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

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

ISBN-10: 0080447112

ISBN-13: 9780080447117

ISBN-10: 0080458564

ISBN-13: 9780080458564

This can be the 17th annual quantity of development in Heterocyclic Chemistry, which covers the literature released in the course of 2004 on lots of the very important heterocyclic ring platforms. the amount opens with really good stories: Dennis Wright covers Furans as flexible Synthons for Target-Oriented and Diversity-Oriented Synthesis; and John Hepworth and Mark Heron talk about 'The Synthesis and Photochromic houses of Naphthopyrans'. the rest chapters learn the hot literature at the universal heterocycles so as of accelerating ring measurement and the heteroatoms current. * contains 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 experiences on flexible Synthons for Target-Oriented and Diversity-Oriented Synthesis; and Synthesis and Photochromic houses of Naphthopyrans

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Leon, J. Plumet, Tetrahedron Lett. 1996, 37, 8957. A. D. E. Schnute, J. Am. Chem. Soc. 1997,119, 7897. L. Duan, R. W. Rees, J. Chem. Soc, Perkin Trans. 1 1997, 1617. A. Padwa, M. G. H. Wu, J. Org. Chem. 1997, 62, 4088. M. Lautens, E. Fillion, J. Org. Chem. 1997, 62,4418. P. Yu, Y. Y. W. C. Wong, J. Org. Chem. 1997, 62, 6359. H. Kitajima, T. Katsuki, Synlett 1997, 568. T. Taniguchi, K. Nakamura, K. Ogasawara, Synthesis 1997, 509. K. Tsuboi, Y. M. Jiang, A. Naganavva, M. Isobe, Tetrahedron 1997, 53, 5123.

The half-lives vary between 1 and 6 minutes, with the thiophene analogues exhibiting faster fade rates than the furan derivatives. D. M. Heron [2,3-g]indole example absorbs in the visible region and is yellow; the open form has Xmax 480, 590 ran and a half-life of 30 minutes <01WOP34609>. 2 5-Membered heterocyclic rings fused across the g-face. g. 1) unlike the corresponding naphtho[2,3-6]pyran is photochromic and shows better colourability, though faster fading, than the naphtho[2,l-6]pyran <96CJC1649>.

Gilchrist, R. Mendonca, J. Chem. Soc. Perkin Trans. 1 2001, 2969. 01JOC2400 O. Arjona, R. Menchaca, J. Plumet, J. Org. Chem. 2001, 66, 2400. 01JOC3119 A. A. Brodney, M. Dimitroff, B. H. Wu, J. Org. Chem. 2001, 66, 3119. 01OL107 O. Arjona, R. Menchaca, J. Plumet, Org. Lett. 2001, 3, 107. J. Donohoe, A. A. Linney, M. Helliwell, Org. Lett. 2001, 3, 861. 01OL929 A. J. R. Hoffmann, Org. Lett. 2001, 3, 929. 01OL1315 C. Bohm, O. Reiser, Org. Lett. 2001, 3, 1315. L. C. Usher, M. Estrella-Jimenez, Org. Lett.

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A Critical Review of the 2004 Literature Preceded by Two Chapters on Current Heterocyclic Topics by Gribble Prof , Gordon Gribble , John Joule Prof Gribble Prof


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