32852-70-3Relevant academic research and scientific papers
Conformational preference and remote (1,10) stereocontrol in biphenyl-2,2′-dicarboxamides
Clayden, Jonathan,Lund, Andrew,Youssef, Latifa H.
, p. 4133 - 4136 (2007/10/03)
(Matrix Presented) The double ortholithiation and electrophilic quench of N,N,N′N′-tetraisopropylbiphenyl-2,2′-dicarboxamide 1 is diastereoselective, giving the chiral C2-symmetric atropisomers of the 3,3′-disubstituted products 3. These chiral
Potential Antitumor Agents. 62. Structure Activity Relationships for Tricyclic Compounds Related to the Colon Tumor Active Drug 9-Oxo-9H-xanthene-4-acetic Acid
Rewcastle, Gordon W.,Atwell, Graham J.,Palmer, Brian D.,Boyd, Peter D. W.,Baguley, Bruce C.,Denny, William A.
, p. 491 - 496 (2007/10/02)
A series of tricyclic analogues of 9-oxo-9H-xanthene-4-acetic acid have been prepared and evaluated for their ability to cause homorrhagic necrosis in subcutaneously implanted colon 38 tumors in mice, in an effort to extend the structure-activity relation
Neutral Ionophores with Selectivity for Na+
Voegtle, Fritz,Kleiner, Thomas,Leppkes, Reinhard,Laeubli, Markus Werner,Ammann, Daniel,Simon, Wilhelm
, p. 2028 - 2034 (2007/10/02)
New non-macrocyclic, electrically neutral ionophores 5 - 9 are described.In membranes they induce selectivities of Na+ over K+ by a factor of up to 20.
