Convergent Synthesis of a Complex Oxime Library Using Chemical Domain Shuffling
摘要:
yThe synthesis of a complex hybrid oxime library is reported utilizing convergent ligation of alkoxyamine and carbonyl monomers via "chemical domain shuffling". Initial biological screening of the library against human small cell lung carcinoma (A549) cells led to the identification of a novel hybrid dimer in contrast to the corresponding monomeric compounds which were found to be inactive.
Diversity-oriented heterocyclic synthesis using divergent reactivity of N-substituted iso(thio)cyanates
作者:Jean-François Vincent-Rocan、Joshua S. Derasp、André M. Beauchemin
DOI:10.1039/c5cc07212c
日期:——
Carbon-substituted isocyanates and isothiocyanates are common building blocks in organic synthesis. In contrast, synthetic uses of N-substituted isocyanates and isothiocyanates are severely underdeveloped: few have been reported and their reactivity...
Remizova,L.A. et al., Journal of Organic Chemistry USSR (English Translation), 1972, vol. 8, p. 1157 - 1160
作者:Remizova,L.A. et al.
DOI:——
日期:——
Synthesis of 5,6,7,8-Tetrahydro-1,6-naphthyridines and Related Heterocycles by Cobalt-Catalyzed [2 + 2 + 2] Cyclizations
作者:Ya Zhou、John A. Porco、John K. Snyder
DOI:10.1021/ol0625280
日期:2007.2.1
Microwave-promoted, cobalt-catalyzed intramolecular [2 + 2 + 2] cyclizations of dialkynylnitriles successfully gave 5,6,7,8-tetrahydro-1,6-naphthyridines. The efficient synthesis of these relatively simple, yet rarely addressed heterocycles enabled the preparation of a collection of these compounds.