Crystallography Open Database
Search results
Result: there are 895 entries in the selection
Switch to the old layout of the pageDownload 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 17
COD ID ![]() |
Links | Formula ![]() |
Space group ![]() |
Cell parameters | Cell volume ![]() |
Bibliography |
---|---|---|---|---|---|---|
1555107 | CIF | C10 H12 O3 | P b c a | 8.8394; 8.5924; 23.437 90; 90; 90 | 1780.1 | Rashid, Showkat; Bhat, Bilal A.; Mehta, Goverdhan Regenerative γ-Lactone Annulations: A Modular, Iterative Approach to Oligo-tetrahydrofuran Molecular Stairs and Related Frameworks. Organic letters, 2015, 17, 3604-3607 |
1519698 | CIF | C10 H13 F O | P 21 21 21 | 5.5342; 11.1421; 14.6505 90; 90; 90 | 903.39 | Witten, Michael R.; Jacobsen, Eric N. A Simple Primary Amine Catalyst for Enantioselective α-Hydroxylations and α-Fluorinations of Branched Aldehydes. Organic letters, 2015, 17, 2772-2775 |
1520307 | CIF | C10 H16 B F2 N O3 | P -1 | 9.5474; 11.4938; 11.5223 92.227; 96.964; 91.605 | 1253.45 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520312 | CIF | C10 H16 B F2 N O4 | I b a 2 | 12.1721; 49.556; 8.341 90; 90; 90 | 5031.3 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
1520313 | CIF | C10 H16 B F2 N O4 | P -1 | 7.0022; 7.7079; 12.3657 83.232; 83.476; 76.265 | 641.26 | Roßbach, Jan; Harms, Klaus; Koert, Ulrich α-Crotyl-α-difluoroboranyloxy-amides: Structure and Reactivity of Isolable Intermediates in Stereospecific α-Ketol Rearrangements. Organic letters, 2015, 17, 3122-3125 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!