Wavelength dependent photoextrusion and tandem photo-extrusion reactions of ninhydrin bis-acetals for the synthesis of 8-ring lactones, benzocyclobutenes and orthoanhydrides

Ninhydrin bis-acetals give access to 8-ring lactones, benzocyclobutenes and spirocyclic orthoanhydrides through photoextrusion and tandem photoextrusion reactions. Syntheses of fimbricalyxlactone B, isoshihunine and numerous biologically-relevant heterocycles show the value of the methods, while TA-spectroscopy and TD-DFT studies provide mechanistic insights on their wavelength dependence.

The photodecarbonylation of ninhydrin bis-acetal 2 to benzocyclobutene 3 was developed by Butenschön et al. to provide low cost access to benzocyclobutenedione (Scheme 1). 1 Indeed, it remains the most convenient method for its synthesis in spite of the modest yield attained for the photoextrusion of carbon monoxide from 2. Consequently, when a need for benzocyclobutenedione arose, we decided to develop the reaction as a flow photochemical process in order to facilitate its optimisation with respect to wavelength, residence time, solvent and acetal protecting group. 2,3 In the event, we uncovered conditions leading to a modest yield improvement for benzocyclobutene 3 and discovered a wavelength dependence for the reaction giving high-yielding access to 8-ring lactone 5a and orthoanhydride 6. Herein we describe our development of those methods, together with demonstrations of their usefulness in heterocyclic and natural products synthesis, and a detailed mechanistic study by transient absorption (TA) spectroscopy and TD-DFT analysis.
Our investigation began with an examination of the wavelength dependence on the photoextrusion of carbon monoxide from bis-acetal 2. While all wavelengths studied led to the evolution of gas, which was vented from the system using a circulating flow technique (see ESI †), only UVA irradiation gave benzocyclobutene 3 as a significant product. 3,4 An optimum yield of 57% was realised when a 0.05 M solution of 2 in acetonitrile was irradiated with 30 Â 1.5 W UVA LEDs for residence time of 3 h. By contrast, irradiation of bis-acetal 2 with UVB or UVC light gave rise to a complex mixture of products on work-up that varied from experiment to experiment and contained no benzocyclobutene 3, vide infra. Curiously, when the same reaction was performed on the homologous ninhydrin bis-acetal 4a, 8-ring lactone 5a was given in high yield (Scheme 1). Various analogues of 5 carrying substituents on the acetals and arene also gave the reaction in high yield (Table 1). In general, bis-1,3-dioxanes with a symmetrical arene and/or acetal substitution pattern gave a single product in 80-90% yield, e.g. 5a-c. Substrates lacking those symmetry elements also gave high yields but led to isomeric mixtures, e.g. lactones 5d-g. Thought this limited the yield attained for individual products to B40%, in the context of medium ring synthesis such an outcome remains competitive. 5 Scheme 1 The discovery of wavelength and acetal dependence on the outcome of photoextrusion reactions involving ninhydrin bis-acetals.
To demonstrate the utility of the method, we next applied it in a total synthesis of fimbricalyxlactone B 11, a natural product from the roots of Strophioblachia fimbricalyx Boerl. (Euphorbiaceae) (Scheme 2). 6 Thus, bis-acetal 4h was formed from the corresponding 1-indanone 7 in 76% yield through sequential SeO 2 oxidation and acetalisation with 2,2-dimethylpropandiol. 7 Exposure of an acetonitrile solution of 4h to UVC light under circulating flow next gave a 3 : 2 mixture of lactones 5h and 5h 0 that was readily separated by column chromatography. Methanolysis of the major isomer 5h then gave ester 9 which was advanced to fimbricalyxlactone B 11 by ruthenium tetroxide oxidation to carboxylic acid 10 and acetal hydrolysis with HCl. 8 Importantly, the spectral and physical data recorded on our sample matched those reported for the natural product. Its identity was also confirmed by X-ray crystallographic analysis (Scheme 2, CCDC 1908866). † 6,9 The potential of these 8-ring lactones to serve as intermediates in heterocyclic synthesis was next demonstrated with the conversion of 5a to spirolactone 12 on acetal hydrolysis (Scheme 3). 9 In turn, its treatment with methylamine gave isoshihunine 13 in 77% yield, from which the alkaloids shihunidin 14 and shihunine 15 can each be derived. 10,11 Furthermore, reaction with hydrazines gave high yielding access to phthalazones (e.g. 16,17,21), which are important pharmacophores present in the chemotherapeutic agent olaparib (Lynparza s ), 12 and azelastine (Astelin, Optivar, Allergodil), a frontline drug treatment for mild rhinitis. 13 By contrast, o-phenylenediamine, ethanolamine and ethylenediamine gave lactols 18 -20 respectively.
The mechanistic course of the photoextrusion reaction was next studied by transient absorption (TA) spectroscopy following excitation of bis-acetal 4a in CH 3 CN at 266 nm (Scheme 4 and Fig. S1, ESI †). Analysis of the ps-TA spectra (Fig. S1a, ESI †) allowed us to extract the time constants associated with spectral evolution using global kinetic analysis. 14 The data could be fitted using two exponential decays with time constants t 1 = 1.8 AE 0.4 ps and t 2 = 1.8 AE 0.2 ns (Fig. S1b and c, ESI †). The observed transient spectrum at 1 ps time delay showed an absorption band at 585 nm which was assigned to the np* (S 1 ) excited state 1 [4a] following comparison of the extracted spectrum with that computed for the S 1 state (Fig. S7, ESI †). Decay of the S 1 state was associated with the formation of a new transient species with an absorption band at 454 nm. This was attributed to biradical 1 [22] based on comparison with results reported for the photoexcitation of 1,1,3-triphenyl-3-hydroxy-2indanone. 15 Additionally, the result aligns with a recent TA study of the C-C bond cleavage of cyclopentanone in cyclohexane following 255 nm photoexcitation, which Kao et al. found occurred in r1 ps. 16 Likewise the t 2 component [1.8 AE 0.2 ns] for the rate of formation of 3 [22] from 1 [22] is consistent with previously reported ISC timescales for acyl-alkyl diradicals. 17 Spectral evolution by ns-TA spectroscopy was also monitored (Fig. S1d, ESI †). Three exponentials are required to describe these data, with time constants t 1 = 4.8 AE 0.4 ns, t 2 = 100 AE 20 ns, and t 3 = long-lived ( Fig. S1e and f, ESI †). 17 The t 1 component was associated with a decay of the 460 nm band for 3 [22] with simultaneous formation of a new transient at 550 nm, attributed to the decarbonylation product 3 [23]. A similar transient spectral feature was reported for the decarbonylation of diphenylmethylacyl radical (Ph 2 MeCCO ) in isooctane, which had a rate constant k = 1.5 Â 10 8 s À1 . 15,18 Decay of the 550 nm transient species 3 [23], with t 2 = 100 AE 20 ns, was associated with the formation of a longlived transient at 440 nm assigned to quinodimethane 26. This is in line with the rate constant measured by Fujiwara et al. for the formation of o-xylylene from 2-indanone following photoexcitation at 266 nm in cyclohexane (k = 1.4 AE 0.1 Â 10 7 s À1 ). 19 Thus, the wavelength dependence of the reaction centres on the fate of longlived intermediate 26 (Scheme 4). Irradiation of 26 with UVA leads to a singlet excited state 1 [26] that can relax to benzocyclobutene 24. By contrast, its irradiation with UVB or UVC light gives rise to higher singlet excited states of 26 from which ISC to 3 [23] is allowed. Collapse of 3 [23] to biradical 25 then provides access to 8-ring lactone 5a.
Applying this mechanistic understanding to ninhydrin bisacetal 2 (Scheme 5) led us to conclude that the course of that reaction was also dictated by the nature of the excitation of quinodimethane intermediate 28. As before, its irradiation with UVA gives a singlet excited state 1 [28] from which benzocyclobutene 3 is derived. Similarly, irradiation with UVB or UVC light leads to biradical 3 [29], which in turn collapses to biradical 30. However, in this case, ring closure to e-lactone 27 is outpaced by the extrusion of ethene to biradical 31, a precursor of orthoanhydride 6. Indeed, the near quantitative formation of orthoanhydride 6 on photolysis of bis-acetal 2 with UVB or UVC light was confirmed by analysis of a concentrated product mixture before aqueous work-up (see ESI † for characterisation data).
A TD-DFT analysis of quinodimethane 28 provided additional support for the mechanism (Fig. 1). 20 In particular, it indicated that the energy provided by UVA irradiation (3.18 eV l max 390 nm) mirrored that required for the pp* transition S 0 -S 1 , and that ISC between S 1 of 1 [28] and T 1 of 3 [29] was forbidden as both had pp* character. 21 Consequently, irradiation of 28 with UVA induces cyclisation to benzocyclobutene 3. By contrast, the greater energy provided by UVB and UVC irradiation facilitates ISC from 1 [28] to 3 [29] via higher excited states where both the orbital symmetry and energy requirements can each be fulfilled. 21 As a result, irradiation of 28 with UVB or UVC gives orthoanhydride 6.
Finally, the use of orthoanhydride 6 as a phthalic anhydride surrogate (Scheme 6) was demonstrated with the phthalimide protection of various 11-amines under mild conditions leading to 30a-f. 22 Similarly, reactions with 21-amines gave the expected amides, e.g. 31 and 37, while bis-nucleophiles provided high yielding access to an array of biologically relevant nitrogen heterocycles 32-36, 38 and 39.
In conclusion, we have shown that the photodecarbonylation of ninhydrin bis-acetals is a wavelength dependent reaction that can be conducted on a gram scale to give benzocyclobutenes on UVA irradiation (60 W, B5 h), and orthoanhydrides or 8-ring lactones on UVB or UVC irradiation (36 W, B2 h). Notably, they formally constitute ring contraction, ring correlative, and ring expansion reactions, respectively. These versatile intermediates give access to a host of heterocycles, natural products, and pharmacophores. Mechanistic details have been delineated using computational and spectroscopic methods, including picosecond and nanosecond  We gratefully acknowledge financial support from EPSRC [EP/P013341/1, EP/L003325/1 and EP/K039466/1], the European Regional Development Fund [ERDF Interreg Va programme (Project 121)], and the University of Nottingham Green Chemicals Beacon.

Conflicts of interest
There are no conflicts of interest to declare.