Automation in the organic chemistry laboratory: Why? How?

Articles in the same Issue

1. New reactions for use in natural products chemistry
2. Synthetic studies in the mevinoid field. The total synthesis of ML236A
3. Synthesis design logic and the SYNGEN (synthesis generation) program
4. Computer assistance in the design of syntheses and a new generation of computer programs for the solution of chemical problems by molecular logic
5. Asymmetric synthesis and its applications: towards the synthesis of bryostatin 1
6. Enantioselective alkylation of carbonyl compounds. From stoichiometric to catalytic asymmetric induction
7. Asymmetric C-C bond formation using organometallic chemistry
8. Transition metal templates as guides for cycloadditions
9. Superbases for organic synthesis
10. Captodative substituent effects in radical chemistry
11. Synthetic methodology involving radical cyclization: spiro compounds and α-oxo radicals
12. Stereoselective syntheses with carbohydrate radicals
13. Lactone synthesis by electron transfer and radical chemistry
14. Automation in the organic chemistry laboratory: Why? How?
15. Stereocontrolled reactions through heterocyclic intermediates
16. Asymmetric synthesis via nor-ephedrine derived 2-alkenyloxazolidines
17. Recent results in the field of asymmetric synthesis using chiral sulfoxides
18. New synthetic applications of dialkylboron halide reagents
19. New, useful reactions of novel haloformates and related reagents
20. Organic chemistry with lanthanides