Metathesis in Natural Product Synthesis: Strategies, by Janine Cossy, Stellios Arseniyadis, Christophe Meyer, Robert

By Janine Cossy, Stellios Arseniyadis, Christophe Meyer, Robert H. Grubbs

Emphasizing the effect of metathesis in common product synthesis during the kinds of key reactions, it is a accomplished view of a sizzling subject. Written via most sensible foreign authors, this prepared reference is obviously established and filled with very important info, together with consultant experimental techniques for useful applications.A actual must-have for somebody operating in ordinary product synthesis.

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Trauner et al. 11) [14]. The cyclization precursor was prepared via an asymmetric ene reaction of glyoxylate 72. Further transformations led to 1,6-diene 74 that could be cyclized to cyclopentenone 75 in 86% yield using [Ru]-II (5 mol%). Conjugate addition of the organocuprate 76 then established the C11 quaternary stereocenter. The central seven-membered ring was then closed with an electrochemical oxidation. ) Karst. 2 Formation of Five-membered Carbocycles by RCM O R*O Steps R*O SnCl4, −78 °C O [Ru]-II (5 mol%) OH O 72 O 73 (dr = 10 : 1) R = (1S,2R )-2-Phenylcyclohexyl OBn Toluene, reflux 86% OBn O 74 75 Cu(CN)(2-Th)Li2 PO O 76: P = TBDPS 1.

Int. , 47, 6201–6203. Tiefenbacher, K. and Mulzer, J. (2008) Angew. Chem. Int. , 47, 6199–6200. J. (2008) Angew. Chem. Int. J. (2008) Angew. Chem. Int. , 47, 1780–1783; (c) Hayashida, J. H. (2008) Angew. Chem. Int. , 47, 4373–4376. , and Ihara, M. (2001) J. Am. Chem. , 123, 1856–1861. Ciochina, R. B. (2006) Chem. , 106, 3963–3986.

When possible, comparison between various catalysts and experimental conditions is also discussed. Challenging RCM was reported during the synthesis of the ABE tricyclic analogs 259 of the alkaloid methyllicaconitine (256), a competitive antagonist of nicotine acetylcholine receptors [63]. The B ring system was synthesized via a [Ru]-I catalyzed RCM of the 1,8-diene 257 possessing two contiguous quaternary stereogenic centers. 47). A key step in the total synthesis of (±)-frondosin B (260) reported by Mehta and Likhite is RCM of 1,8-diene 262 using [Ru]-I (C6 H6 , reflux) [64].

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