Crystallography Open Database

Result: there are 1579 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Chemical Communications' volume of publication is 48

Blue left arrow Blue left arrow First | Blue left arrow Previous 20 | of 79 | Next 20 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
7107749 CIFC60 H78 Dy K N8 O8P 1 21/m 111.5601; 17.6684; 14.8072
90; 105.726; 90
2911.1Ursula J.Williams; Brian D. Mahoney; Patrick T. DeGregorio; Patrick Carroll; Eiko Nakamaru-Ogiso; James M.Kikkawa; Eric J. Schelter
A comparison of the effects of symmetry and magnetoanisotropy on paramagnetic relaxation in related dysprosium single ion magnets
Chem.Commun., 2012, 48, 5593
7107750 CIFC52 H64 Dy K N8 O4P 1 2/c 123.03; 11.422; 44.36
90; 91.414; 90
11665Ursula J.Williams; Brian D. Mahoney; Patrick T. DeGregorio; Patrick Carroll; Eiko Nakamaru-Ogiso; James M.Kikkawa; Eric J. Schelter
A comparison of the effects of symmetry and magnetoanisotropy on paramagnetic relaxation in related dysprosium single ion magnets
Chem.Commun., 2012, 48, 5593
7107751 CIFC25 H24 Cl3 F N4 O PdP -19.5854; 10.369; 14.3676
83.969; 71.762; 72.577
1293.95Jhen-Yi Lee; Yao-Huei Huang; Shu-Ya Liu; Shun-Chu Cheng; Yang-Ming Jhou; Jenn-Huei Lii; Hon Man Lee
Formation of CC-type palladacycles with assistance from an apparently innocent NH(CO) functional group
Chem.Commun., 2012, 48, 5632
7107752 CIFC37 H32 Cl F N3 O P PdP -19.334; 10.4256; 18.9156
80.502; 77.272; 68.741
1665.96Jhen-Yi Lee; Yao-Huei Huang; Shu-Ya Liu; Shun-Chu Cheng; Yang-Ming Jhou; Jenn-Huei Lii; Hon Man Lee
Formation of CC-type palladacycles with assistance from an apparently innocent NH(CO) functional group
Chem.Commun., 2012, 48, 5632
7107753 CIFC42 H44 Cl F N4 O2.5 P PdP -114.5982; 16.6492; 17.5208
81.635; 70.792; 82.732
3964.4Jhen-Yi Lee; Yao-Huei Huang; Shu-Ya Liu; Shun-Chu Cheng; Yang-Ming Jhou; Jenn-Huei Lii; Hon Man Lee
Formation of CC-type palladacycles with assistance from an apparently innocent NH(CO) functional group
Chem.Commun., 2012, 48, 5632
7107754 CIFC34 H29 Cl3 N4 O PdP -19.8587; 11.1511; 15.017
80.665; 89.264; 73.218
1558.65Jhen-Yi Lee; Yao-Huei Huang; Shu-Ya Liu; Shun-Chu Cheng; Yang-Ming Jhou; Jenn-Huei Lii; Hon Man Lee
Formation of CC-type palladacycles with assistance from an apparently innocent NH(CO) functional group
Chem.Commun., 2012, 48, 5632
7107755 CIFC49 H44 Cl N4 O2 P PdP -112.507; 13.088; 14.438
103.747; 115.434; 90.425
2057Jhen-Yi Lee; Yao-Huei Huang; Shu-Ya Liu; Shun-Chu Cheng; Yang-Ming Jhou; Jenn-Huei Lii; Hon Man Lee
Formation of CC-type palladacycles with assistance from an apparently innocent NH(CO) functional group
Chem.Commun., 2012, 48, 5632
7107756 CIFC52 H66 Cl2 F2 N10 O6 Pd2P -19.4686; 11.5276; 13.1627
90.963; 106.242; 94.606
1373.8Jhen-Yi Lee; Yao-Huei Huang; Shu-Ya Liu; Shun-Chu Cheng; Yang-Ming Jhou; Jenn-Huei Lii; Hon Man Lee
Formation of CC-type palladacycles with assistance from an apparently innocent NH(CO) functional group
Chem.Commun., 2012, 48, 5632
7107757 CIFC19 H16 Br N O2P 21 21 215.2806; 8.1975; 37.8235
90; 90; 90
1637.29Utpal Das; Chan-Hui Huang; Wenwei Lin
Enantioselective synthesis of substituted pyrans via amine-catalyzed Michael addition and subsequent enolization/cyclisation
Chem.Commun., 2012, 48, 5590
7107758 CIFC22 H20 Br N O2P 21 21 215.5785; 15.6744; 22.2663
90; 90; 90
1947Utpal Das; Chan-Hui Huang; Wenwei Lin
Enantioselective synthesis of substituted pyrans via amine-catalyzed Michael addition and subsequent enolization/cyclisation
Chem.Commun., 2012, 48, 5590
7107759 CIFC12 H14 N2 O6C 1 2 111.1949; 6.3676; 18.385
90; 105.512; 90
1262.8Christopher S. Theile; Larry W. McLaughlin
An Efficient Synthetic Approach to 6,5' (<i>S</i>) and 6,5' (<i>R</i>) - Cyclouridine
Chem.Commun., 2012, 48, 5587
7107760 CIFC13 H16 N2 O9P 1 21 19.549; 7.829; 10.026
90; 108.14; 90
712.3Christopher S. Theile; Larry W. McLaughlin
An Efficient Synthetic Approach to 6,5' (<i>S</i>) and 6,5' (<i>R</i>) - Cyclouridine
Chem.Commun., 2012, 48, 5587
7107761 CIFC28 H24 Cl N O2 SP 1 21 112.29; 5.9017; 16.991
90; 104.225; 90
1194.6Honggang Cheng; Liang-Qiu Lu; Tao Wang; Jia-Rong Chen; Wen-Jing Xiao
Design of chiral sulfoxide-Schiff base hybrids and their application in Cu-catalyzed asymmetric Henry reactions
Chem.Commun., 2012, 48, 5596
7107762 CIFC88 H72P 1 21/n 116.1189; 9.4946; 21.3361
90; 100.876; 90
3206.7Akihiro Shimizu; Yasukazu Hirao; Kozo Matsumoto; Hiroyuki Kurata; Takashi Kubo; Mikio Uruichi; Kyuya Yakushi
Aromaticity and pi-bond covalency: Strong intermolecular covalent bonding interaction of a Kekule hydrocarbon with very large singlet biradical character
Chem.Commun., 2012, 48, 5629
7107763 CIFC78 H52P -110.152; 11.5617; 11.94
90.925; 96.852; 108.851
1314.6Akihiro Shimizu; Yasukazu Hirao; Kozo Matsumoto; Hiroyuki Kurata; Takashi Kubo; Mikio Uruichi; Kyuya Yakushi
Aromaticity and pi-bond covalency: Strong intermolecular covalent bonding interaction of a Kekule hydrocarbon with very large singlet biradical character
Chem.Commun., 2012, 48, 5629
7107764 CIFC30 H26 Cl2 OP -110.012; 10.685; 11.953
102.786; 91.396; 100.23
1224.5Huanhuan Wang; Yong Luo; Biao Zhu; Jie Wu
Generation of cyclopenta[c]chromenes via a palladium-catalyzed reaction of 2-alkynylphenol with 2-alkynylvinyl bromide
Chem.Commun., 2012, 48, 5581
7107766 CIFC32 H34 N2 O6P 1 21/c 114.93; 9.11; 21.95
90; 106.81; 90
2858Masaki Yamamura; Yuki Okazaki; Tatsuya Nabeshima
Locking of Photoisomerization Behavior of Self-assemble Azobenzene-linked Macrocycles with Structural Restriction
Chem.Commun., 2012, 48, 5724
7107767 CIFC11 H11 Br O2P 1 21 18.7478; 11.7579; 10.7912
90; 106.206; 90
1065.83Chong Kiat Tan; Chen Cheng Le; Ying-Yeung Yeung
Enantioselective bromolactonization of cis-1,2-disubstituted olefinic acids using an amino-thiocarbamate catalyst
Chem.Commun., 2012, 48, 5793
7107768 CIFC13 H18 N4 O4P 1 21/c 112.4949; 7.7324; 14.7304
90; 92.741; 90
1421.6Philipp A. Ottersbach; Gregor Schnakenburg; Michael Gutschow
Induction of chirality: experimental evidence of atropisomerism in azapeptides
Chem.Commun., 2012, 48, 5772
7107769 CIFC12 H16 N4 O4P -14.8613; 11.6939; 11.7674
99.755; 94.085; 90.661
657.41Philipp A. Ottersbach; Gregor Schnakenburg; Michael Gutschow
Induction of chirality: experimental evidence of atropisomerism in azapeptides
Chem.Commun., 2012, 48, 5772

Blue left arrow Blue left arrow First | Blue left arrow Previous 20 | of 79 | Next 20 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

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