Crystallography Open Database

Result: there are 788 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 'Organic Letters' volume of publication is 15

Blue left arrow Blue left arrow First | Blue left arrow Previous 5 | of 158 | Next 5 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
1508861 CIFC34 H32 N4P 1 21/c 113.046; 18.896; 21.809
90; 91.007; 90		5375Chandra, Brijesh; Mahanta, Sanjeev P.; Pati, Narendra N.; Baskaran, Sambath; Kanaparthi, Ravi K.; Sivasankar, Chinnappan; Panda, Pradeepta K.
Calix[2]bispyrrolylarenes: New Expanded Calix[4]pyrroles for Fluorometric Sensing of Anions via Extended π-Conjugation.
Organic letters, 2013, 15, 306-309
1508862 CIFC24 H16 N2P 1 21 17.6144; 7.5543; 29.9948
90; 91.624; 90		1724.65Louillat, Marie-Laure; Patureau, Frederic W.
Toward polynuclear ru-cu catalytic dehydrogenative C-N bond formation, on the reactivity of carbazoles.
Organic letters, 2013, 15, 164-167
1508863 CIFC24 H24 O4P -19.2295; 10.3951; 11.3783
86.591; 69.851; 79.622		1008.07Qin, Changming; Davies, Huw M. L.
Enantioselective Synthesis of 2-Arylbicyclo[1.1.0]butane Carboxylates.
Organic letters, 2013, 15, 310-313
1508864 CIFC25 H25 N3 O3C 1 2 121.033; 9.9868; 10.2026
90; 102.928; 90		2088.8Hong, Bor-Cherng; Liao, Wei-Kai; Dange, Nitin S.; Liao, Ju-Hsiou
One-pot organocatalytic enantioselective domino double-Michael reaction and pictet-spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers.
Organic letters, 2013, 15, 468-471
1508865 CIFC25 H24 Cl N3 O3P 21 21 218.1146; 9.2164; 35.493
90; 90; 90		2654.4Hong, Bor-Cherng; Liao, Wei-Kai; Dange, Nitin S.; Liao, Ju-Hsiou
One-pot organocatalytic enantioselective domino double-Michael reaction and pictet-spengler-lactamization reaction. A facile entry to the "inside yohimbane" system with five contiguous stereogenic centers.
Organic letters, 2013, 15, 468-471

Blue left arrow Blue left arrow First | Blue left arrow Previous 5 | of 158 | Next 5 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!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.