3975-91-5Relevant academic research and scientific papers
Matlystatins, new inhibitors of type IV collagenases from Actinomadura atramentaria. IV. Synthesis and structure-activity relationships of matlystatin B and its stereoisomers
Tamaki,Kurihara,Oikawa,Tanzawa,Sugimura
, p. 1481 - 1492 (2007/10/02)
The first total synthesis of matlystatin B (1a), a low molecular weight inhibitor of type IV collagenases, was accomplished, and its absolute configuration was unambiguously determined. Furthermore, ten stereoisomers of 1a were synthesized, and the inhibi
Synthesis and determination of the absolute configuration of matlystatin B
Tamaki,Ogita,Tanzawa,Sugimura
, p. 683 - 686 (2007/10/02)
The title compound (1) was first synthesized and its absolute configuration was determined as shown in figure 1.
ASYMMETRIC INDUCTION IN THE CYCLOADDITION REACTION OF DICHLOROKETENE WITH CHIRAL ENOL ETHERS. A VERSATILE APPROACH TO OPTICALLY ACTIVE CYCLOPENTENONE DERIVATIVES.
Greene, Andrew E.,Charbonnier, Florence
, p. 5525 - 5528 (2007/10/02)
Significant asymmetric induction has been observed in the cycloaddition reaction of dichloroketene with chiral enol ethers.The resultant diastereomeric cyclobutanones have been converted to synthetically useful α-chlorocyclopentenones in optically active form.
