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

Abstract

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 Rh(2)(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, alpha,beta-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 alpha,beta-unsaturated 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 alpha,beta-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 CH(3)CN 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...

Effect of sulfide structure on enantioselectivity in catalytic asymmetric epoxidation of aldehydes: Mechanistic insights and implications

“…Betaine formation can be rendered less reversible by either increasing the barrier to reversion to ylide and aldehyde or by reducing the barrier to bond rotation of the cisoid conformer to the transoid conformer. It had been established that the use of protic solvents or metal ions solvated the charges in the intermediate betaine and made their separation, which occurs during bond rotation, more facile (17,19). More facile separation results in reduced reversibility in betaine formation.…”

“…been established that betaine formation was again less reversible at low temperature (19). Reactions were performed with sulfonium salts 21 and 22, because the yields of our catalytic chemistry are diminished by the presence of significant amounts of water (17).…”

“…This chiral sulfide could be recovered in high yield and reused without any loss of asymmetric induction. A broad range of aldehydes, including aromatic, aliphatic, and certain ␣,␤-unsaturated aldehydes, could be converted into the corresponding epoxides in generally high yield with high levels of enantioselectivity and diastereoselectivity (17). Sulfide 1 could also be used in a stoichiometric variant of this process, which allows access to epoxides that are difficult to form using the catalytic protocol (18).…”

Tosylhydrazone – neue Anwendungen klassischer Reagentien in palladiumkatalysierten Kreuzkupplungen und metallfreien Umsetzungen

“…Die Verwendung von Tosylhydrazonsalzen für die Erzeugung von Metall-Carben-Komplexen in katalytischen Prozessen wurde von Aggarwal et al [5] eingeführt und in mehreren Prozessen erfolgreich genutzt, beispielsweise in Olefinierungen, Epoxidierungen, Cyclopropanierungen sowie C-H-und N-H-Insertionsreaktionen. Diese Chemie Tosylhydrazone sind wertvolle Zwischenverbindungen, die in der organischen Chemie seit fast 60 Jahren Anwendung finden.…”

Synthesis and elaboration of trans 2,3-diaryloxiranes

“…A range of aldehydes have been used in this process with phenyl tosylhydrazone salt and good selectivity was observed with aromatic and heteroaromatic aldehydes. 33 Pyridyl aldehydes proved to be incompatible with this process, presumably due to the presence of a nucleophilic nitrogen atom, which can compete with the sulfide for the metallocarbene to form a pyridinium ylide. Sulfide loadings as low as 5 mol % could be used in many cases.…”