2017
DOI: 10.1016/j.tetlet.2017.03.034
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Enantioselective rhodium-catalyzed hydroacylation to access the four stereoisomers of anti-rodent difenacoum

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Cited by 4 publications
(1 citation statement)
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“…In 1975, DIF was developed amidst increasing concern about warfarin-resistant rats [ 3 ]. The anticoagulant activity of DIF is more effective and toxic than the first-generation anticoagulant rodenticides, such as warfarin, because of the introduction of substituted tetralinyl on the side chain [ 4 , 5 ]. DIF can act as an anti-vitamin K anticoagulant to block the vitamin K cycle, which stops the activity of the vitamin K-dependent clotting factor and impairs the biosynthesis of a variety of coagulation functions [ 6 ].…”
Section: Introductionmentioning
confidence: 99%
“…In 1975, DIF was developed amidst increasing concern about warfarin-resistant rats [ 3 ]. The anticoagulant activity of DIF is more effective and toxic than the first-generation anticoagulant rodenticides, such as warfarin, because of the introduction of substituted tetralinyl on the side chain [ 4 , 5 ]. DIF can act as an anti-vitamin K anticoagulant to block the vitamin K cycle, which stops the activity of the vitamin K-dependent clotting factor and impairs the biosynthesis of a variety of coagulation functions [ 6 ].…”
Section: Introductionmentioning
confidence: 99%