By Milos Hudlicky
Presents entire insurance of the categories of savings passed through by means of many of the periods of natural chemistry. Discusses discounts in response to what bond or useful workforce is lowered by means of assorted reagents. supplies detailed cognizance to selective discounts which are appropriate for the aid of 1 specific kind of bond or functionality with out affecting different bonds or features found in a similar molecule. exact emphasis is put on enantioselective and diastereoselective mark downs effected either by way of chiral reagents and by means of microorganisms. lowering brokers are correlated with either the beginning compounds and the goods of relief. contains discussions of tools, mechanisms, stereochemistry, and scopes of lowering brokers. chosen laboratory approaches exhibit the most aid options. Correlation tables and thorough writer and topic indexes make this booklet effortless to exploit.
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Extra info for Reductions in Organic Chemistry
11–14]); we are not going to discuss them here in any detail. All of them (including, of course, CECA itself) are a posteriori means of analysis, that is, they can be applied after a conventional ab initio SCF calculation has been performed, in order to elucidate the results of the latter. The aim of the present paper is to use the same integral approximation scheme in order to develop an approximate ab initio scheme of a priori calculations, in which one needs not to calculate any three- and four-center integrals.
Mezey PG (1982) Int J Quant Chem 22:101–114 8. Mezey PG (1982) Chem Phys Lett 87:277–279 9. Mezey PG (1983) Int J Quant Chem 24:523–526 10. Mezey PG (1984) Can J Chem 62:1356–1357 11. Mezey PG (1984) J Chem Phys 80:5055–5057 12. Mezey PG (1985) J Am Chem Soc 107:3100–3105 13. Mezey PG (1985) Surf Sci 156:597–604 14. Mezey PG (1986) Int J Quant Chem 29:85–99 15. Mezey PG (1986) Int J Quant Chem 29:333–343 16. Otto P, Ladik J, Mezey PG (1987) J Math Chem 1:85–96 17. Cassam-Chenaï P, Chiaramello J-M, Mezey PG (2008) J Math Chem 44:981–987 18.
Otto P, Ladik J, Mezey PG (1987) J Math Chem 1:85–96 17. Cassam-Chenaï P, Chiaramello J-M, Mezey PG (2008) J Math Chem 44:981–987 18. Mezey PG (2007) AIP Conf Proc 963:513–516 19. Mezey PG (2012) AIP Conf Proc 1504:725–728 20. Mezey PG (2015) J Phys Chem A 119:5305–5312 21. Mezey PG (2015) Topological tools for the study of families of reaction mechanisms: the fundamental groups of potential surfaces in the universal molecule context. In: Alikhani E, Chauvin R, Lepetit C, Silvi B (eds) Applications of topological methods in molecular chemistry.