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|Section2= |Section3= }} Carpanone is a naturally occurring lignan-type natural product most widely known for the remarkably complex way nature prepares it, and the similarly remarkable success that an early chemistry group, that of Orville L. Chapman, had at mimicking nature's pathway.〔C.W. Lindsley, C.R. Hopkins & G.A. Sulikowski, 2011, Biomimetic synthesis of lignans, In "Biomimetic Organic Synthesis" (E. Poupon & B. Nay, Eds.), Weinheim: Wiley-VCH, ISBN 9783527634767, see (), accessed 4 June 2014.〕〔O.L. Chapman, M.R. Engel, J.P. Springer & J.C. Clardy, 1971, Total synthesis of carpanone, ''J. Am. Chem. Soc.'' 93:6697–6698.〕 Carpanone is an organic compound first isolated from the carpano trees (''Cinnamomum sp.'') of Bougainville Island by Brophy and coworkers, trees from which the natural product derives its name.〔〔F. Liron, F. Fontana, J.-O. Zirimwabagabo, G. Prestat, J. Rajabi, C. La Rosa & G. Poli, 2009, A New Cross-Coupling-Based Synthesis of Carpanone, Org. Lett., 11(19):4378–4381, DOI: 10.1021/ol9017326, see () or (), accessed 4 June 2014〕 The hexacyclic lignan is one of a class of related diastereomers isolated from carpano bark as mixtures of equal proportion of the "handedness" of its components (i.e., racemic mixtures), and is notable in its stereochemical complexity, because it contains five contiguous stereogenic centers. The route by which this complex structure is achieved through biosynthesis involves a series of reactions that, almost instantly, take a molecule with little three-dimensionality to the complex final structure. Notably, Brophy and coworkers isolated the simpler carpacin, a phenylpropanoid with a 9-carbon framework, recognized its substructure as being dimerized within the complex carpanone structure,〔G.C. Brophy, J. Mohandas, M. Slaytor, T.R. Watson & L.A. Wilson, 1969, Novel lignans from a ''Cinnamomum'' sp. from Bougainville, Tetrahedron Lett. 10:5159-5162.〕 and proposed an hypothesis of how carpacin was converted to carpanone in plant cells: * carpacin underwent loss of a methyl (-CH3) group from the ring methoxy (-OCH3) group to provide the phenol, desmethylcarpacin, * this phenol intermediate then underwent a phenolic coupling to generate a dimeric intermediate, which was * followed immediately by a Diels-Alder (4+2) cycloaddition reaction to create 2 new rings, to give the final carpanone product. Remarkably, within two years, Chapman and coworkers were able to chemically design a route to mimic this proposed biosynthetic route, and achieved the synthesis of carpanone from carpacin in a single "pot", in about 50% yield.〔〔 Carpanone itself is limited in its pharmacologic and biologic activities, but related analogs arrived at by variations of the Brophy-Chapman approach have shown activities as tool compounds relevant to mammalian exocytosis and vesicular traffic,〔Brian C. Goess, Rami N. Hannoush, Lawrence K. Chan, Tomas Kirchhausen, and Matthew D. Shair, 2006, Synthesis of a 10,000-Membered Library of Molecules Resembling Carpanone and Discovery of Vesicular Traffic Inhibitors, ''J. Am. Chem. Soc.'' 128(16): 5391–5403, DOI: 10.1021/ja056338g, see (), accessed 4June 2014.〕 and provided therapeutic "hits" in antiinfective, antihypertensive, and hepatoprotective areas.〔 The original Chapman design and synthesis is considered a classic in total synthesis, and one that highlights the power of biomimetic synthesis.〔 ==Total synthesis== The first total synthesis of carpanone was the biomimetic approach published by Chapman ''et al.'' in 1971. The required desmethylcarpacin (2-allylsesamol), shown below as the starting molecule in the scheme, is acquired in two high-yield steps involving three transformations: * allylation of the phenolic anion generated after treatment of sesamol with potassium carbonate and allyl bromide, * followed by a thermal Claisen rearrangement to move the O-allyl group onto the adjacent site on the aromatic ring, and then * thermal isomerization of the Claisen product, to move the terminal olefin (alkene) into conjugation with the ring (with e.g., potassium ''tert''-butoxide as base). This procedure is one of several that gives the required desmethylcarpacin (carpacin with the methyl of its methoxy group removed).〔 Though oxidative dimerizations of phenols normally used a 1-electron oxidant, Chapman then followed a precedent involving a 2-electron oxidant and treated desmethylcarpacin with PdCl2 in the presence of sodium acetate (e.g., dissolved in a mixture of methanol and water);〔〔 the reaction was perceived to proceed via a complexation of a pair of carpacins to the Pd(II) metal via their phenolic anions (as shown in scheme, below right),〔 followed by a classic 8-8' (β-β') oxidative phenolic coupling of the two olefin tails—shown crossing in the image—to give a dimeric ''trans''-''ortho''-quinone methide-type of lignan intermediate. A particular conformation of this dimer then places a 4-electron enone of one ring over the 2-electron enol of the other (shown adjacent in image for clarity), setting the state for a variant of the Diels-Alder reaction termed an inverse demand Diels-Alder reaction (see curved arrows in image), which closes the 2 new rings and generates the 5 contiguous stereocenters. The carpanone is produced in yields of ≈50% by the original method, and in yields >90% in modern variants (see below).〔〔〔 The synthesis of a single diastereomer was confirmed in the original Chapman work, using X-ray crystallography. For the elegance of its "one-pot construction of a tetracyclic scaffold with complete stereocontrol of five contiguous stereo centers",〔 the original Chapman design and synthesis is "()ow considered a classic in total synthesis" that "highlights the power of biomimetic synthesis".〔〔 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Carpanone」の詳細全文を読む スポンサード リンク
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