19255-60-8Relevant academic research and scientific papers
Organocatalyzed Michael-Henry reactions: Enantioselective synthesis of cyclopentanecarbaldehydes via the dienamine organocatalysis of a succinaldehyde surrogate
Hong, Bor-Cherng,Chen, Po-Yuan,Kotame, Prakash,Lu, Pei-Ying,Lee, Gene-Hsiang,Liao, Ju-Hsiou
supporting information; experimental part, p. 7790 - 7792 (2012/09/22)
Asymmetric formal [3+2] cycloadditions of 4-hydroxybut-2-enal, a succinaldehyde surrogate, and nitroalkenes with an organocatalyst provided cyclopentanecarbaldehydes containing four consecutive stereogenic centers with excellent enantioselectivities.
HEMATOPOIETIC NEOPLASM CHEMOTHERAPY
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, (2010/11/03)
A method and medicament for treating mixed lineage leukemia; translocated mixed lineage leukemia; translocated mixed lineage leukemia based acute myelogenous leukemia; translocated mixed lineage leukemia based acute lymphoid leukemia; a non-MLL based chronic myeloproliferative disorder, or non-MLL based acute lymphoid leukemia is provided.
IMIDAZOPYRIDAZINES FOR USE AS PROTEIN KINASE INHIBITORS
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Page/Page column 139-140, (2009/06/27)
There is provided compounds of formula (I): wherein Z, M, R1, X, R3, R4 and R5 have meanings given in the description, an pharmaceutically-acceptable esters, amides, solvates or salts thereof, which compounds are useful in the treatment of diseases in which inhibition of a protei kinase (e.g. a PIM family kinase or PI3-K) is desired and/or required, an particularly in the treatment of cancer.
Stereoselective synthesis of methyl and ethyl (2E,4Z)-2,4-decadienoates from (E)-4,4-dimethoxy-2-butenal
Ovanesyan,Garibyan,Badanyan
, p. 951 - 954 (2007/10/03)
Methyl and ethyl (2E,4Z)-2,4-decadienoates were synthesized starting from (E)-4,4-dimethoxy-2-butenal.
SYNTHESE STEREOSELECTIVE DU DECADIENE-2(E), 4(Z)OATE D'ETHYLE. A PARTIR D'UN MONOACETAL DU GLYOXAL
Stambouli, A.,Amouroux, R.,Chastrette, M.
, p. 5301 - 5302 (2007/10/02)
The glyoxal monoacetal 2, now readily available in bulk quantity, is a very useful synthon for the dienes-1,3 synthesis, as illustrated in the stereoselective preparation of ethyl 2E,4Z-decadienoate using two Wittig-type olefination reactions.
