129768-43-0Relevant articles and documents
Comments on the Asymmetric Synthesis of Chrysogine
Bergman, Jan
, p. 224 - 224 (1997)
The absolute configuration of the mould metabolite chrysogine, (S)-( - )-2-(1-hydroxyethyl)quinazolin-4(3H)-one, was first determined by asymmetric synthesis in 1990 and not in 1996 as recently claimed.
First Asymmetric Synthesis of (S)-(-)-2-(1-Hydroxyethyl)-quinazolin-4(3H)-one (Chrysogenine), a Fungal Metabolite, and Confirmation of the Proposed Absolute Configuration
Maiti, Dilip K.,Ghoshdastidar, Partha Pratim,Bhattacharya, Pranab K.
, p. 306 - 307 (2007/10/03)
Chiral (S)-(-)-2-(1-hydroxyethyl)quinazolin-4(3H)-one (chrysogenine; 7), a fungal metabolite, has been synthesised from anthranilamide and S-(+)-lactic acid, confirming the proposed absolute configuration.