Download Chiral Reagents for Asymmetric Synthesis [Handbook of by Leo A. Paquette PDF

By Leo A. Paquette

Derived from the popular, Encyclopedia of Reagents for natural Synthesis (EROS), the comparable editors have created a brand new guide which makes a speciality of chiral reagents utilized in uneven synthesis and is designed for the chemist on the bench. This new instruction manual follows an identical structure because the Encyclopedia, together with an advent and an alphabetical association of the reagents.

As chiral reagents are the foremost for the winning uneven synthesis, selecting the best reagents is vital, during this convenient reference the editors provide information on the best way to organize, shop and use the reagents in addition to delivering key reactions to illustrate the place reagents were effectively used.

  • Comprehensive info on 226 reagents
  • Covers 64 reagents which have been now not incorporated in EROS
  • All info in a single effortless to exploit quantity – at an inexpensive price 

All reagents integrated can be further to e-EROS – please stopover at the location the place you could achieve entry to over 50,000 reactions and 3,800 of the main usually consulted reagents.


Show description

Read or Download Chiral Reagents for Asymmetric Synthesis [Handbook of Reagents for Organic Synthesis] PDF

Best physical chemistry books

Microporous Media Synthesis Properties and Modeling

Featuring new advancements from approximately a decade of development, this reference presents examples of the main unique clinical and technical learn impacting stories in porosity and microporosity—illustrating how you can forecast the houses of microporous buildings for more advantageous digital, building, electric, chemical, army, sanitary, and scientific purposes.

Electroanalytical Chemistry: A Series of Advances, Vol. 22

For greater than 3 many years the Electroanalytical Chemistry sequence has introduced the main in-depth and important examine relating to matters in electrochemistry.  quantity 22 maintains this gold-standard with functional reports of modern purposes, in addition to cutting edge contributions from the world over revered specialists—highlighting the emergence of recent applied sciences and traits within the box.

Free Energy Relationships in Organic and Bio-Organic Chemistry

Introducing the applying of loose strength correlations to elucidating the mechanisms of natural and bio-organic reactions, this publication offers a brand new and illuminating approach of drawing close a in all probability advanced subject. the belief of the way loose strength correlations derive from polar substituent swap is brought, and customary pitfalls encountered within the program of unfastened strength relationships are defined, in addition to using those anomalies in mechanistic reports.

Extra info for Chiral Reagents for Asymmetric Synthesis [Handbook of Reagents for Organic Synthesis]

Example text

Chem. Soc. 1981, 103, 6967. ; Manners, A. Tetrahedron Lett. 1988,29, 4481. ; Groth, U. ; Schollkopf, U. J. Am. Chem. Soc. ; Dyker, H. LiebigsAnn. Chem. 1990,1107. ; Mundinger, K. Tetrahedron Lett. 1988, 29, 1269. (f) Hauck, R. ; Fuhrhop, J. ; Nau, H. Life ScL 1990, 46, 513. ; Ripa, A. HeIv. Chim. Acta 1992, 75, 2657. J. ; Eichenauer, H. Angew. Chem. 1979, 91, 425; Angew. , Int. Ed. Engl. 1979, 18, 397. ; Tokoroyama, T. Chem. Commun. 1987,358. (c)Pennanen, S. I. Acta. Chem. Scand. 1981, B35, 555.

C ; Preston, S. C ; Sutton, K. ; Walker, J. C. Bull Soc. Chem. Fr. 1987, 608. 2. Bibler, J. ; Wojcicki, A. Inorg. Chem. 1966, 5, 889. 3. ; Schmidt, E. / Organomet. Chem. 1972, 36, C18. ; Schmidt, E. J. Organomet. Chem. 1973, 50, 219. ; Strutz, J. , Teil B 1974, 29, 446. 4. ; Davies, S. ; Felkin, H. Chem. Commun. 1982, 1303. 5. Liebeskind, L. ; Welker, M. E. /. Organomet. Chem. 1983, 2, 194. 6. (a) Davies, S. ; Dordor-Hedgecock, I. ; Sutton, K. ; Walker, J. C ; Bourne, C ; Jones, R. ; Prout, K. Chem.

1990, 31, 1213. ; Schafer, T. ; Bhushan, V. Tetrahedron Lett. 1988, 29, 2437. ; Nakai, S. HeIv. Chim. Acta 1990, 73, 1833. ; Nakai, S. Chem. Ber. 1991, 124, 219. ; Raabe, G. Synlett 1992, 897. 11. ; Tom Dieck, H. Z. Anorg. AlIg. Chem. 1988, 560, 80. 12. ; Dorrity, M. J. ; Malone, J. ; Norbert, W. D. J. ; Sridharan, V. Tetrahedron Lett. 1990, 31, 3075. 13. Hwu, J. ; Wang, N. Tetrahedron 1988, 44, 4181. 14. ; Fourrey, J. ; Das, B. C. Tetrahedron Lett. 1988, 29, 4423. ; Das, B. C , Synlett 1992, 431.

Download PDF sample

Rated 4.91 of 5 – based on 44 votes