A Decennary Journey towards the Efficient Asymmetric Hydrogenation of Highly Functionalized Ketones. Issue 6 (7th July 2016)

• Record Type: Journal Article
• Authors: Li, Wanfang; Lu, Bin; Zhang, Zhaoguo
• Is Part Of: Chemical record. Volume 16:Issue 6(2016)
• Page Start: 2506
• Page End: 2520
• Publication Date: 2016-07-07
• Subjects: asymmetric catalysis -- chemoselectivity -- hydrogenation -- ketones -- ruthenium; Chemistry -- Periodicals; 540
• DOI: 10.1002/tcr.201600064
• Languages: English
• ISSNs: 1527-8999

Abstract

Abstract: Around 2006, our group launched a long‐term project on the asymmetric hydrogenation of functionalized ketones by using ruthenium complexes with SunPhos ligands. In this review, we recount the burgeoning and blossoming of this project. At the outset, we attempted some benchmark reactions with an array of monofunctionalized ketones, including α‐ and β‐keto esters/amides, β‐keto sulfones, phosphonates, and α‐hydroxy ketones. For α‐keto esters and amides, we discovered that CeCl3 7H2 O was an efficient additive for both activity and enantioselectivity. The element iodine was found to be a valid additive for β‐keto sulfones. β, γ‐Unsaturated α‐keto acids and esters were also hydrogenated to the saturated chiral blocks with good enantioselectivity and a high turnover number. For the α‐substituted β‐keto esters and phosphonates, exceptionally high stereoselectivity was achieved through dynamic kinetic resolution. Based on these incipient successes, we diverted to bifunctionalized ketone substrates, such as γ‐heteroatom‐substituted β‐keto esters and δ‐ketal‐β‐keto esters. For the δ‐ketal‐β‐keto esters, CaCO3 was added to stabilize the δ‐ketal groups, which ensured the formation of δ‐ketal‐β‐hydroxy esters in good yields and high ee values. More interestingly, γ‐halo‐γ, δ‐unsaturated‐β‐keto esters were hydrogenated to afford highly enantiopure chiral allyl alcohols under mild and neutral conditions. The distance effect of the directing groups was investigated in β‐, γ‐, and δ‐keto amides; the last two were hydrogenated with the Ru–SunPhos–diamine system. To implement the pinpoint recognition of two carbonyl groups in similar chemical propinquity, we compared the reaction rates of different β‐keto acid derivatives. THF was found to be a helpful coordinative solvent to control the chemo‐ and enantioselectivity for more challenging polycarbonyl substrates, such as 3‐oxo glutaric acid derivatives, β, δ‐diketo carboxamides, and γ‐heteroatom‐substituted β‐diketones. The effects of solvents and heteroatoms in these substrates were also studied. Applications of these hydrogenation reactions were also exemplified by the employment of the products for important pharmaceutical syntheses. Abstract : Opening up the scope : Using the Ru–SunPhos complex as a catalyst, the chemo‐ and enantioselective hydrogenation of a range of highly functionalized ketones, including γ‐heteroatom‐substituted β‐keto esters, δ‐ketal‐β‐keto esters, γ‐halo‐γ, δ‐unsaturated‐β‐keto esters, 3‐oxo glutaric acid derivatives, β, δ‐diketo carboxamides, and γ‐heteroatom‐substituted β‐diketones, has been realized. These substrates are very challenging, but useful for organic synthesis.