Crystallography Open Database

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Searching journal of publication like 'Green Chem.' volume of publication is 18

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1540034 CIFC32 H28 F6 N8 O4 ZnP -18.8018; 9.2775; 11.3673
82.433; 68.031; 67.635		796Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
1540035 CIFC40 H44 F6 N8 O4 ZnP 1 21/n 114.5768; 8.9341; 15.9047
90; 103.294; 90		2015.8Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
1540036 CIFC18 H14 F6 N4 O4 ZnP -19.7675; 11.262; 11.576
98.815; 107.953; 112.944		1059.8Nakatake, Daiki; Yokote, Yuki; Matsushima, Yoshimasa; Yazaki, Ryo; Ohshima, Takashi
A highly stable but highly reactive zinc catalyst for transesterification supported by a bis(imidazole) ligand
Green Chem., 2016, 18, 1524
7221876 CIFC19 H11 N O2 SP 1 21/c 112.242; 11.566; 10.526
90; 93.08; 90		1488.2Wan, Jie-Ping; Zhou, Youyi; Liu, Yunyun; Sheng, Shouri
Metal-free oxidative carbonylation on enaminone CC bond for the cascade synthesis of benzothiazole-containing vicinal diketones
Green Chem., 2016, 18, 402
7221978 CIFC4 H6 O4P 1 21/c 110.6016; 9.5305; 10.7702
90; 119.312; 90		948.88Tryznowski, M.; Żołek-Tryznowska, Z.; Świderska, A.; Parzuchowski, P. G.
Synthesis, characterization and reactivity of a six-membered cyclic glycerol carbonate bearing a free hydroxyl group
Green Chem., 2016, 18, 802
7222111 CIFC18 H31 N O4P -19.384; 10.484; 11.281
102.829; 94.191; 113.456		976.4Maleki, Abbas; Nematollahi, Davood; Rasouli, Fereshteh; Zeinodini-Meimand, Azam
Electrode instead of catalyst and enzyme. A greener protocol for the synthesis of new 2-hydroxyacetamide derivatives containing a γ-lactone ring
Green Chem., 2016, 18, 672
7222916 CIFC7 H10 F N O3P 1 21 18.5224; 10.305; 9.1442
90; 90.3404; 90		803.06Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222917 CIFC7 H10 F N O3P 1 21 18.5211; 10.3039; 9.1547
90; 90.365; 90		803.77Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222918 CIFC8 H15 Cl F N O4P -15.821; 6.4875; 15.7485
100.738; 96.625; 94.612		577.23Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222919 CIFC7 H10 F N O3P 1 21/c 112.256; 6.72544; 10.4787
90; 113.193; 90		793.92Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222920 CIFC7 H13 Cl F N O4P 1 21/c 112.235; 11.3068; 7.6415
90; 100.289; 90		1040.12Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7222921 CIFC6 H10 F N O4P -16.5648; 6.6759; 9.6206
98.163; 100.929; 101.047		399.3Willis, Nicky J.; Fisher, Craig A.; Alder, Catherine M.; Harsanyi, Antal; Shukla, Lena; Adams, Joseph P.; Sandford, Graham
Sustainable synthesis of enantiopure fluorolactam derivatives by a selective direct fluorination – amidase strategy
Green Chem., 2016, 18, 1313
7223202 CIFC88 H72 Cd5 N6 O28P 1 21/c 114.6261; 23.2526; 15.7357
90; 107.099; 90		5115.1Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223203 CIFC96 H82 Cd5 N8 O28P 1 21/c 114.5196; 23.367; 15.6042
90; 107.475; 90		5049.8Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223204 CIFC88 H72 Cd3 Cu2 N6 O27P 1 21/c 114.3997; 23.362; 15.543
90; 106.309; 90		5018.4Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223205 CIFC90 H76 Cd5 N6 O28P 1 21/c 114.583; 23.241; 15.6338
90; 106.99; 90		5067.4Qiao, Chengfang; Qu, Xiaoni; Yang, Qi; Wei, Qing; Xie, Gang; Chen, Sanping; Yang, Desuo
Instant high-selectivity Cd-MOF chemosensor for naked-eye detection of Cu(ii) confirmed using in situ microcalorimetry
Green Chem., 2016, 18, 951
7223248 CIFC26 H16 N4 O8 ZnP 1 21/c 119.13; 26.34; 11.628
90; 90.671; 90		5859Gong, Le Le; Feng, Xue Feng; Luo, Feng; Yi, Xian Feng; Zheng, An Min
Removal and safe reuse of highly toxic allyl alcohol using a highly selective photo-sensitive metal‒organic framework
Green Chem., 2016, 18, 2047
7223249 CIFC36 H28 N4 P2P -18.8542; 12.9976; 14.0901
100.076; 90.969; 92.406		1594.63Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
7223250 CIFC40 H34 F6 N4 O6 P2 S2P -114.0858; 14.4866; 15.7112
67.615; 78.55; 62.44		2627Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798
7223251 CIFC38 H33 Cl2 I N4 P2P 1 21/c 19.5438; 39.836; 10.6814
90; 116.464; 90		3635.4Li, Yong-Qi; Wang, Peng; Liu, Huan; Lu, Yong; Zhao, Xiao-Li; Liu, Ye
Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation‒acetalization of olefins
Green Chem., 2016, 18, 1798

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