Read e-book online Name Reactions of Functional Group Transformations PDF

By Jie Jack Li, E. J. Corey

ISBN-10: 0471748684

ISBN-13: 9780471748687

This sensible, well-organized reference delves deeply into useful staff modifications, to supply the entire precise info that researchers need.* issues are prepared into the next sections: oxidation, aid, uneven synthesis, and useful team manipulations * each one part encompasses a description of the practical team transformation, the ancient viewpoint, mechanisms, adaptations and enhancements at the response, artificial utilities and purposes for the response, experimental info, and references to the first literature * participants are famous and revered for his or her paintings at the particular identify reactions.

Quality: nice experiment, Searchable, no longer bookmarked

Show description

Read Online or Download Name Reactions of Functional Group Transformations PDF

Similar organic chemistry books

Fereidoon Shahidi's Bailey's Industrial Oil And Fat Products PDF

First released in 1945, Bailey's has develop into the normal reference at the nutrition chemistry and processing know-how on the topic of fit for human consumption oils and the nonedible byproducts derived from oils. This 6th version positive aspects new insurance of fit for human consumption fat and oils and is greater by way of a moment quantity on oils and oilseeds.

Get Organic Farming: Policies and Prospects PDF

Whereas public nervousness approximately genetically engineered foodstuffs and BSE in farm animals has constructed in Europe, at the confident part there was a quickly emerging call for for natural produce. for that reason the natural quarter has moved from a being marginal construction fad to a major topic of coverage situation for politicians and public servants occupied with eu agricultural coverage.

Additional resources for Name Reactions of Functional Group Transformations

Example text

J Org. Chem. 1984, 49,3241-3. [R] Davis, F. -C. Chem. Rev. 1992, 92,919-34. ; Werner, T. Adv. Synth. 2004,346, 143-51, Mimoun, H. Angew. Chem. Inf. Ed Engl. 1982,21,734-50. ; Saussie, L. J. Am. Chem. 1986,108,371 1-8. [R] Sharpless, K. ; Verhoeven, T. R. Aldrichimica Acfa 1979,12,63. [R] Behrens, C. ; Sharpless, K. B. Aldrichimica Acta 1983, 16, 67. Lang, T. ; Wolber, G. J,; Bach, R. D. J. Am. Chem. 1981,103, 3275-82. Bach, R. ; Wolber, G. ; Coddens, B. A. J. Am. Chem. 1984,106*6098-9. ;Troisi, L.

J. Org. Chem. 1984, 49, 1316. Midland, M. ; Gabriel, J. J. Org. Chem. 1989,54, 159. Midland, M. ; Lee, P. E. J. Am. Chem. 1985,107,3237. Brown, J. ; Pai, G. ; Jadhav, P. K. JAm. Chem. 1984, 106,1531. Johnson, W. ; Gopalan, A. S. J. Org. Chem. 1981,46, 1512. ; Kalvin, D. ; Woodard, R. W. Tetrahedron, 1988,44,5597. Ready, M. V. ; Rearick J. ; Rarnachandran, P V. 2001,3, 19. ; Sulikowski, G. A. Org. Lett. 2005, 7, 5163. Julia M. 2 Homogeneous catalytic asymmetric hydrogenation has become one of the most efficient methods for the synthesis of chiral alcohols, amines, a-and p-amino acids, and many other important chiral intermediates.

Reddy, R. ; Carroll, P. J. Org. Chem. 1997,62,2555-63. -C. J. Org. Chem. 1991,56, 1143-5. Richard J. Mullins and Michael T. 1 Description The Midland reduction is the enantioselective reduction of a ketone (1 to an optically active alcohol (2) using the commercially available reagent alpine borane (3). * (+ room temperature 6a ? 0""" 7a 100'C R= n-alkyl Extension of this methodology to an enantioselective variant soon followed. 3 Mechanism and Stereochemical Rationalization Initial debate over the mechanism of the Midland reduction centered around the idea that this reduction could reasonably proceed via either a one-step (Path A) or two-step (Path B) mechanism as shown below.

Download PDF sample

Name Reactions of Functional Group Transformations by Jie Jack Li, E. J. Corey


by Kevin
4.0

Rated 4.63 of 5 – based on 30 votes