Crystallography Open Database

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Searching journal of publication like 'The Journal of organic chemistry' volume of publication is 80

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4036387 CIFC24 H24 O4P 21 21 219.872; 12.077; 16.125
90; 90; 90
1922.5Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036388 CIFC52 H56 O12P b c a7.968; 20.772; 26.086
90; 90; 90
4318Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036389 CIFC24 H36 O4P 1 21/n 112.61; 10.614; 15.843
90; 95.485; 90
2110.8Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036390 CIFC24 H24 O4P -17.992; 9.923; 12.384
82.119; 86.351; 83.885
966.1Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036391 CIFC26 H28 O4P -18.018; 9.654; 14.715
81.337; 80.762; 69.641
1048.5Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036392 CIFC20 H19 N O4P 1 21/n 116.482; 9.0409; 22.9016
90; 106.472; 90
3272.6Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036393 CIFC42 H55 O6P 21 21 2112.5302; 13.0867; 22.9933
90; 90; 90
3770.4Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036394 CIFC42 H54 F2 O6P 1 21 114.06; 9.757; 15.785
90; 96.018; 90
2153.5Ghorai, Manas K.; Halder, Sandipan; Das, Subhomoy
Domino Michael-Michael and Aldol-Aldol Reactions: Diastereoselective Synthesis of Functionalized Cyclohexanone Derivatives Containing Quaternary Carbon Center.
The Journal of organic chemistry, 2015, 80, 9700-9712
4036395 CIFC17 H13 N OP 21 21 215.5809; 14.442; 16.1693
90; 90; 90
1303.24Chinta, Bhavani Shankar; Baire, Beeraiah
Stereoselective, Cascade Synthesis of trans-Enynones through Coupling-Isomerization Reaction.
The Journal of organic chemistry, 2015, 80, 10208-10217
4036396 CIFC16 H14 O2P b c a11.97; 7.4348; 29.213
90; 90; 90
2599.8Chinta, Bhavani Shankar; Baire, Beeraiah
Stereoselective, Cascade Synthesis of trans-Enynones through Coupling-Isomerization Reaction.
The Journal of organic chemistry, 2015, 80, 10208-10217
4036397 CIFC25 H18 O2C 1 2/c 143.875; 8.776; 19.789
90; 98.921; 90
7528Yuan, Zhenbo; Fang, Xinxin; Li, Xuanyi; Wu, Jie; Yao, Hequan; Lin, Aijun
1,6-Conjugated Addition-Mediated [2+1] Annulation: Approach to Spiro[2.5]octa-4,7-dien-6-one.
The Journal of organic chemistry, 2015, 80, 11123-11130
4036398 CIFC29 H32 O2P 1 21/c 113.417; 19.553; 9.7821
90; 108.595; 90
2432.3Yuan, Zhenbo; Fang, Xinxin; Li, Xuanyi; Wu, Jie; Yao, Hequan; Lin, Aijun
1,6-Conjugated Addition-Mediated [2+1] Annulation: Approach to Spiro[2.5]octa-4,7-dien-6-one.
The Journal of organic chemistry, 2015, 80, 11123-11130
4036399 CIFC54 H54 N8 O12 S2P -113.239; 15.838; 17.467
90.102; 106.346; 112.778
3214.9Zhao, Hong-Wu; Tian, Ting; Li, Bo; Yang, Zhao; Pang, Hai-Liang; Meng, Wei; Song, Xiu-Qing; Chen, Xiao-Qin
Diastereoselective Synthesis of Dispirobarbiturates through Et3N-Catalyzed [3 + 2] Cycloaddition of Barbiturate-Based Olefins with 3-Isothiocyanato Oxindoles.
The Journal of organic chemistry, 2015, 80, 10380-10385
4036400 CIFC24 H22 N4 O5 SP 1 21/c 116.284; 7.5128; 19.09
90; 108.77; 90
2211.2Zhao, Hong-Wu; Tian, Ting; Li, Bo; Yang, Zhao; Pang, Hai-Liang; Meng, Wei; Song, Xiu-Qing; Chen, Xiao-Qin
Diastereoselective Synthesis of Dispirobarbiturates through Et3N-Catalyzed [3 + 2] Cycloaddition of Barbiturate-Based Olefins with 3-Isothiocyanato Oxindoles.
The Journal of organic chemistry, 2015, 80, 10380-10385
4036401 CIFC27.5 H30.5 Cl1.5 N2 O3P 21 21 219.96; 18.65; 28.449
90; 90; 90
5284.5Attaba, Nassilia; Taylor, James E.; Slawin, Alexandra M. Z.; Smith, Andrew D.
Enantioselective NHC-Catalyzed Redox [4 + 2]-Hetero-Diels-Alder Reactions Using α,β-Unsaturated Trichloromethyl Ketones as Amide Equivalents.
The Journal of organic chemistry, 2015, 80, 9728-9739
4036402 CIFC5 H6 Cl N O4 S2P 1 21/c 15.0223; 11.561; 16.488
90; 96.509; 90
951.2Barany, George; Britton, Doyle; Chen, Lin; Hammer, Robert P.; Henley, Matthew J.; Schrader, Alex M.; Young, Jr, Victor G
Unexpectedly Stable (Chlorocarbonyl)(N-ethoxycarbonylcarbamoyl)disulfane, and Related Compounds That Model the Zumach-Weiss-Kühle (ZWK) Reaction for Synthesis of 1,2,4-Dithiazolidine-3,5-diones.
The Journal of organic chemistry, 2015, 80, 11313-11321
4036403 CIFC14 H18 N2 O4 S2C 1 2/c 119.338; 9.106; 21.687
90; 118.47; 90
3357Barany, George; Britton, Doyle; Chen, Lin; Hammer, Robert P.; Henley, Matthew J.; Schrader, Alex M.; Young, Jr, Victor G
Unexpectedly Stable (Chlorocarbonyl)(N-ethoxycarbonylcarbamoyl)disulfane, and Related Compounds That Model the Zumach-Weiss-Kühle (ZWK) Reaction for Synthesis of 1,2,4-Dithiazolidine-3,5-diones.
The Journal of organic chemistry, 2015, 80, 11313-11321
4036404 CIFC6 H9 N O5 S2P 1 21/c 14.862; 11.891; 17.893
90; 93.661; 90
1032.4Barany, George; Britton, Doyle; Chen, Lin; Hammer, Robert P.; Henley, Matthew J.; Schrader, Alex M.; Young, Jr, Victor G
Unexpectedly Stable (Chlorocarbonyl)(N-ethoxycarbonylcarbamoyl)disulfane, and Related Compounds That Model the Zumach-Weiss-Kühle (ZWK) Reaction for Synthesis of 1,2,4-Dithiazolidine-3,5-diones.
The Journal of organic chemistry, 2015, 80, 11313-11321
4036405 CIFC12 H14 N2 O4 S2P -17.2854; 8.4243; 12.9967
100.849; 94.925; 113.418
707.36Barany, George; Britton, Doyle; Chen, Lin; Hammer, Robert P.; Henley, Matthew J.; Schrader, Alex M.; Young, Jr, Victor G
Unexpectedly Stable (Chlorocarbonyl)(N-ethoxycarbonylcarbamoyl)disulfane, and Related Compounds That Model the Zumach-Weiss-Kühle (ZWK) Reaction for Synthesis of 1,2,4-Dithiazolidine-3,5-diones.
The Journal of organic chemistry, 2015, 80, 11313-11321
4036406 CIFC20 H15 Br F3 N O3C 1 2 122.1075; 7.7997; 22.3762
90; 92.119; 90
3855.7Zhao, Mei-Xin; Zhu, Hui-Kai; Dai, Tong-Lei; Shi, Min
Cinchona Alkaloid Squaramide-Catalyzed Asymmetric Michael Addition of α-Aryl Isocyanoacetates to β-Trifluoromethylated Enones and Its Applications in the Synthesis of Chiral β-Trifluoromethylated Pyrrolines.
The Journal of organic chemistry, 2015, 80, 11330-11338

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