Quan
Gong
a,
Jialin
Wen
*ab and
Xumu
Zhang
*ac
aDepartment of Chemistry, Southern University of Science and Technology, 1088 Xueyuan Road, Shenzhen, 518055, China. E-mail: wenjl@sustech.edu.cn; zhangxm@sustech.edu.cn
bAcademy of Advanced Interdisciplinary Studies, Southern University of Science and Technology, 1088 Xueyuan Road, Shenzhen, 518055, China
cShenzhen Grubbs Institute, Southern University of Science and Technology, 1088 Xueyuan Road, Shenzhen, 518055, China
First published on 21st May 2019
We herein report an efficient method to synthesize cyclic hydroxy ketones with a chiral quaternary center. Catalyzed by an Ir/f-ampha complex, cyclic α,α-disubstituted 1,3-diketones were hydrogenated, giving mono-reduced products with both high enantioselectivities and diastereoselectivities. In addition, CC and CC bonds could survive in this catalytic system. This method was applied in the preparation of (+)-estrone. No diols were observed in this chemical transformation. The enantiomeric and diastereomeric induction were achieved as a result of steric hindrance.
The construction of this important synthon, however, is limited to enzyme catalyzed reduction,12,13 Ru-catalyzed transfer hydrogenation14,15 and Corey–Bakshi–Shibata9 reduction with borane. These methods suffer from the drawbacks of narrow substrate scope, moderate selectivity and high catalyst loading. The challenges of mono-reduction of cyclic α,α-disubstituted 1,3-diketones lie in areas such as (1) enantioselectivity and diastereoselectivity being realized in one step and (2) the prevention of over-reduction to diols. In the hydride transfer step, different facial approaches towards the substrate lead to two pairs of diastereomers (marked with blue and red arrows in Fig. 2). Enantioselectivity originates in the differentiation of a quaternary carbon from a methylene group (Fig. 2).
Our group has been dedicated to transition metal catalyzed ketone reduction during the recent two decades and has developed a series of ferrocene-based tridentate ligands for iridium catalyzed hydrogenation.16–18 A variety of simple or functionalized ketones can be hydrogenated to chiral alcohols with remarkably high ees and turnover numbers (TONs). To the best of knowledge, direct hydrogenation has not been applied in the preparation of the aforementioned synthon. Due to our continuous interest in construction of chiral molecules via transition metal catalyzed asymmetric hydrogenation, we envisioned that this efficient catalytic system could be applied in the mono-reduction of 1,3-diketones (Scheme 1).
Entry | Ligand | Conversionb | drc | eec |
---|---|---|---|---|
a Reaction conditions: 1a (0.1 mmol, 0.1 M), 1a/[Ir(COD)Cl]2/ligand/base = 500/0.5/1.1/10, 20 atm H2, rt, 1 h. b Conversion was determined by 1H NMR analysis, no by-product was observed. c dr and ee were determined by HPLC on a chiral stationary phase. | ||||
1 | f-amphox | 24% | 7.3/1 | 93% |
2 | Indan-f-amphox | 11% | 5.4/1 | 28% |
3 | f-amphol | 50% | 4.1/1 | 37% |
4 | f-ampha | 84% | 10.1/1 | 95% |
Extending the reaction time and increasing the hydrogen pressure drove this reaction to a full conversion. Interestingly, no over-reduction product (diol) was observed under harsher conditions. After careful optimization [for detailed condition screening, see ESI†], we finally obtained satisfactory conditions: catalyzed by an Ir/f-ampha complex (0.1% loading), the symmetric 1,3-diketone was reduced in dichloromethane in the presence of sodium tert-butoxide, giving the corresponding chiral hydroxy ketone with 99% ee and 21/1 dr. To our delight, no diol was observed in the crude reaction mixture. The turnover number of this reaction could reach 10000 without obvious reduction of stereoselectivities (Scheme 2).19
We applied the optimized conditions to explore the scope of this method with 0.1% catalyst loading. Various substitution groups on the benzene ring, no matter whether electron-withdrawing or electron-donating groups, did not bring significant changes in both the stereoselectivity and conversion (2a to 2j). 1,3-Diketones with an allyl group, instead of benzyl, were hydrogenated with high enantioselectivities as well as satisfactory diastereoselectivities (2k to 2m). In addition to alkenes, the alkynyl group also survives in this chemical transformation (2n). The preference of reducing polar CO bonds demonstrated its chemoselectivity. To our surprise, a dialkyl substrate also worked well in this reaction (2o and 2p). This excellent stereoselectivity indicated that this catalytic system could discriminate two different alkyl groups (methyl vs. ethyl and methyl vs. propyl). Discrimination between simple alkyl groups has always been a top challenge in asymmetric catalysis, while alkyl and aryl groups are easy to differentiate (2q). When we expanded the ring size of the substrate from five to six, the performance faded and moderate stereoselectivities were obtained (2r). α,α-Disubstituted 1,3-indandiones could also be hydrogenated, giving desired yields and stereoselectivities (2s and 2t).
This reaction could be scaled up smoothly (Scheme 3, top). In order to exploit the potential applications of this method in synthetic chemistry, we chose (+)-estrone as a target. This molecule plays a key role in steroidogenesis20 and chemical synthesis of steroids.7,21,22 We followed Corey's route,9 as well as List's route,23 to synthesize Torgov's 1,3-diketone24 in a sub-gram scale. Hydrogenation of this diketone under the optimized conditions quantitatively gives a hydroxy ketone with >99% ee and 8:1 dr. After Prins cyclization/dehydration and oxidation with IBX, Torgov's diene24 was obtained25 which could be easily converted to (+)-estrone by a two-step transformation.23
Scheme 3 Scale-up reaction and application of desymmetrization via hydrogenation in the synthesis of (+)-estrone. |
Our curiosity was drawn by the phenomenon of only one carbonyl group being reduced. When applying harsh conditions, it was also difficult to form diols (Scheme 4, eqn (1)). The purified product 2a could not yield a diol under these forcing conditions as well (eqn (2)). Hydrogenation under the same conditions with the other enantiomer of the ligand, however, also failed in this transformation (eqn (3)). The chiral pocket of both catalyst enantiomers seemed not to be compatible with the hydroxy ketone. Reduction of 2a with sodium borohydride exclusively gave a chiral trans-diol in a quantitative yield. After protecting the hydroxyl group, however, reduction of this ketone with sodium borohydride under the same conditions exclusively gave a cis-diol (Scheme 4, eqn (5)). Plausible explanations included an intramolecular hydride transfer after the formation of a boron alkoxide, which could be a result of transesterification of borate.26–28
While reduction of a five-membered-ring cyclic 1,3-diketone by both sodium borohydride and iridium catalyzed hydrogenation gave the same diastereoselectivity, the reduction of the six-membered-ring substrate was different. Hydrogenation under the optimized conditions gave an alcohol with the –OH cis to the larger benzyl group, but mono-reduction with sodium borohydride29 yielded the other diastereomer30 (Scheme 5). These results indicated the same facial preference of iridium catalyzed hydrogenation and sodium borohydride reduction in the five-membered ring but a different facial preference in the six-membered ring.
Scheme 5 Comparison of Ir-catalyzed hydrogenation and sodium borohydride reduction in desymmetrization of cyclic diketones. |
Footnote |
† Electronic supplementary information (ESI) available. CCDC 1906351, 1906353 and 1906354. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c9sc01769k |
This journal is © The Royal Society of Chemistry 2019 |