conjugate Addition of Saturated and Unsaturated Thioamides.
Organic letters, 2015, 17, 3362-3365
1520637 CIFC21 H15 F O2P 1 21/c 112.0845; 5.9453; 22.597
90; 103.246; 90
1580.3Du, Xiang-Wei; Stanley, Levi M.
Tandem Alkyne Hydroacylation and Oxo-Michael Addition: Diastereoselective Synthesis of 2,3-Disubstituted Chroman-4-ones and Fluorinated Derivatives.
Organic letters, 2015, 17, 3276-3279
1520655 CIFC32 H38 O5 Si2P 1 21/c 19.2692; 9.7098; 34.752
90; 92.266; 90
3125.3Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520656 CIFC16 H17 Cl O5P -16.9648; 7.7685; 14.728
76.228; 76.658; 84.002
752.04Zimmerman, Jake R.; Johntony, Olivia; Steigerwald, Daniel; Criss, Cody; Myers, Brian J.; Kinder, David H.
The Synthesis of a New Class of Highly Fluorescent Chromones via an Inverse-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3256-3259
1520657 CIFC18 H17 Br O5P 1 21 15.6762; 10.5443; 14.1611
90; 100.294; 90
833.92Sinha, Debarshi; Biswas, Arnab; Singh, Vinod K.
Chiral Phosphine-Silver(I) Complex Catalyzed Enantioselective Interrupted Feist-Bénary Reaction with Ynones: The Aldol-Cycloisomerization Cascade.
Organic letters, 2015, 17, 3302-3305
1520658 CIFC19 H20 N2 O6P 21 21 215.8624; 9.6327; 31.868
90; 90; 90
1799.61Chen, Shi; Ibrahim, Ahmad A.; Mondal, Mukulesh; Magee, Anthony J.; Cruz, Adam J.; Wheeler, Kraig A.; Kerrigan, Nessan J.
Asymmetric Synthesis of Deoxypropionate Derivatives via Catalytic Hydrogenolysis of Enantioenriched Z-Ketene Heterodimers.
Organic letters, 2015, 17, 3248-3251
1520659 CIFC22 H32 Cl2 I2 Si2P 1 21/n 113.1915; 9.4009; 22.0383
90; 106.275; 90
2623.49Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520660 CIFC16 H10 Cl2 I2P b c a9.0806; 15.5457; 23.2185
90; 90; 90
3277.6Sproul, Kyle C.; Chalifoux, Wesley A.
Highly Regio- and Diastereoselective Formation of Tetrasubstituted (Z)-1,2-Dihaloalkenes from the Halogenation of Trimethylsilyl Alkynes with ICl.
Organic letters, 2015, 17, 3334-3337
1520682 CIFC26 H19 N3 O5 SP -110.4761; 10.8361; 11.3358
76.911; 61.867; 86.563
1103.68Rao, Wei-Hao; Zhan, Bei-Bei; Chen, Kai; Ling, Peng-Xiang; Zhang, Zhuo-Zhuo; Shi, Bing-Feng
Pd(II)-Catalyzed Direct Sulfonylation of Unactivated C(sp(3))-H Bonds with Sodium Sulfinates.
Organic letters, 2015, 17, 3552-3555
1520683 CIFC20 H24 Cl N3 OP 1 21 110.868; 6.8325; 12.6102
90; 103.793; 90
909.38Johnson, Rebecca E.; de Rond, Tristan; Lindsay, Vincent N. G.; Keasling, Jay D.; Sarpong, Richmond
Synthesis of Cycloprodigiosin Identifies the Natural Isolate as a Scalemic Mixture.
Organic letters, 2015, 17, 3474-3477
1520684 CIFC13 H17 Cl O3P n a 2128.508; 5.4891; 8.1976
90; 90; 90
1282.79Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520685 CIFC21 H21 Cl O4P b c a15.5081; 11.7102; 20.245
90; 90; 90
3676.6Tanveer, Kashif; Jarrah, Kareem; Taylor, Mark S.
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols.
Organic letters, 2015, 17, 3482-3485
1520686 CIFC33 H30 N2 O6 S2P -110.7946; 12.4093; 13.1553
76.627; 68.739; 81.216
1593.12Yan, Xiaonan; Ling, Fei; Zhang, Yuchen; Ma, Cheng
Three-Component Functionalized Dihydropyridine Synthesis via a Formal Inverse Electron-Demand Hetero-Diels-Alder Reaction.
Organic letters, 2015, 17, 3536-3539
1520694 CIFC33 H27 N3 O13P -111.319; 12.665; 14.597
86.284; 86.306; 68.207
1937.1Chen, Ji-Peng; He, Wei; Yang, Zhen-Yu; Yao, Zhu-Jun
Synthesis of Tricyclo[4,3,1,0(1,5)]decane Core of Plumisclerin A Using Pauson-Khand Annulation and SmI2-Mediated Radical Cyclization.
Organic letters, 2015, 17, 3379-3381
1520702 CIFC41 H60 N8 O3 Ti2P 1 21/n 119.8643; 9.0349; 24.8875
90; 106.793; 90
4276.1Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520703 CIFC163 H221 N28 O13 Ti4P -119.976; 20.518; 21.236
89.583; 78.919; 76.303
8292Chen, Zhou; Liu, Jinna; Pei, Hao; Liu, Wei; Chen, Yanmei; Wu, Jian; Li, Wu; Li, Yahong
Directed Amination of Aryl Methyl Ethers Mediated by Ti(NMe2)4 at Room Temperature.
Organic letters, 2015, 17, 3406-3409
1520704 CIFC22 H20 N2 O3P -111.7148; 11.8534; 14.1205
110; 95.83; 100.677
1781.51Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520705 CIFC22 H22 N2 O3P c a 2117.651; 15.5231; 13.7865
90; 90; 90
3777.48Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520706 CIFC22 H20 N2 O3P 1 21/n 115.2406; 5.6664; 20.6863
90; 94.254; 90
1781.53Dörr, Aurélie A; Lubell, William D.
γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate.
Organic letters, 2015, 17, 3592-3595
1520707 CIFC20 H23 N O8P 21 21 218.7215; 11.3257; 19.217
90; 90; 90
1898.2Paladino, Marco; Zaifman, Joshua; Ciufolini, Marco A.
Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol.
Organic letters, 2015, 17, 3422-3425
1520708 CIFC15 H15 N3 O4P 1 21/n 111.4762; 7.95324; 16.5869
90; 107.894; 90
1440.7Wang, Qi; Tang, Xuli; Luo, Xiangchao; de Voogd, Nicole J.; Li, Pinglin; Li, Guoqiang
(+)- and (-)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata.
Organic letters, 2015, 17, 3458-3461
1520726 CIFC44 H42 F6 N6 O7 S2P b c a21.512; 10.424; 40.881
90; 90; 90
9167Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520727 CIFC28 H23 F3 N2 O3P -18.882; 10.743; 14.629
87; 76.43; 65.66
1234.8Zhu, Chuan-Le; Yang, Li-Jun; Li, Shen; Zheng, Yan; Ma, Jun-An
Brine-Stabilized 2,2,2-Trifluorodiazoethane and Its Application in the Synthesis of CF3-Substituted Cyclopropane α-Amino Acids.
Organic letters, 2015, 17, 3442-3445
1520728 CIFC25 H34 N2 O9 SiP b c a10.3059; 20.6482; 25.5756
90; 90; 90
5442.4Cheng, Qing-Qing; Qian, Yu; Zavalij, Peter Y.; Doyle, Michael P.
Lewis Acid/Rhodium-Catalyzed Formal [3 + 3]-Cycloaddition of Enoldiazoacetates with Donor-Acceptor Cyclopropanes.
Organic letters, 2015, 17, 3568-3571
1520729 CIFC25 H31 N O3 S2P 1 21 16.6067; 19.709; 9.7407
90; 109.22; 90
1197.65Fernández-Valparís, Javier; Romo, Juan Manuel; Romea, Pedro; Urpí, Fèlix; Kowalski, Hubert; Font-Bardia, Mercè
Stereoselective Alkylation of (S)-N-Acyl-4-isopropyl-1,3-thiazolidine-2-thiones Catalyzed by (Me3P)2NiCl2.
Organic letters, 2015, 17, 3540-3543
1520753 CIFC13 H13 Cl N2 O2 SP 1 21/c 115.767; 5.759; 15.721
90; 112.32; 90
1320.5Lu, Lei; Ma, Juan; Qu, Panpan; Li, Feng
Effective Recognition of Different Types of Amino Groups: From Aminobenzenesulfonamides to Amino-(N-alkyl)benzenesulfonamides via Iridium-Catalyzed N-Alkylation with Alcohols.
Organic letters, 2015, 17, 2350-2353
1520754 CIFC23 H21 N O3 S2P -17.667; 8.7269; 17.0497
88.1161; 89.15; 62.1966
1008.54Miura, Tomoya; Funakoshi, Yuuta; Fujimoto, Yoshikazu; Nakahashi, Junki; Murakami, Masahiro
Facile synthesis of 2,5-disubstituted thiazoles from terminal alkynes, sulfonyl azides, and thionoesters.
Organic letters, 2015, 17, 2454-2457
1520755 CIFC270 H372 B6 N8 O30C 1 2/c 152.579; 21.835; 29.598
90; 117.54; 90
30130Danjo, Hiroshi; Kidena, Yuki; Kawahata, Masatoshi; Sato, Hiroyasu; Katagiri, Kosuke; Miyazawa, Toshifumi; Yamaguchi, Kentaro
Multilayered inclusion nanocycles of anionic spiroborates.
Organic letters, 2015, 17, 2466-2469
1520756 CIFC28 H44 O4 Si2P 21 21 217.702; 13.1321; 27.4999
90; 90; 90
2781.4Shi, Hang; Tan, Ceheng; Zhang, Weibin; Zhang, Zichun; Long, Rong; Luo, Tuoping; Yang, Zhen
Synthetic Progress toward Azadirachtins. 1. Enantio- and Diastereoselective Synthesis of the Left-Wing Fragment of 11-epi-Azadirachtin I.
Organic letters, 2015, 17, 2342-2345
1520757 CIFC24 H20 O3P 1 21/c 117.7328; 8.7774; 13.0228
90; 110.419; 90
1899.61Li, Mingliang; Yang, Yudong; Zhou, Danni; Wan, Danyang; You, Jingsong
Nickel-Catalyzed Addition-Type Alkenylation of Unactivated, Aliphatic C-H Bonds with Alkynes: A Concise Route to Polysubstituted γ-Butyrolactones.
Organic letters, 2015, 17, 2546-2549
1520758 CIFC22 H33 N O9P -19.9044; 11.8847; 11.9608
60.57; 81.21; 75.803
1187.9Xu, Sanjia; Ciufolini, Marco A.
Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.
Organic letters, 2015, 17, 2424-2427
1520759 CIFC19 H27 N O10P -110.5221; 10.6666; 10.7161
74.105; 73.746; 61.845
1003.6Xu, Sanjia; Ciufolini, Marco A.
Formal Synthesis of (±)-Tetrodotoxin via the Oxidative Amidation of a Phenol: On the Structure of the Sato Lactone.
Organic letters, 2015, 17, 2424-2427
1520760 CIFC22 H36 O3P 21 21 218.1087; 11.9482; 20.232
90; 90; 90
1960.2Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng
Concise synthesis of the core structures of saundersiosides.
Organic letters, 2015, 17, 2346-2349
1520761 CIFC26 H40 O5P 21 21 217.3909; 12.9276; 25.254
90; 90; 90
2412.9Cheng, Shou-Ling; Jiang, Xiao-Ling; Shi, Yong; Tian, Wei-Sheng
Concise synthesis of the core structures of saundersiosides.
Organic letters, 2015, 17, 2346-2349
1520762 CIFC18 H23 N O4P 21 21 215.2667; 15.2534; 20.3019
90; 90; 90
1630.95Lin, Cheng-Wei; Hong, Bor-Cherng; Chang, Wan-Chen; Lee, Gene-Hsiang
A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis.
Organic letters, 2015, 17, 2314-2317
1523614 CIFC16 H13 N O4C 1 2/c 124.4884; 7.9625; 18.5286
90; 131.954; 90
2686.8Verma, Akhilesh K.; Danodia, Abhinandan K.; Saunthwal, Rakesh K.; Patel, Monika; Choudhary, Deepak
Palladium-Catalyzed Triple Successive C-H Functionalization: Direct Synthesis of Functionalized Carbazoles from Indoles.
Organic letters, 2015, 17, 3658-3661
1529193 CIFC23 H20 Br N O2P -19.823; 10.177; 11.186
92.48; 113.89; 100.8
995.5Sha, Qiang; Arman, Hadi; Doyle, Michael P.
Three-Component Cascade Reactions with 2,3-Diketoesters: A Novel Metal-Free Synthesis of 5-Vinyl-pyrrole and 4-Hydroxy-indole Derivatives.
Organic letters, 2015, 17, 3876-3879
1529249 CIFC13 H18 N2 O4P 1 21/n 19.4119; 7.6136; 18.3824
90; 104.166; 90
1277.2Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep
Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones.
Organic letters, 2015, 17, 3860-3863
1529250 CIFC16 H16 Cl N O2P n a 217.9657; 14.5166; 12.0126
90; 90; 90
1389.08Diaba, Faïza; Montiel, Juan A.; Serban, Georgeta; Bonjoch, Josep
Synthesis of Normorphans through an Efficient Intramolecular Carbamoylation of Ketones.
Organic letters, 2015, 17, 3860-3863
1529257 CIFC19 H20 N2 O5 SP 1 21 111.1369; 12.7954; 13.7775
90; 105.869; 90
1888.49Feng, Huan-Xi; Tan, Rui; Liu, Yan-Kai
An Efficient One-Pot Approach to the Construction of Chiral Nitrogen-Containing Heterocycles under Mild Conditions.
Organic letters, 2015, 17, 3794-3797
1529280 CIFC17 H13 NP 1 21/c 18.8383; 21.101; 6.6024
90; 91.311; 90
1231Mandal, Sumana; Mahato, Sujit; Jana, Chandan K.
Direct β-C(sp(3))-H Functionalization of Aliphatic Amines to α,β-Unsaturated Imines, Aldehydes, and Chromenes.
Organic letters, 2015, 17, 3762-3765
1529281 CIFC24 H21 N O4 SP 1 21/c 117.7457; 5.8725; 20.1502
90; 103.189; 90
2044.5Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones.
Organic letters, 2015, 17, 3846-3849
1529282 CIFC17 H13 Br O2P n a 2129.2958; 6.1415; 15.5413
90; 90; 90
2796.2Kuppusamy, Ramajayam; Gandeepan, Parthasarathy; Cheng, Chien-Hong
Rh(III)-Catalyzed [4 + 1] Annulations of 2-Hydroxy- and 2-Aminobenzaldehydes with Allenes: A Simple Method toward 3-Coumaranones and 3-Indolinones.
Organic letters, 2015, 17, 3846-3849
1529283 CIFC18 H27 N O4P 21 21 2110.1466; 10.1835; 16.6612
90; 90; 90
1721.57Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin
Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.
Organic letters, 2015, 17, 3938-3940
1529284 CIFC17 H27 N O2P 1 21 18.2578; 7.6701; 12.4589
90; 99.389; 90
778.55Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin
Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.
Organic letters, 2015, 17, 3938-3940
1529285 CIFC18 H25 N O4P 1 21 18.5383; 7.6057; 12.8523
90; 104.589; 90
807.71Lin, Kuo-Wei; Ananthan, Bakthavachalam; Tseng, Sheng-Fang; Yan, Tu-Hsin
Exceedingly Concise and Elegant Synthesis of (+)-Paniculatine, (-)-Magellanine, and (+)-Magellaninone.
Organic letters, 2015, 17, 3938-3940
1529293 CIFC21 H22 N2 O2P 21 21 218.8494; 10.974; 17.557
90; 90; 90
1705Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi
Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.
Organic letters, 2015, 17, 3918-3921
1529294 CIFC22 H20 N2 OP -110.3796; 12.9633; 14.3864
71.474; 71.763; 68.137
1661.2Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi
Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.
Organic letters, 2015, 17, 3918-3921
1529307 CIFC29 H36 O7 SiP 1 21/c 114.1631; 11.4869; 16.4977
90; 94.808; 90
2674.57Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke
Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.
Organic letters, 2015, 17, 3746-3749
1529349 CIFC36 H62 Cl2 Cu2 O6 P2 S2P 1 21 110.6416; 13.3076; 17.3445
90; 92.328; 90
2454.2Wang, Ding; Cao, Peng; Wang, Bing; Jia, Tao; Lou, Yazhou; Wang, Min; Liao, Jian
Copper(I)-Catalyzed Asymmetric Pinacolboryl Addition of N-Boc-imines Using a Chiral Sulfoxide-Phosphine Ligand.
Organic letters, 2015, 17, 2420-2423
1529350 CIFC16 H10 Br F3 N2 O2 SI 1 2/a 111.4371; 13.3473; 22.4306
90; 101.301; 90
3357.74Lee, Eunsook; Ryu, Taekyu; Shin, Eunji; Son, Jeong-Yu; Choi, Wonseok; Lee, Phil Ho
Synthesis of 2-bromoimidazoles from alkynes, N-sulfonylazides, and bromocyanides.
Organic letters, 2015, 17, 2470-2473
1529362 CIFC32 H22 N6P 1 21/c 115.6612; 9.6881; 16.3377
90; 96.112; 90
2464.8Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.
Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.
Organic letters, 2015, 17, 4026-4029
1529363 CIFC34 H26 Cl2 N6P -18.8511; 9.8863; 16.5742
107.267; 92.876; 90.368
1382.87Constantinides, Christos P.; Zissimou, Georgia A.; Berezin, Andrey A.; Ioannou, Theodosia A.; Manoli, Maria; Tsokkou, Demetra; Theodorou, Eleni; Hayes, Sophia C.; Koutentis, Panayiotis A.
Tetraphenylhexaazaanthracenes: 16π Weakly Antiaromatic Species with Singlet Ground States.
Organic letters, 2015, 17, 4026-4029
1529370 CIFC22 H18 F3 N O4 SP 1 21/c 115.9; 21.601; 19.802
90; 110.332; 90
6377.4Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529371 CIFC28 H24 F3 N O5 SP -112.978; 13.576; 16.636
84.126; 79.909; 65.828
2631.2Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529372 CIFC28 H24 F3 N O4 SP 1 21/n 115.6589; 9.9834; 16.2519
90; 92.274; 90
2538.6Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529373 CIFC24 H24 F3 N O4 SP -110.562; 11.1083; 11.2554
85.47; 66.868; 84.789
1208Xin, Xiaoyi; Wang, Haolong; Li, Xincheng; Wang, Dongping; Wan, Boshun
Base-Catalyzed Selective Synthesis of 2-Azabicyclo[3.2.0]hept-2-enes and Sulfonyl Vinyl-Substituted Pyrroles from 3-Aza-1,5-enynes.
Organic letters, 2015, 17, 3944-3947
1529374 CIFC22 H20 N2 O2 SP 1 21/c 111.5958; 12.0999; 14.031
90; 97.891; 90
1950Zeng, Ting-Ting; Xuan, Jun; Ding, Wei; Wang, Kuan; Lu, Liang-Qiu; Xiao, Wen-Jing
[3 + 2] Cycloaddition/Oxidative Aromatization Sequence via Photoredox Catalysis: One-Pot Synthesis of Oxazoles from 2H-Azirines and Aldehydes.
Organic letters, 2015, 17, 4070-4073
1529381 CIFC114 H172 Cl K Li0 N47 O38C 1 2/c 129.3719; 14.1615; 33.703
90; 101.172; 90
13753.1Lu, Xiaoyong; Isaacs, Lyle
Synthesis and Recognition Properties of Enantiomerically Pure Acyclic Cucurbit[n]uril-Type Molecular Containers.
Organic letters, 2015, 17, 4038-4041
1529393 CIFC25 H24 Cl N O5P 21 21 216.9051; 18.0332; 18.2794
90; 90; 90
2276.2Liu, Qiong-Jie; Yan, Wen-Guang; Wang, Lijia; Zhang, X. Peter; Tang, Yong
One-Pot Catalytic Asymmetric Synthesis of Tetrahydrocarbazoles.
Organic letters, 2015, 17, 4014-4017
1529398 CIFC25 H23 N O6C 1 2/c 131.5153; 8.7548; 18.0436
90; 123.435; 90
4154.5Huang, Jing-Kai; Yang Lauderdale, Tsai-Ling; Shia, Kak-Shan
Studies on Antibiotics Active against Resistant Bacteria. Total Synthesis of MRSA-Active Tetarimycin A and Its Analogues.
Organic letters, 2015, 17, 4248-4251
1529399 CIFC55 H35 B F2 N2P 1 21/c 116.4511; 17.491; 13.5624
90; 98.856; 90
3856Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan
Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.
Organic letters, 2015, 17, 4168-4171
1529400 CIFC55 H36 B F7 N2P 1 21/c 113.1321; 10.7218; 30.2961
90; 96.85; 90
4235.23Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan
Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.
Organic letters, 2015, 17, 4168-4171
1529401 CIFC55 H41 B F2 N2C 1 2/c 121.491; 13.7296; 29.3488
90; 106.144; 90
8318.3Chua, Ming Hui; Huang, Kuo-Wei; Xu, Jianwei; Wu, Jishan
Unusual Intramolecular Hydrogen Transfer in 3,5-Di(triphenylethylenyl) BODIPY Synthesis and 1,2-Migratory Shift in Subsequent Scholl Type Reaction.
Organic letters, 2015, 17, 4168-4171
1529402 CIFC19 H20 Br N OP 1 21 15.225; 13.44; 11.8487
90; 90.133; 90
832.06Dziechciejewski, Wojciech J.; Weber, Regina; Sowada, Oliver; Boysen, Mike M. K.
Cycloalkene Carbonitriles in Rhodium-Catalyzed 1,4-Addition and Formal Synthesis of Vabicaserin.
Organic letters, 2015, 17, 4132-4135
1529420 CIFC21 H23 Cl F2 N2 OC 1 c 113.1195; 25.1207; 6.0786
90; 103.299; 90
1949.6Chen, Qiao; Zhou, Jiawei; Wang, Yanan; Wang, Chao; Liu, Xihong; Xu, Zhaoqing; Lin, Li; Wang, Rui
Transition-Metal-Free Dehydrosilylative Difluoroamidation of Tetrahydroisoquinolines under Mild Conditions.
Organic letters, 2015, 17, 4212-4215
1529421 CIFC13 H18 O4P 1 21 15.917; 7.864; 13.651
90; 101.24; 90
623Rybak, Taras; Hall, Dennis G.
Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B.
Organic letters, 2015, 17, 4156-4159
1529422 CIFC13 H18 O3P 1 21/n 19.7101; 10.6909; 23.0359
90; 92.6548; 90
2388.78Rybak, Taras; Hall, Dennis G.
Stereoselective and Regiodivergent Allylic Suzuki-Miyaura Cross-Coupling of 2-Ethoxydihydropyranyl Boronates: Synthesis and Confirmation of Absolute Stereochemistry of Diospongin B.
Organic letters, 2015, 17, 4156-4159
1529423 CIFC42 H33 Cl2 Ir N2 O5P 1 21/n 118.021; 10.891; 18.559
90; 103.69; 90
3539Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan
Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone.
Organic letters, 2015, 17, 4204-4207
1529424 CIFC28 H18 Cl2 N2 O5P -110.069; 10.87; 12.021
71.67; 82.11; 82.87
1232.5Zhou, Tao; Li, Liubo; Li, Bin; Song, Haibin; Wang, Baiquan
Ir(III)-Catalyzed Oxidative Coupling of NH Isoquinolones with Benzoquinone.
Organic letters, 2015, 17, 4204-4207
1529448 CIFC15 H18 Cl N O2P -111.1941; 11.9877; 12.3151
117.921; 101.02; 90.422
1424.3Deng, Yongming; Jing, Changcheng; Zavalij, Peter Y.; Doyle, Michael P.
Hg(OTf)2 Catalyzed Intramolecular 1,4-Addition of Donor-Acceptor Cyclopropenes to Arenes.
Organic letters, 2015, 17, 4312-4315
1529469 CIFC22 H35 N O3P 21 21 216.212; 12.231; 28.133
90; 90; 90
2137.5Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui
Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.
Organic letters, 2015, 17, 4304-4307
1529470 CIFC22 H33 N O3.5P 21 21 2112.515; 14.907; 45.898
90; 90; 90
8563Zhang, Dewu; Tao, Xiaoyu; Chen, Ridao; Liu, Jimei; Li, Li; Fang, Xiaomei; Yu, Liyan; Dai, Jungui
Pericoannosin A, a Polyketide Synthase-Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.
Organic letters, 2015, 17, 4304-4307
1529473 CIFC28 H29 N5 O4P -17.7823; 10.8987; 15.2414
72.781; 83.016; 85.094
1224Samanta, Ritwik; Kumar, B. Sathish; Panda, Pradeepta K.
Calix[4]pyrroles with Shortest Possible Strap: Exclusively Selective toward Fluoride Ion.
Organic letters, 2015, 17, 4140-4143
1529503 CIFC25 H22 Cl3 F3 N2 O2 SP -18.374; 10.228; 16.064
99.954; 98.372; 101.416
1305.1Wei, Qiang; Chen, Jia-Rong; Hu, Xiao-Qiang; Yang, Xiao-Chen; Lu, Bin; Xiao, Wen-Jing
Photocatalytic Radical Trifluoromethylation/Cyclization Cascade: Synthesis of CF3-Containing Pyrazolines and Isoxazolines.
Organic letters, 2015, 17, 4464-4467
1529847 CIFC21 H22 N2 O2P 1 21 19.702; 7.4213; 12.862
90; 103.265; 90
901.4Komine, Keita; Nomura, Yusuke; Ishihara, Jun; Hatakeyama, Susumi
Total Synthesis of (-)-N-Methylwelwitindolinone C Isothiocyanate Based on a Pd-Catalyzed Tandem Enolate Coupling Strategy.
Organic letters, 2015, 17, 3918-3921
1529848 CIFC17 H20 O6P 1 21/c 113.5566; 9.9192; 12.1878
90; 114.983; 90
1485.55Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke
Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.
Organic letters, 2015, 17, 3746-3749
1529849 CIFC37 H54 O6 SiP 1 21/c 19.8958; 32.0974; 20.6189
90; 92.873; 90
6540.9Sakata, Juri; Ando, Yoshio; Ohmori, Ken; Suzuki, Keisuke
Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle.
Organic letters, 2015, 17, 3746-3749
1529850 CIFC16 H12 Br F2 N3P 1 21/c 115.027; 8.8571; 11.123
90; 96.542; 90
1470.8Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio
Difluoromethylation of Terminal Alkynes by Fluoroform.
Organic letters, 2015, 17, 3802-3805
1529851 CIFC16 H10 Br F2 N OP 1 21/n 117.957; 6.8848; 22.81
90; 99.781; 90
2779Okusu, Satoshi; Tokunaga, Etsuko; Shibata, Norio
Difluoromethylation of Terminal Alkynes by Fluoroform.
Organic letters, 2015, 17, 3802-3805
1529852 CIFC43 H37 Br2 Cl Cu N3 O4 P2P n a 2119.3661; 14.8237; 28.5913
90; 90; 90
8207.9Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan
Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst.
Organic letters, 2015, 17, 3814-3817
1529853 CIFC17 H19 N O3P -15.7487; 9.5873; 13.7161
85.932; 86.522; 90.042
752.65Ramakrishna, Kankanala; Murali, Mani; Sivasankar, Chinnappan
Chemoselective Carbene insertion into the N-H Bond over O-H Bond Using a Well-Defined Single Site (P-P)Cu(I) Catalyst.
Organic letters, 2015, 17, 3814-3817
1529854 CIFC18 H16 Br N O3 SP 21 21 217.9153; 11.4655; 18.152
90; 90; 90
1647.3Xiao, Yonglong; Wang, Jinxin; Xia, Wenjing; Shu, Shuangjie; Jiao, Shenchao; Zhou, Yu; Liu, Hong
γ-Carbon Activation through N-Heterocyclic Carbene/Brønsted Acids Cooperative Catalysis: A Highly Enantioselective Route to δ-Lactams.
Organic letters, 2015, 17, 3850-3853
1529855 CIFC26 H18 N2 O SP 1 21/n 19.919; 19.032; 11.221
90; 102.942; 90
2064.5Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli
A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones.
Organic letters, 2015, 17, 3872-3875
1529856 CIFC29 H21 Br N2 OP -19.724; 11.142; 12.91
98.826; 103.604; 112.844
1205.2Zhu, Yuelu; Li, Cheng; Zhang, Jidong; She, Mengyao; Sun, Wei; Wan, Kerou; Wang, Yaqi; Yin, Bin; Liu, Ping; Li, Jianli
A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones.
Organic letters, 2015, 17, 3872-3875
1529857 CIFC20 H22 N2 O5 SP 21 21 216.8305; 13.7709; 21.5589
90; 90; 90
2027.88Rao, Wei-Hao; Yin, Xue-Song; Shi, Bing-Feng
Catalyst-Controlled Amino- versus Oxy-Acetoxylation of Urea-Tethered Alkenes: Efficient Synthesis of Cyclic Ureas and Isoureas.
Organic letters, 2015, 17, 3758-3761

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