Crystallography Open Database

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1506498 CIFC23 H20 N2 O8P -18.245; 9.07; 15.501
93.34; 91.41; 110.26		1084.4Lu, Chong-Dao; Liu, Hui; Chen, Zhi-Yong; Hu, Wen-Hao; Mi, Ai-Qiao
Three-component reaction of aryl diazoacetates, alcohols, and aldehydes (or imines): evidence of alcoholic oxonium ylide intermediates.
Organic letters, 2005, 7, 83-86
1506499 CIFC30 H28 N2 O7P -19.058; 10.3496; 14.987
74.357; 78.955; 86.161		1327.7Lu, Chong-Dao; Liu, Hui; Chen, Zhi-Yong; Hu, Wen-Hao; Mi, Ai-Qiao
Three-component reaction of aryl diazoacetates, alcohols, and aldehydes (or imines): evidence of alcoholic oxonium ylide intermediates.
Organic letters, 2005, 7, 83-86
1506500 CIFC17 H17 Br O3P 21 21 2112.425; 21.493; 5.9427
90; 90; 90		1587Itoh, Kennosuke; Hasegawa, Masayuki; Tanaka, Junji; Kanemasa, Shuji
Enantioselective enol lactone synthesis under double catalytic conditions.
Organic letters, 2005, 7, 979-981
1506501 CIFC38 H40 N3 O6P -111.852; 15.102; 19.607
74.327; 86.668; 73.37		3237Oguri, Hiroki; Schreiber, Stuart L.
Skeletal diversity via a folding pathway: synthesis of indole alkaloid-like skeletons.
Organic letters, 2005, 7, 47-50
1506502 CIFC43 H47 N7 O10 SP 1 21/n 115.165; 11.97; 22.819
90; 92.248; 90		4139Oguri, Hiroki; Schreiber, Stuart L.
Skeletal diversity via a folding pathway: synthesis of indole alkaloid-like skeletons.
Organic letters, 2005, 7, 47-50

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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.