Coupling reaction of chalcogenyl halides with alkynes on a solid support. Synthesis of new selenium-containing retinoids

Gendre, Fabrice; Diaz, Philippe

doi:10.1016/s0040-4039(00)00761-9

Cited by 6 publications

(2 citation statements)

References 15 publications

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“…The total number of libraries cited was 284, comparable to the 297 figure for 1999, bringing the cumulative total to over 1250 libraries published since 1992 − …”

mentioning

confidence: 80%

Comprehensive Survey of Combinatorial Library Synthesis: 2000

Dolle

2001

J. Comb. Chem.

197

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An exhaustive compilation of biologically active libraries covering the years 1992-1997 was presented in a previous review [1a]. In that review, libraries were divided among 4 major categories, including those active against proteases, non-proteolytic enzymes, Gprotein coupled receptors, and non-G-protein coupled receptors. A generic structure for each library was provided as well as the structure of the most active member. The number of biologically active libraries reported in the literature during this time period (86 total) represents <25% of the total number of published library constructs. Disclosure of library synthesis without accompanying screening data is a more common occurrence. Because these types of libraries are equally important to the practicing combinatorial chemist, it was thought that a comprehensive listing of such libraries spanning the years 1992-1997 would be a useful supplement to the previous review [1a,b].Library constructs [2-248] listed herein are relegated to one of five tables. Table 1 is entitled 'Scaffold derivatization' and includes all constructs in which a multi-functional scaffold is modified in some fashion to create a library. An example of a construct found in Table 1 would be the sequential addition of three nucleophiles to trichloropyrimidine. Table 2, entitled 'Acyclic synthesis', lists all linear constructs such as those derived from multi-component Ugi condensations.

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