Enzymes in Action: Green Solutions for Chemical Problems by Ulrike T. Strauss, Kurt Faber (auth.), Binne Zwanenburg,

By Ulrike T. Strauss, Kurt Faber (auth.), Binne Zwanenburg, Marian Mikołajczyk, Piotr Kiełbasiński (eds.)

Enzymes in Action is a well timed survey of a latest improvement in natural chemistry. it really is transparent that bioreagents call for that natural chemists imagine otherwise. in the event that they accomplish that, they'll open up new avenues of intriguing, new chemistry that might allow difficulties to be solved in a chic manner.
the 1st part covers the thoughts essential to comprehend enzymes in molecular operations. the second one part covers heteroatom enzyme chemistry, with enormous awareness being given to using enzymes within the cleansing of chemical war brokers and their software in environmental difficulties. the ultimate part highlights the strategic use of enzymes in natural chemistry.
it really is transparent that the time period `green chemistry' is suitable, on the grounds that enzyme mediated strategies ensue below light, environmentally benign stipulations, and enzymes allow chemists to accomplish new chemical operations that may rather be tricky to accomplish at all.

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Enzymes in Action: Green Solutions for Chemical Problems Proceedings of the NATO Advanced Study Institute on Enzymes in Heteroatom Chemistry (Green Solutions for Chemical Problems) Berg en Dal, The Netherlands 19–30 June 1999

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Additional info for Enzymes in Action: Green Solutions for Chemical Problems Proceedings of the NATO Advanced Study Institute on Enzymes in Heteroatom Chemistry (Green Solutions for Chemical Problems) Berg en Dal, The Netherlands 19–30 June 1999

Example text

However, the rules in Figure 3 cannot account for changes in selectivity that may be caused by small changes in the structure of the secondary alcohol. 6) under the same conditions [10], Figure 4. Both an ethyl and a -CH2Br group have similar sizes, so the difference suggests that polar character of the bromine lowers the enantioselectivity. Similarly, changing the position of a methyl substituent in the aryl ring of the large substituent drastically altered the selectivity of PCL from E > 1()() in the para-substituted isomer to E =27 in the ortho-substituted isomer [11].

Unfortunately, however, frequently myo-inositol phosphates are only accessible in minute amounts from scarce natural sources after laborious isolation and purification procedures. Clearly, the elucidation of their biological role would be greatly facilitated if these molecules could be made available via facile synthetic routes. Therefore, we explored new synthetic routes toward these molecules using enzymes for the introduction of chirality into the respective molecular backbone. myo-Inositol itself, derived from ubiquitous and abundantly available phytic acid, is by far the most conveniently accessible and economical starting material.

1997) in Ed. , Ester Synthesis via Acyltransfer (Transesterification), Methods in Enzymology, Vol. 286, chapter 19, Academic Press, 406 -443. 2. Laumen, K. (1987) Ph. D. P. (1992) Pure Appl. Chem. P. (1993) Indian J. Chem. Sec B 328,145. 3. P. (1993) J. Chromatogr. 633, 287. 4. P. (1993) Tetrahedron: Asymmetry 4, 1017. 5. Haase, B. (1997) Ph. D. thesis, Wuppertal. 6. , Masuda, S. , Masuda, S. (1979) Tetrahedron 35,1601. 7. S. (1974) Tetrahedron Lett. K. (1979) Synth. Commun. 9, 431. 8. B. F. (1990) Methods in Inosite Research Raven Press New York.

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