Crystallography Open Database

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Searching journal of publication like 'Organic Letters' volume of publication is 7

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1506765 CIFC61 H64 B2 S2P -18.0399; 14.829; 22.669
105.23; 100.18; 93.56
2549.9Liu, Zhi-Qiang; Shi, Mei; Li, Fu-You; Fang, Qi; Chen, Zhang-Hai; Yi, Tao; Huang, Chun-Hui
Highly selective two-photon chemosensors for fluoride derived from organic boranes.
Organic letters, 2005, 7, 5481-5484
1506766 CIFC34 H40 Fe2 N2 O4P 21 21 219.686; 23.733; 25.31
90; 90; 90
5818Fukuzawa, Shin-ichi; Yahara, Yuusuke; Kamiyama, Akira; Hara, Masumi; Kikuchi, Satoshi
Stereoselective pinacol coupling of chiral formylferrocene using divalent samarium triflate: preparation of a new chiral bisferrocenyl oxazoline ligand and its application to asymmetric Diels-Alder reactions.
Organic letters, 2005, 7, 5809-5812
1506767 CIFC34 H40 Fe2 N2 O4P 1 21 112.647; 11.666; 20.496
90; 95.638; 90
3009.3Fukuzawa, Shin-ichi; Yahara, Yuusuke; Kamiyama, Akira; Hara, Masumi; Kikuchi, Satoshi
Stereoselective pinacol coupling of chiral formylferrocene using divalent samarium triflate: preparation of a new chiral bisferrocenyl oxazoline ligand and its application to asymmetric Diels-Alder reactions.
Organic letters, 2005, 7, 5809-5812
1506768 CIFC30 H40 Fe2 N2 O2P 21 21 2111.484; 12.169; 18.868
90; 90; 90
2637Fukuzawa, Shin-ichi; Yahara, Yuusuke; Kamiyama, Akira; Hara, Masumi; Kikuchi, Satoshi
Stereoselective pinacol coupling of chiral formylferrocene using divalent samarium triflate: preparation of a new chiral bisferrocenyl oxazoline ligand and its application to asymmetric Diels-Alder reactions.
Organic letters, 2005, 7, 5809-5812
1506769 CIFC16 H8 Se4P 1 21/a 112.632; 7.864; 14.964
90; 101.258; 90
1457.9Okamoto, Toshihiro; Kudoh, Kenichi; Wakamiya, Atsushi; Yamaguchi, Shigehiro
General synthesis of thiophene and selenophene-based heteroacenes.
Organic letters, 2005, 7, 5301-5304
1506770 CIFC16 H8 S3P n m a7.933; 26.589; 5.906
90; 90; 90
1245.8Okamoto, Toshihiro; Kudoh, Kenichi; Wakamiya, Atsushi; Yamaguchi, Shigehiro
General synthesis of thiophene and selenophene-based heteroacenes.
Organic letters, 2005, 7, 5301-5304
1506771 CIFC13 H15 N O4P -111.014; 13.147; 4.8355
95.35; 97.18; 113.337
629.98Minami, Kimi; Kawamura, Yasufumi; Koga, Koichi; Hosokawa, Takahiro
Palladium(II)-catalyzed oxidative transformation of allylic alcohols and vinyl ethers into 2-alkoxytetrahydrofurans: catechol as an activator of catalyst.
Organic letters, 2005, 7, 5689-5692
1506772 CIFC16 H19 N O5C 1 2/c 119.238; 12.755; 15.148
90; 124.62; 90
3058.9Minami, Kimi; Kawamura, Yasufumi; Koga, Koichi; Hosokawa, Takahiro
Palladium(II)-catalyzed oxidative transformation of allylic alcohols and vinyl ethers into 2-alkoxytetrahydrofurans: catechol as an activator of catalyst.
Organic letters, 2005, 7, 5689-5692
1506773 CIFC18 H26 N2 O3P -17.6022; 9.2365; 12.431
102.263; 96.458; 100.565
828.02Sales, Marcelo; Charette, André B
A Diels-Alder approach to the stereoselective synthesis of 2,3,5,6-tetra- and 2,3,4,5,6-pentasubstituted piperidines.
Organic letters, 2005, 7, 5773-5776
1506774 CIFC24 H33 N O4C 1 c 110.685; 24.806; 8.872
90; 108.68; 90
2227.7Sales, Marcelo; Charette, André B
A Diels-Alder approach to the stereoselective synthesis of 2,3,5,6-tetra- and 2,3,4,5,6-pentasubstituted piperidines.
Organic letters, 2005, 7, 5773-5776
1506775 CIFC27 H60 O Si3P 1 21 19.2671; 14.343; 12.2312
90; 95.604; 90
1618Cleary, Pamela A.; Woerpel, K. A.
Metal-catalyzed rearrangement of homoallylic ethers to silylmethyl allylic silanes in the presence of a Di-tert-butylsilylene source.
Organic letters, 2005, 7, 5531-5533
1506776 CIFC27 H20 O6P 1 21/c 115.45; 9.102; 15.6427
90; 109.702; 90
2071Lumb, Jean-Philip; Trauner, Dirk
Pericyclic reactions of prenylated naphthoquinones: biomimetic syntheses of mollugin and microphyllaquinone.
Organic letters, 2005, 7, 5865-5868
1506777 CIFC27 H19 O6P -18.798; 9.098; 13.336
85.941; 80.845; 88.91
1051.2Lumb, Jean-Philip; Trauner, Dirk
Pericyclic reactions of prenylated naphthoquinones: biomimetic syntheses of mollugin and microphyllaquinone.
Organic letters, 2005, 7, 5865-5868
1506778 CIFC28 H31 Br O3 SiC 1 2/c 130.718; 6.6546; 26.833
90; 105.942; 90
5274.1Sasaki, Michiko; Higashi, Mariko; Masu, Hyuma; Yamaguchi, Kentaro; Takeda, Kei
Asymmetric [2,3]-Wittig rearrangement induced by a chiral carbanion whose chirality was transferred from an epoxide.
Organic letters, 2005, 7, 5913-5915
1506779 CIFC40 H41 Cl10 N2 O2 Rh SP 21 21 2114.219; 17.256; 19.305
90; 90; 90
4737Matharu, Daljit S.; Morris, David J.; Kawamoto, Aparecida M.; Clarkson, Guy J.; Wills, Martin
A stereochemically well-defined rhodium(III) catalyst for asymmetric transfer hydrogenation of ketones.
Organic letters, 2005, 7, 5489-5491
1506780 CIFC14 H19 N O3P 1 21/c 16.3947; 9.4295; 21.418
90; 96.469; 90
1283.26Lam, Hon Wai; Murray, Gordon J.; Firth, James D.
Diastereoselective synthesis of 4-hydroxypiperidin-2-ones via Cu(I)-catalyzed reductive aldol cyclization.
Organic letters, 2005, 7, 5743-5746
1506781 CIFC19 H21 N O3P 1 21/c 120.693; 5.8798; 13.1078
90; 98.577; 90
1577Lam, Hon Wai; Murray, Gordon J.; Firth, James D.
Diastereoselective synthesis of 4-hydroxypiperidin-2-ones via Cu(I)-catalyzed reductive aldol cyclization.
Organic letters, 2005, 7, 5743-5746
1506782 CIFC15 H21 N O3P 1 21/c 120.3081; 6.8444; 10.4444
90; 98.961; 90
1434.02Lam, Hon Wai; Murray, Gordon J.; Firth, James D.
Diastereoselective synthesis of 4-hydroxypiperidin-2-ones via Cu(I)-catalyzed reductive aldol cyclization.
Organic letters, 2005, 7, 5743-5746
1506783 CIFC20 H23 N O3P 1 21/c 120.655; 6.0188; 13.3363
90; 97.128; 90
1645.13Lam, Hon Wai; Murray, Gordon J.; Firth, James D.
Diastereoselective synthesis of 4-hydroxypiperidin-2-ones via Cu(I)-catalyzed reductive aldol cyclization.
Organic letters, 2005, 7, 5743-5746
1506784 CIFC17 H23 N O5P 21 21 216.4784; 9.8027; 26.807
90; 90; 90
1702.4Lam, Hon Wai; Murray, Gordon J.; Firth, James D.
Diastereoselective synthesis of 4-hydroxypiperidin-2-ones via Cu(I)-catalyzed reductive aldol cyclization.
Organic letters, 2005, 7, 5743-5746

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