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 very important heterocyclic ring structures. the quantity 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 talk about 'The Synthesis and Photochromic houses of Naphthopyrans'. the remainder chapters research the hot literature at the universal heterocycles so as of accelerating ring dimension and the heteroatoms current. * contains new contributions from specialists within the box* Covers literature released in the course of 2004 on lots of the vital heterocyclic ring platforms * provides stories on flexible Synthons for Target-Oriented and Diversity-Oriented Synthesis; and Synthesis and Photochromic houses of Naphthopyrans

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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. J. C. G. M. Cabrejas, Tetrahedron: Asymmetry 1997, 8, 1623. L. Battistini, F. Zanardi, G. Rassu, P. Spanu, G. G. B. Ferrari, G. Casiraghi, Tetrahedron: Asymmetry 1997, 8, 2975.

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.

Scheme 30 De Clercq <02EJO1051> utilized an intramolecular furan Diels-Alder reaction for model studies relating to ll-oxo-10a-steroids. Treating enone 226 with an aluminum catalyst at low termperatures induced a stereoselective cycloaddition to produce 227 in reasonable yield. Hudlicky studied the cyclodextrin-promoted Diels-Alder reaction of furyl oxazolidine 228 in an approach to morphinans. A transannular Diels-Alder of a furanophane has been studied by Deslongchamps <99TL2765; 03JOC6847> in the context of a synthesis of anhydrochatancin.

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