Crystallography Open Database

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Searching year of publication is 2013

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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
1508866 CIFC12 H18 F6 N2 O2P 1 2/c 19.4219; 8.6467; 18.7345
90; 103.222; 90		1485.81Riofski, Mark V.; Hart, Allison D.; Colby, David A.
Amidinate salt of hexafluoroacetone hydrate for the preparation of fluorinated compounds by the release of trifluoroacetate.
Organic letters, 2013, 15, 208-211
1508867 CIFC25 H28 Cl N O6P 1 21/n 113.871; 11.664; 15.1202
90; 92.72; 90		2443.6Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L.
Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.
Organic letters, 2013, 15, 350-353
1508868 CIFC29 H29 N O6P 1 21/c 19.4038; 10.7199; 24.4225
90; 99.093; 90		2431.04Gorbacheva, Evgenia O.; Tabolin, Andrey A.; Novikov, Roman A.; Khomutova, Yulia A.; Nelyubina, Yulia V.; Tomilov, Yury V.; Ioffe, Sema L.
Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.
Organic letters, 2013, 15, 350-353

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