By Gordon W. Gribble and John A. Joule (Eds.)

Development in Heterocyclic Chemistry (PHC), is an annual overview sequence commissioned by means of the foreign Society of Heterocyclic Chemistry (ISHC). Volumes within the sequence include either highlights of the former year's literature on heterocyclic chemistry and articles on new constructing issues of specific curiosity to heterocyclic chemists. The spotlight chapters in quantity 20 are all written through major researchers of their box and those chapters represent a scientific survey of the $64000 unique fabric pronounced within the literature of heterocyclic chemistry in 2007. extra articles during this quantity overview '2-Indolylacyl radicals within the synthesis of indole compounds' and 'Cascade reactions of carbonyl ylides for heterocyclic synthesis'.

Show description

Read or Download A critical review of the 2006 literature preceded by two chapters on current heterocyclic topics PDF

Similar chemistry books

Boiler Water Treatment, Principles and Practice, Vol. 1-2

BOILER WATER remedy, rules AND perform quantity 1 of 2 Volumes through COLIN FRAYNE. Vol. I: Boiler fundamentals and Steam Water Chemistry, ISBN: 0-8206-0371-6 This complete reference is the main useful box consultant ever written on steam and boiler water therapy. during this two-volume instruction manual, Colin Frayne (Cooling Water remedy, rules and perform, additionally by means of Chemical Publishing) analyzes the full spectrum of boiler platforms, together with these utilized in residential complexes, advertisement and institutional structures, and business amenities.

Additional resources for A critical review of the 2006 literature preceded by two chapters on current heterocyclic topics

Example text

Ar---~ . . . - )- Ar--/~ . . . / Ar 9 (mixture (mixtureof of stereoisomers) stereoisomers) 9 Scheme 2 DA Reaction of porphyrin Id ld with a pyrrole-fused 3-sulfolene. Furthermore, it was shown that porphyrin Id ld can also react with a pyrazine o-quinodimethane derivative ( Scheme 3) <05TL2189>. However, in this case the reaction did not afford the expected DA adduct, the product being the porphyrin derivative 10 resulting from the tetradehydrogenation of the corresponding adduct. The porphyrin derivative 11 was also obtained although in minor amount; this product must result from a cyclization reaction between the beta-fused quinoxaline ring and the adjacent meso-aryl group.

112, 35887. P. C. Wren, 1. J. Chern. Chem. , Perkin Trans. 1 1990,2089. 1990, 2089. 42 90TL7021 91 CC877 91CC877 9IJCS(P I) 1733 91JCS(P1)1733 91JMC2477 91J0C5059 91JOC5059 91T8855 91TL4359 92MI1 92MIl 92MIl 92MI1 93JMC2242 94JCS(P 1)1709 94JCS(PI)1709 94MIl 94MI1 94S 142 94S142 94TL2911 95TL4769 97JHCI693 97JHC1693 97T13855 97Tl3855 97TA909 97TL137 98JHCI449 98JHC1449 98JHC499 98JHC983 98JOC6845 98MI1 98MII 98T9995 98TL5731 98TL573I 99AG(E)2419 99BMCL673 99JOM(576) 125 99JOM(576)125 99JPR403 99OL527 990L527 99TL95 00JOCI69 00JOC169 00JOC8086 00JOC8391 00JOC839I 00JOC926 OOSI 00S1 00SL475 01JA3830 0lJA3830 01JNP 100 OIJNPIOO 010L3321 01OL3321 0lSLI878 01SL1878 01T5915 02MI1 02MIl X.

Peyronel, A. Truchon, le. C. Blanchard, A. Doble, O. Piot, lL. L. Zundel, C. Huon, B. Martin, P. Mouton, A. Viroulaud, D. Allam, lJ. Chem. 1991,34,2477. 1991, 34, 2477. Betschart, J. Med. Chern. RJ. L. M. J. L. Barnes, J. Org. Org. Chern. Chem. 1991,56, 1991, 56, 5059. 1991, 47, 8855. M. F. F. Herron, Tetrahedron 1991, H. Shimizu, K. Hamada, M. Ozawa, T. Kataoka, M. Hori, K. Kobayashi, Y. Tada, 1991, 32, 4359. Tetrahedron Lett. 1991,32,4359. Chem. , 117, M. Nakane, K. Satake, K. Ando, H. Wakabayashi, JP 04128276, 1992; 1992; Chern.

Download PDF sample

Rated 4.69 of 5 – based on 25 votes