Unified Synthesis of Polycyclic Alkaloids by Complementary Carbonyl Activation

Abstract A complementary dual carbonyl activation strategy for the synthesis of polycyclic alkaloids has been developed. Successful applications include the synthesis of tetracyclic alkaloids harmalanine and harmalacinine, pentacyclic indoloquinolizidine alkaloid nortetoyobyrine, and octacyclic β‐carboline alkaloid peganumine A. The latter synthesis features a protecting‐group‐free assembly and an asymmetric disulfonimide‐catalyzed cyclization. Furthermore, formal syntheses of hirsutine, deplancheine, 10‐desbromoarborescidine A, and oxindole alkaloids rhynchophylline and isorhynchophylline have been achieved. Finally, a concise synthesis of berberine alkaloid ilicifoline B was completed.

Despite the advancement of combinatorial strategies, natural products remain an indispensable source for the discovery of new molecular entities. [1] Their diverse scaffolds with hydrogen bond donor and acceptor groups positioned in a well-defined spatial arrangement make them attractive starting points and inspiration for drug development. [2] Bioactive polycyclic alkaloids, such as yohimbine (1), hirsutine (2), deplancheine (3), eburnamonine (4), ilicifoline B (5), peganumine A (6), and reserpine (7), contain the common quinolizidine core I fused to different heterocyclic rings ( Figure 1). We reasoned that developing a straightforward annulation method for efficient construction of these scaffolds is beneficial for the total synthesis of polycyclic natural products and their analogs. Since the indole substructure is a privileged [3] and very common motif in these polycyclic natural products, we started our synthetic journey with the quinolizidine-fused indole core. We strategized that incorporating an enamide motif into the A ring would provide a flexible handle for subsequent transformations. Therefore, intermediate III [4] was considered the central linchpin for a divergent synthesis [5] of polycyclic alkaloids. It was envisioned to be derived from IV by an annulation sequence involving an electrophilic cyclization followed by lactamization. Toward this goal we identified two major challenges: 1) selective activation of the amide carbonyl group to participate in the electrophilic cyclization; [6] 2) subsequent selective activation of the second carbonyl group to achieve lactamization.
We conceived a one-pot approach in which IV can be prepared by two-fold condensation of V, VI and active ester component. By permutation of the substrates V and VI, a variety of polycyclic ring system with diverse substitution patterns could be accessed (Scheme 1).
In order to orchestrate the subsequent activations, we initially investigated the reaction using the amide 8 a as the model substrate (for its preparation see the Supporting  Information). We tested different conditions to achieve selective amide activation via reactive nitrilium ions, [3] including a variety of phosphorus(V) reagents frequently applied in the Bischler-Napieralski reaction [7] and the von Braun amide degradation (Table 1, entries 1-4). [8] We also screened strong electrophiles, such as Me 3 SiCl and (COCl) 2 , [9] and the Tf 2 O/2-chloropyridine system [10] which have been used successfully in electrophilic amide activation recently ( Table 1, entries 5-7). Most of these conditions afforded tricyclic imine 9 a as the major product. Unfortunately, the subsequent imine acylation to give tetracyclic product turned out to be challenging. With POCl 3 , 10 was isolated in 6 % yield along with 84 % of imine 9 a (Table 1, entry 1). This result indicated that the reaction had stopped after the first cyclization. We hypothesized that imine-enamine tautomerization during second cyclization and the leaving ability of the alkoxyl group could also be the critical prerequisites for the second cyclization. [11] After a screening of bases (see the Supporting Information), we achieved a slight improvement to 10 % yield of 10 using K 2 CO 3 ( Table 1, entry 8). With nBu 4 NBr as phase transfer catalyst and methanol, the yield of 10 was further increased to 18 % (Table 1, entry 9). Inspired by active ester activation strategies used in peptide synthesis, [12] we tested a variety of ester derivatives (see the Supporting Information). Satisfyingly, with 1,1,1,3,3,3-hexafluoro-2-propoxy ester 8 d, we achieved a 90 % yield of 10 ( Table 1, entry 12).
With optimized conditions in hand, we explored the scope of the reaction for the synthesis of diverse polycyclic scaffolds (Table 2). Substitutions at the indole ring with electron donating groups (12 a and 12 b) and electron withdrawing groups (12 c and 12 d) were well tolerated, providing the corresponding tetracyclic scaffolds in good yields (76-86 %).
Encouraged by these results, we investigated additional substitution patterns and ring systems. Substituting the quinolizidine core afforded the tetracycles 12 e-12 j in good  [a] Reactions were performed with substrate (0.10-4.7 mmol) using the standard procedure (yields are for the isolated product). See the Supporting Information for details.
yields (64-83 %) thus providing access to the indoloquinolizidine-type alkaloid nortetoyobyrine (12 j) [13] in an additional step. The 7/6, 8/6, 6/7 and 6/8 fused ring systems were obtained in moderate yield (12 k-12 n, 26-52 %). Finally, we successfully expanded our strategy to benzene derivatives and heteroaromatic compounds, such as furan, thiophene, and benzothiophene (12 o-12 x, 33-91 %). We next turned our attention to manipulations in the A ring in order to fully exploit our scaffold for natural product synthesis (Scheme 2). Through oxidation, a second double bond could be easily introduced to the 3,4-position (VII). Reduction of the double bond in the 1,2-position (VIII) could be achieved with or without concomitant reduction of the lactam. Moreover, introduction of a carbonyl group in 4position (IX) was key to the synthesis of more complex natural product.
Racemic 15 can be obtained through selective catalytic hydrogenation of 10 using palladium on carbon (Scheme 4). From this intermediate, selenoxide elimination affords 16, a key intermediate in the total synthesis of hirsutine (2), rhynchophylline (17) and isorhynchophylline (18). [17] An asymmetric reduction of the C À C double bond was realized using chiral phosphoric acid (CPA) 19 and Hantzsch ester (20) system [18] to give 15 in 80 % ee and 61 % yield. This material can be converted into (S)-deplancheine (3) and (S)-10desbromoarborescidine A (21) as previously reported. [19] To further demonstrate the synthetic potential of this method, we envisioned to use our annulation in a protectinggroup-and transition-metal-free asymmetric total synthesis of peganumine A (6). [20] Following the established protocol, we successfully prepared the tetracyclic intermediate 25 in 85 % yield (Scheme 5). Subsequently, ketoenamide 26 was

Angewandte Chemie
Communications obtained in 50 % yield through a two-step a-oxidation sequence. The tert-butoxycarbonyl (Boc) derivative of 26 constitutes an intermediate in Zhus elegant total synthesis of peganumine A (6). [21] At this point, we contemplated the possibility of a protecting-group-free synthesis. The key cascade cyclization was achieved using 0.2 equivalents of TFA in toluene to complete a protecting-group-free synthesis of (AE)-6 in 42 % yield.
Encouraged by the success of the previous cascade cyclization, we initiated investigations toward an asymmetric total synthesis. First, we tested the chiral thiourea (CTU, Figure 2) and PhCO 2 H system developed by Jacobsen, [22] which afforded 92 % ee in Zhus synthesis [21] for the Bocprotected substrate. In our protecting-group-free substrate, with 27 and PhCO 2 H, the enantioselectivity was 9 % ee (Table 3). We speculated that the remarkable difference in enantioselectivity could be attributed to an impaired recognition between substrate and catalyst. It is possible that either the Boc group is crucial for the recognition, or that the free aketoenamide 26 interrupted the substrate binding. Based on these considerations, we proposed to either apply a multibinding-site catalyst to rigidify the transition state, or to use asymmetric counteranion directed catalysis (ACDC) [23] as stronger chiral acid to activate the imine more efficiently.
First, we tested the conjugate-base-stabilized Brønsted acid (CBSBA) 28 developed by Seidel, [24] and 1,2,3,4,5pentacarboxycyclopentadiene (PCCP) derived pentamenthyl ester 29, a novel CÀH acid discovered by Lambert, [25] which are all multi-binding-site catalysts. However, no improvement of the enantioselectivity could be achieved with our substrate. Moving to the ACDC using CPA-2 (30), a significant improvement of the enantioselectivity (31 % ee) was observed. Expanding on this idea, we applied the stronger chiral Brønsted acid disulfonimide (DSI) [26] to the reaction and obtained 79 % ee with DSI-1 (31). Encouraged by this promising result, and after intensive screening of DSIs (see the Supporting Information), we finally discovered that using DSI-2 (32) could achieve 97 % ee and 81 % yield.
berberine alkaloid xylopinine (37) according to the reported method. [30] In summary, we have developed an efficient method that is enabling to the rapid assembly of polycyclic scaffolds of bioactive alkaloids, through a straightforward annulation reaction featuring a complementary carbonyl activation strategy. Diverse polycyclic ring systems were accessed in good yields, enabling the total synthesis of different types of alkaloids and their analogs. Through diverging pathways, the total synthesis of five alkaloids and formal total synthesis of six alkaloids were completed. Among them, a synthesis of (+)and (À)-peganumine A (6) was achieved in a protectinggroup-free sequence using a DSI catalyzed Pictet-Spengler reaction as the key step. Finally, we also applied this method to a synthesis of dimeric berberine alkaloid ilicifoline B (5).