157639-01-5Relevant articles and documents
New DNA binding ligands as a model of chromomycin A3
Imoto, Shuhei,Haruta, Yoshinari,Watanabe, Kyouichi,Sasaki, Shigeki
, p. 4855 - 4859 (2007/10/03)
Small molecules with DNA-binding affinity within the minor groove have become of great interest. In this study, new DNA-binding ligands were designed to mimic Chromomycin A3 (CRA3), which contains a hydroxylated tetrahydroanthracene
Synthesis of termini-differentiated 6-carbon stereotetrads: An alkylative oxidation strategy for preparation of the C21-C26 segment of apoptolidin
Chen, Yuzhong,Evarts Jr., Jerry B.,Torres, Eduardo,Fuchs, Philip L.
, p. 3571 - 3574 (2007/10/03)
(graph presented) Two methods have been developed for the synthesis of epoxide 36. The first uses (+)-pulegone 25 as an enantiopure starting material and introduces the requisite intricacy of target 22 in 12 operations. The second method employs an enanti
Enantiodivergent syntheses of (R)- and (S)- 3,5-dimethylcyclohex-2-en-1- ones from (R)-pulegone
Nangia,Prasuna
, p. 1989 - 1998 (2007/10/02)
R-(+)-pulegone (1) is transformed to (R)-5-methyl-2- (phenylsulfinyl)cyclohexanone (5) (65%, 3 steps). Sulfoxide 5 is converted to R-(-)-3,5-dimethylcyclohex-2-en-1-one (4) (53%, 4 steps) and S-(+)-4 (26%, 3 steps).