106575-53-5Relevant articles and documents
A straightforward approach to MMP-2 and MMP-9 inhibitors based on chelate claisen rearrangements
Burkhart, Jens L.,Diehl, Bjoern,Schmitt, Manfred J.,Kazmaier, Uli
experimental part, p. 567 - 575 (2012/03/10)
The chelate Claisen rearrangement is a versatile tool for the stereoselective synthesis of β-substituted γ,δ-unsaturated amino acids, which can be converted into β-substitutedaspartates by oxidative cleavage. These are ideal precursors for the synthesis o
4-Propargyl-2-azetidinone as a versatile synthon for the synthesis of β-lactam antibiotics: Hydrostannation and its reactivities
Nishida,Shibasaki,Ikegami
, p. 1423 - 1433 (2007/10/02)
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