Crystallography Open Database

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Searching journal of publication like 'Chem.Commun.' volume of publication is 52

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7118208 CIFC26 H25 N O2 SP 1 21/n 113.926; 10.6835; 14.955
90; 92.243; 90
2223.3Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118209 CIFC26 H27 N O3 SP 1 21/n 110.4657; 19.751; 12.477
90; 114.712; 90
2342.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118210 CIFC24 H21 N O2 SP 1 21/c 110.6663; 10.8826; 18.121
90; 103.78; 90
2042.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118211 CIFC24 H21 N O2 SP 1 21/c 114.001; 12.335; 11.587
90; 95.497; 90
1991.9Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118212 CIFC24 H21 N O2 SP 1 21/c 18.9249; 9.9995; 22.944
90; 107.13; 90
1956.8Wang, Zhiming; Xu, Xingzhu; Gu, Zhanshou; Feng, Wei; Qian, Houjun; Li, Zhengyi; Sun, Xiaoqiang; Kwon, Ohyun
Nazarov cyclization of 1,4-pentadien-3-ols: preparation of cyclopenta[b]indoles and spiro[indene-1,4'-quinoline]s.
Chemical communications (Cambridge, England), 2016, 52, 2811-2814
7118213 CIFC54 H58 N3 P2 RhP 1 21/n 113.58; 21.768; 17.29
90; 111.548; 90
4754Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118214 CIFC48 H48 N3 P2 RhP 1 21/c 116.185; 18.144; 15.477
90; 118.406; 90
3998Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118215 CIFC72 H66 N3 P2 RhP 1 21/n 113.567; 28.198; 16.293
90; 109.213; 90
5886Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118216 CIFC98 H96 N6 P4 Rh2C 1 2/c 142.986; 17.237; 27.577
90; 119.527; 90
17779Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118217 CIFC60 H56 N3 P2 RhP 1 21/n 113.907; 27.103; 16.593
90; 112.133; 90
5793Hänninen, Mikko M; Zamora, Matthew T.; MacNeil, Connor S.; Knott, Jackson P.; Hayes, Paul G.
Elucidation of the resting state of a rhodium NNN-pincer hydrogenation catalyst that features a remarkably upfield hydride (1)H NMR chemical shift.
Chemical communications (Cambridge, England), 2016, 52, 586-589
7118218 CIFC36 H26 Br2 O4P 21 21 215.6288; 12.578; 41.669
90; 90; 90
2950.1Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118219 CIFC36 H28 O4P 21 21 219.263; 12.8186; 22.369
90; 90; 90
2656.1Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118220 CIFC36 H26 Br2 O4P 21 21 215.5911; 13.004; 40.623
90; 90; 90
2953.6Wang, Zhan-Yong; Ding, Ya-Li; Wang, Gang; Cheng, Ying
Chiral N-heterocyclic carbene/Lewis acid cooperative catalysis of the reaction of 2-aroylvinylcinnamaldehydes: a switch of the reaction pathway by Lewis acid activation.
Chemical communications (Cambridge, England), 2015, 52, 788-791
7118221 CIFC13 H11 F N2P -110.0641; 11.0425; 12.1824
114.924; 95.055; 111.476
1094.39Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak
'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks.
Chemical communications (Cambridge, England), 2016, 52, 2141-2144
7118222 CIFC13 H10 F2 N2P 1 21/c 112.7028; 8.3775; 11.5509
90; 117.017; 90
1095.1Dey, Dhananjay; Thomas, Sajesh P.; Spackman, Mark A.; Chopra, Deepak
'Quasi-isostructural polymorphism' in molecular crystals: inputs from interaction hierarchy and energy frameworks.
Chemical communications (Cambridge, England), 2016, 52, 2141-2144
7118223 CIFC41 H33 N3 O6P 1 21/c 111.1829; 11.5006; 26.2259
90; 92.219; 90
3370.4Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118224 CIFC41 H33 Cd Cl0 I2 N3 O6R -3 :H54.6374; 54.6374; 8.9458
90; 90; 120
23127.6Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118225 CIFC42.17 H36 Br Cd I2 N3 O6.33R -3 :H54.5811; 54.5811; 8.9081
90; 90; 120
22982.7Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118226 CIFC42 H35 Cd I4 N3 O6R -3 :H54.772; 54.772; 8.8733
90; 90; 120
23053.3Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548
7118227 CIFC41 H33 Cd I2 N3 O6R -3 :H54.8819; 54.8819; 8.8759
90; 90; 120
23152.7Kim, Jeong Gyun; Noh, Tae Hwan; Cho, Yoonjung; Park, Jin Kyoon; Jung, Ok-Sang
A triple-function nanotube as a reactant reservoir, reaction platform, and byproduct scavenger for photo-cyclopropanation.
Chemical communications (Cambridge, England), 2016, 52, 2545-2548

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