Convenient access to cyclopentenones is provided by catalytic intra- and intermolecular Pauson - Khand reactions in the presence of octacarbonyldicobalt and tributylphosphane sulfide (see scheme). In contrast to other reactions of this type, they proceed under mild conditions (70 degrees C, 1 atm CO), and commercially available [Co(2)(CO)(8)] can be used without further purification.
Einen leichten Zugang zu Cyclopentenonen bieten katalytische, intra‐ und intermolekulare Pauson‐Khand‐Reaktionen in Gegenwart von Octacarbonyldicobalt und Tributylphosphansulfid (siehe Schema). Im Unterschied zu anderen Reaktionen dieses Typs verlaufen die hier beschriebenen unter milden Bedingungen (70 °C, 1 atm CO), und handelsübliches [Co2(CO)8] kann ohne weitere Reinigung als Katalysator verwendet werden.
The treatment of O-glycoside with alcohol in the presence of montmorillonite K10 clay and 4-Å MS yields the 1,4-aryl migration product with a 1,2-cis-phenyl C-glycoside scaffold and a chiral silyl moiety with high stereoselectivity.Aryl C-glycosides constitute an important class of the Cglycoside family of natural products and have attracted considerable interest because of their diverse biological activities and resistance to acidic and enzymatic hydrolysis. 1 Therefore a number of methods have been developed for the stereoselective formation of the aryl C-glycoside linkage. 2 Among these methods, the reactions of glycosyl donors by intermolecular Friedel-Crafts couplings or by reactions with aryl metal reagents have been well established and these reactions yielded 1,2-trans-aryl C-glycosides, predominantly. In contrast, access to the thermodynamically more unfavorable 1,2-cis-aryl C-glycosides remains relatively undeveloped. 3 To this end, we have recently reported that montmorillonite K10 clay promoted 1,4-aryl or alkenyl migration from silicon to the C1 carbon in cyclic N,O-acetal systems. 4-6 The unique features of this reaction are as follows: (i) the aryl or alkenyl group on the siloxy group migrates intramolecularly in a cis fashion, and (ii) a concomitant nucleophilic substitution of the alkoxy group on the silicon atom proceeds with high stereoselectivity. On the basis of this result, we envisioned that a similar aryl migration of O-glycoside A with a tert-butyldiphenylsilyl group at the C2 hydroxyl group could afford the phenyl C-glycosides B in a 1,2-cis fashion (Scheme 1). Desilylation of B would provide C2 hydroxy phenyl C-glycoside C. Furthermore, the treatment of phenyl C-glycosides B with a base would cause b-elimination and provide enantioenriched silanols D, which are otherwise difficult to obtain. Here, we report the details of the aryl migration in cyclic acetal systems, which provide an effective approach to the stereoselective synthesis of 1,2-cis-phenyl C-glycosides as well as chiral silanol.At the outset, we attempted the phenyl migration of the simple five-membered cyclic hemiacetal 1a with the (tertbutyldiphenylsilyl)oxy group at the C2 position; the cyclic hemiacetal 1a was easily prepared from commercially available (S)-a-hydroxy-g-butyrolactone (97% ee) in two steps [(i) TBDPSCl, imidazole and (ii) DIBAL]. The reaction was performed according to the previously developed protocol; the cyclic hemiacetal 1a was treated with two equivalents of benzyl alcohol in the presence of K10 and 4-Å MS in CH 2 Cl 2 at 0 °C for 12 hours, providing the corresponding aryl migration product 2 in 71% yield with 90% diastereomeric ratio (Scheme 2). 7,8 Some of the aryl migration product 2 may be produced through benzyl acetal 1b; indeed a similar reaction of separately prepared 1b 9 also provided 2 in 46% yield with 90% dr.The exposure of the phenyl migration product 2 to TBAF afforded alcohol 3a as a single diastereomer, which means that the diastereomer of 2 is derived from the silicon stereocenter. T...
ring closure reactions ring closure reactions O 0130
-047Phosphane Sulfide/Octacarbonyldicobalt-Catalyzed Pauson-Khand Reaction under an Atmospheric Pressure of Carbon Monoxide.-Several phosphane chalcogenides are examined as ligands in the title reaction of enyne (Ia) with CO. The best results are obtained with tributylphosphane sulfide. Under these optimized conditions, other enynes give good yields of the expected products. The three-component reaction of olefin (VI), alkyne (VII), and CO can also be carried out with excellent yield by using the same conditions.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.