As a starting material to prepare (+)- and (−)-homononactic acids, which are used as intermediates in the total synthesis of a cyclic antibiotic tetranactin.[1]
To prepare a chiral phosphorus synthon, which is applicable in the synthesis of phytoprostane B1 type I.[2]
To prepare Eu3+-based precatalysts applicable in the Mukaiyama Aldol reaction in water.[3]
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Manufactured under license by Sterling Pharma Solutions Limited, using Jacobsen HKR technology.
Based on the findings of Nagao et al [1978] that phenacetin is negative in the standard Ames test with Aroclor induced rat S-9 and positive with hamster S-9, the test was performed with a mixture of rat/hamster S-9. Phenacetin was
Journal of cancer research and clinical oncology, 107(3), 149-156 (1984-01-01)
Previous analytical studies of industrial samples of trichloroethylene (TRI) have revealed the presence of mutagenic and carcinogenic epoxides which, it was proposed, might be responsible for the carcinogenicity of such samples, as demonstrated with mice in other laboratories. To test
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