A Critical Review of the 2004 Literature Preceded by Two by Gribble Prof , Gordon Gribble , John Joule Prof Gribble

By Gribble Prof , Gordon Gribble , John Joule Prof Gribble Prof

This can be the 17th annual quantity of growth in Heterocyclic Chemistry, which covers the literature released in the course of 2004 on lots of the vital heterocyclic ring structures. the amount opens with really expert studies: Dennis Wright covers Furans as flexible Synthons for Target-Oriented and Diversity-Oriented Synthesis; and John Hepworth and Mark Heron speak about 'The Synthesis and Photochromic homes of Naphthopyrans'. the rest chapters study the hot literature at the universal heterocycles so as of accelerating ring dimension and the heteroatoms current. * comprises new contributions from specialists within the box* Covers literature released in the course of 2004 on many of the very important heterocyclic ring platforms * provides reports on flexible Synthons for Target-Oriented and Diversity-Oriented Synthesis; and Synthesis and Photochromic homes of Naphthopyrans

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Acharya, Tetrahedron Lett. 2001, 42, 2817. 01TL3603 A. Yoshida, H. Takayama, Tetrahedron Lett. 2001, 42, 3603. J. B. A. S. Walter, Tetrahedron Lett. 2001, 42, 5841. 01TL7041 O. Arjona, G. Lorenzo, R. Medel, J. Plumet, Tetrahedron Lett. 2001, 42, 7041. Furans as versatile synthons for target-oriented and diversity-oriented synthesis 02AG(E)3192 02AG(E)4560 02BMCL3271 02CEJ4255 02EJO1051 02H209 02H479 02JOC2919 02JOC3412 02JOC7361 02OL1515 02OL1771 02S1993 02T3801 02T5441 02T10469 02TL943 02TL1705 02TL4381 02TL4753 02TL9155 03ARK43 03BMC3261 03COC1443 03JA36 03JOC6847 03OBC3592 03OL941 03SCI613 03SL735 03T6819 O3T10181 03TL1161 03TL4467 03TL7411 03TL8227 04HCA1493 04H583 04JA9106 04JA14095 04JNP1039 04JOC6931 04OL465 04OL2189 04OL3241 31 M.

Transition metal promoted coupling also features in the synthesis of naphtho[2,l-6]pyrans 16 linked to thiophene units through an alkyne function. Apart from a shift in the absorption maximum, Synthesis and photochromic properties of naphthopyrans 43 these compounds have similar photochromic properties to the simple 3,3-diphenyl derivative <00HCA3043>. However, when two naphthopyran units are connected at the 3-positions through a 5,5'-(2,2'-bithienyl) moiety the pyran rings are opened sequentially on irradiation at 366 nm.

Res. 1998, 314, 25. Y. G. H. D. Harman, J. Am. Chem. Soc. 1998,120, 509. R. Ballini, G. Bosica, J. Nat. Prod. 1998, 61, 673. C. J. K. Cha, J. Org. Chem. 1998, 63, 2804. P. V. A. C. W. A. Collins, J. Org. Chem. 1998, 63, 6914. A. Rodriguez, M. W. J. Godfroid, Eur. J. Org. Chem. 1999, 2655. L. Wright H. R. Hoffmann, Eur. J. Org. Chem. 1999, 2991. T. K. S. E. R. J. Danishefsky, J. Am. Chem. Soc. 1999,121, 6563. D. Mance, B. Borovicka, B. Karaman, K. Jakopcic, J. Heterocycl. Chem. 1999, 36, 1337. Y.

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