81411-56-5Relevant articles and documents
A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities
Aggarwal, Varinder K.,Alonso, Emma,Bae, Imhyuck,Hynd, George,Lydon, Kevin M.,Palmer, Matthew J.,Patel, Mamta,Porcelloni, Marina,Richardson, Jeffery,Stenson, Rachel A.,Studley, John R.,Vasse, Jean-Luc,Winn, Caroline L.
, p. 10926 - 10940 (2007/10/03)
A variety of metalated tosylhydrazone salts derived from benzaldehyde have been prepared and were reacted with benzaldehyde in the presence of tetrahydrothiophene (THT) (20 mol %) and Rh2(OAc)4 (1 mol %) to give stilbene oxide. Of the lithium, sodium, and potassium salts tested, the sodium salt was found to give the highest yield and selectivity. This study was extended to a wide variety of aromatic, heteroaromatic, aliphatic, α,β-unsaturated, and acetylenic aldehydes and to ketones. On the whole, high yields of epoxides with moderate to very high diastereoselectivities were observed. A broad range of tosylhydrazone salts derived from aromatic, heteroaromatic, and α,β-unsaturated rated aldehydes was also examined using the same protocol in reactions with benzaldehyde, and again, good yields and high diastereoselectivities were observed in most cases. Thus, a general process for the in situ generation of diazo compounds from tosylhydrazone sodium salts has been established and applied in sulfur-ylide mediated epoxidation reactions. The chiral, camphor-derived, [2.2.1] bicyclic sulfide 7 was employed (at 5-20 mol % loading) to render the above processes asymmetric with a range of carbonyl compounds and tosylhydrazone sodium salts. Benzaldehyde tosylhydrazone sodium salt gave enantioselectivities of 91 ± 3% ee and high levels of diastereoselectivity with a range of aldehydes. However, tosylhydrazone salts derived from a range of carbonyl compounds gave more variable selectivities. Although those salts derived from electron-rich or neutral aldehydes gave high enantioselectivities, those derived from electron-deficient or hindered aromatic aldehydes gave somewhat reduced enantioselectivities. Using α,β-unsaturated hydrazones, chiral sulfide 7 gave epoxides with high diastereoselectivities, but only moderate yields were achieved (12-56%) with varying degrees of enantioselectivity. A study of solvent effects showed that, while the impact on enantioselectivity was small, the efficiency of diazo compound generation was influenced, and CH3CN and 1,4-dioxane emerged as the optimum solvents. A general rationalization of the factors that influence both relative and absolute stereochemistry for all of the different substrates is provided. Reversibility in formation of the betaine intermediate is an important issue in the control of diastereoselectivity. Hence, where low diastereocontrol was observed, the results have been rationalized in terms of the factors that contribute to the reduced reversion of the syn betaine back to the original starting materials. The enantioselectivity is governed by ylide conformation, facial selectivity in the ylide reaction, and, again, the degree of reversibility in betaine formation. From experimental evidence and calculations, it has been shown that sulfide 7 gives almost complete control of facial selectivity, and, hence, it is the ylide conformation and degree of reversibility that are responsible for the enantioselectivity observed. A simple test has been developed to ascertain whether the reduced enantioselectivity observed in particular cases is due to poor control in ylide conformation or due to partial reversibility in the formation of the betaine.
Oxyanionic Substituent Effect on the C-H Insertion of Carbenes. Reaction of Alkoxides with Dichlorocarbene and Chlorophenylcarbene
Harada, Toshiro,Akiba, Eiji,Oku, Akira
, p. 2771 - 2776 (2007/10/02)
The lithium alkoxides of benzylic, allylic, and simple alkyl alcohols were allowed to react with chloroform in the presence of t-BuOLi in THF-hexane to give, in 32-91percent yields, dichloromethylcarbinols, which were produced by the insertion of dichlorocarbene into the α C-H bond of alkoxides but not by the Wittig rearrangement of carbanions of alkyl dichloromethyl ethers.The enhanced reactivity toward dichlorocarbene of the α C-H bond of alkoxides was clearly demonstrated by the high selectivity of the insertion.The potassium alkoxides of a series of analogous alcohols reacted analogously with benzal chloride in the presence of t-BuOK in THF to give the corresponding substituted oxiranes (16-79percent); e.g., the reaction of potassium benzyl oxide gave 2,3-diphenyloxirane (79percent) as a mixture of stereoisomers (trans:cis = 1.0).With 2-phenethoxide, n-octyl oxide, or 2-methoxyethoxide, the corresponding dialkyl acetals of benzaldehyde were also formed in 9, 6, and 6percent yield, respectively, and their formation is explained in terms of nucleophilic attack of alkoxide on chlorophenylcarbene.With trans-crotyl oxide or 2-phenetoxide, 1,3-diphenylpropan-1-one(33percent) and 1-phenylpent-3-en-1-one (6percent) were produced, respectively, as byproducts through the isomerization of the primary product oxiranes.Oxiranes were produced by the insertion of chlorophenylcarbene into the α C-H bond of alkoxides followed by the cyclization of the intermediate 1-substituted 2-chloro-2-phenethyl alkoxide.These reactions provide us with new preparative methods of synthetically useful dichloromethyl carbinols and oxiranes.
