474642-05-2Relevant academic research and scientific papers
IMPROVEMENTS IN OR RELATING TO ORGANIC COMPOUNDS
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Page/Page column 8, (2021/04/10)
The use of compounds according to formula (I) and with X, Y = –NH– or –O–, wherein at least X or Y is –NH–, in the form of any one of its stereoisomers or a mixture thereof, wherein is indicating a carbon-carbon single or double bond, and wherein one carbon-carbon double bond is present either at C2 or C3, the wavy bond is indicating an unspecified configuration of the adjacent double bond, as umami tastant.
Total synthesis of (+)-grandiamide D, dasyclamide and gigantamide A from a Baylis-Hillman adduct: A unified biomimetic approach
Ilangovan, Andivelu,Saravanakumar, Shanmugasundar
supporting information, p. 127 - 133 (2014/02/14)
A unified strategy was followed for the synthesis of three putrescine bisamides, (+)-grandiamide D, dasyclamide and gigantamide A, isolated from leaves of Aglaia gigantea, by making use of a common synthetic intermediate prepared by the Baylis-Hillman rea
Synthesis and structure elucidation of open-chained putrescine-bisamides from Aglaia species
Detterbeck, Richard,Hesse, Manfred
, p. 6887 - 6893 (2007/10/03)
The structures of the eight recently described open-chained putrescine bisamide alkaloids secoodorine (1), aglaithioduline (3), aglaiduline (4), aglaidithioduline (5), grandiamide B (13), grandiamide C (14), pyramidatine (20), and secopiriferine (22), which were isolated from different Aglaia species, have been verified by synthesis. In addition to that, the published structure 2 for hemileptagline had to be revised, and for secoodorine (1) the absolute configuration could be established.
