Advances in Heterocyclic Chemistry, Vol. 60 by Alan R. Katritzky

April 3, 2017 | Organic | By admin | 0 Comments

By Alan R. Katritzky

The newest quantity within the Advances in Heterocyclic Chemistry sequence

Show description

Read Online or Download Advances in Heterocyclic Chemistry, Vol. 60 PDF

Best organic books

Advances in Heterocyclic Chemistry

(from preface)Volume forty seven of Advances in Heterocyciic Chemistry is, not like such a lot volumes, a monograph and offers with the quantitative points of electro-philic substitution of heterocycles. it really is written by way of Roger Taylor of the college of Sussex, Brighton, England, and your editor with one bankruptcy contributed through Ross Grimmett of the college of Otago in New Zealand.

Chemistry of Heterocyclic Compounds: Thiophene and Its Derivatives, Part Two, Volume 44

Electrophilic Sustitution of Thiophene and Its Derivatives (R. Taylor). Alkylthiophenes and Their Reactions (P. Cagniant, et al. ). Halothiophenes and Their Reactions (M. G. Reinecke & P. Padaja). Nitrothiophenes and Their Reactions (R. ok. Norris). Aminothiophenes and Their Derivatives (R. okay. Norris).

Lewis Base Catalysis in Organic Synthesis, 3 Volume Set

Introductory expense £300 / €399 / $540, legitimate till December 31, 2016, thereafter £340 / €449 / $605This three-volume set represents the 1st entire insurance of the speedily increasing box of Lewis base catalysis that has attracted huge, immense recognition lately. Lewis base catalysis is a conceptually novel paradigm that encompasses a really big variety of preparatively worthwhile changes and is especially potent for enantioselectively developing new stereogenic facilities.

Extra info for Advances in Heterocyclic Chemistry, Vol. 60

Sample text

Wiest, Angew. , Int. Ed. E n g / . 1, 329 (1962). W. R. Carpenter, J. Org. Chem. 27, 2085 (1962). W. P. Norris, J. Urg. Chem. 27, 3248 (1962). G. G. Yakobson, T. D. Petrova, L. I. Kann, T. I. Savchenko, A. K. Petrov, and N. N. , Dokl. Akad. Nauk S S S R 158, 926 (1964) [Dokl. Chem. (Engl. ) 158, 1044 ( 1964)]. A. Logothetis, J. Org. Chem. 29, 3049 (1964). A. A. Gottlieb, Y. Fujita, S. Udenfriend. and B. Witkop, Biochemistry 4, 2507 (1965). J. E. Huheey, J . Phys. Chem. 69, 3284 (1965). H. Suschitzky, Adu.

Org. Chem. 20, 499 ( 1955). E. B. Towne and H. M. S. Pat. 2,726,237 (1955) [CA 50, 6058 (1956)l. R. A. Carboni and R. V. , J. A m . Chem. SOC. 81, 4342 (1959). A. Galbraith, T. Small, and V. Boekelheide, J. Org. Chem. 24, 582 (1959). H. E. Simmons and D. W. Wiley, J. Am. Chem. 82, 2288 (1 960). M. Stacey and J. C. Tatlow, Adu. Fluorine Chem. 1, 166 (1960). A. P. Stefani, L. Herk, and M. Szwarc, J. Am. Chem. 83, 4732 (1961). M. ” Pergamon, Oxford, 1961. J . Sauer and H. Wiest, Angew. , Int. Ed. E n g / .

1, 329 (1962). W. R. Carpenter, J. Org. Chem. 27, 2085 (1962). W. P. Norris, J. Urg. Chem. 27, 3248 (1962). G. G. Yakobson, T. D. Petrova, L. I. Kann, T. I. Savchenko, A. K. Petrov, and N. N. , Dokl. Akad. Nauk S S S R 158, 926 (1964) [Dokl. Chem. (Engl. ) 158, 1044 ( 1964)]. A. Logothetis, J. Org. Chem. 29, 3049 (1964). A. A. Gottlieb, Y. Fujita, S. Udenfriend. and B. Witkop, Biochemistry 4, 2507 (1965). J. E. Huheey, J . Phys. Chem. 69, 3284 (1965). H. Suschitzky, Adu. FIuorine Chem. 4, 1 (1965).

Download PDF sample

Rated 4.53 of 5 – based on 10 votes