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Synlett 2003(5): 0651-0654
DOI: 10.1055/s-2003-38349
LETTER
© Georg Thieme Verlag Stuttgart ˙ New York

Organic Reactions in Water: Optimization of the Synthesis of (±)-Manzamenone A Using Surfactant Catalysts

Jeremy R. Doncaster, Hazel Ryan, Roger C. Whitehead*
Department of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK
Fax: +44(161)2754939; e-Mail: roger.whitehead@man.ac.uk;
Further Information

Publication History

Received 21 February 2003
Publication Date:
28 March 2003 (online)

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Abstract

Improved procedures exploiting surfactant catalysts have been developed for the conversion of (±)-untenone A to (±)-manzamenone A in an aqueous medium. The consequent availability of (±)-manzamenone A has allowed the synthesis of a biologically interesting cyclopropyl analogue of the natural product.

Key words

catalysis - cycloaddition - natural product - total synthesis

    References

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8

Cyclopropyl compounds of type 4 were of interest as potential alkylating agents of DNA and therefore as candidates for anti-cancer screening.

13

Representative Procedure for the Preparation of 1a from 2 Using SDS:
A mixture of H2O (13 mL) and SDS (0.65 g) was stirred at 25 °C for 5 min when untenone A (2) (50 mg, 0.13 mmol) was added. The reaction mixture was stirred rapidly for 6 h at 25 °C when it was extracted with EtOAc (3 ¥ 20 mL). The combined organic extracts were washed with brine (20 mL), H2O (20 mL), dried (MgSO4) and concentrated in vacuo to give a solid. This solid was taken up in the minimum volume of EtOAc (ca. 5 mL) and filtered in order to remove any remaining SDS. The filtrate was concentrated in vacuo to give a crude product, which was purified by flash column chromatography [SiO2; gradient elution: EtOAc:petroleum ether (40:60), 1:5, to neat EtOAc] to give manzamenone A (36 mg, 75%) with spectroscopic data identical to those reported previously.

16

Representative Procedure for the Preparation of 1a from 2 Using BASC 5
A mixture of water (1 mL) and BASC 5 (4.2 mg, 0.013 mmol) was stirred at 25 °C for 5 min when untenone A(2) (50 mg, 0.13 mmol) was added. The reaction mixture was stirred rapidly for 7.5 h, when brine (5 mL) and a sat. aq solution of NaHCO3 (5 mL) were added. Organic material was extracted into EtOAc (3 ¥ 7 mL) and the combined organic extracts were dried (MgSO4) and concentrated in vacuo to give the crude product. Purification by flash column chromatography [SiO2; gradient elution: EtOAc-petroleum ether (40:60), 1:5, to neat EtOAc] gave manzamenone A (33 mg, 69%) with spectroscopic data identical to those reported previously.

17

Representative Procedure for the Preparation of 1a from 2 Using LASC 6
A similar procedure to that used for BASC 5 [H2O (3 mL); LASC 6 (11mg, 0.013 mmol); untenone A (50 mg, 0.13 mmol); reaction time, 1 h] gave manzamenone A (35 mg, 73%) after purification by flash column chromatography.

21

Data for compound 11: Colourless solid, mp 62-64 °C. IR(film): 1762 (C=O), 1741 (C=O), 1722 (C=O) cm-1. 1H NMR (300 MHz, CDCl3): δ = 0.90 [6 H, br t, J = 6.8 Hz, C(26)H3 and C(42)H3], 1.20-1.60 [58 H, m, C(12)H2 to C(25)H2 and C(27)H2 to C(41)H2], 1.62 [1 H, d, J = 5.3 Hz, one of C(9)H2], 1.84 [1 H, d, J = 5.3 Hz, one of C(9)H2], 2.14 [2 H, br t, J = 7.5 Hz, C(11)H2], 2.55 [1 H, dd, J = 9.3, 4.8 Hz, C(1)H], 3.11 [1 H, dd, J = 9.3, 5.4 Hz, C(6)H], 3.28 [1 H, d, J = 4.8 Hz, C(2)H], 3.53 [1 H, br, C(5)H], 3.58 (3 H, s, CO2CH3), 3.77 (6 H, s, 2 ¥ CO2CH3), 5.70 [1 H, d, J = 1.1 Hz, C(4)H]. 13C NMR (75.4 MHz, CDCl3): δ = 14.39 [C(26)H3 and C(42)H3], 22.96, 27.31, 27.98, 28.17, 29.45, 29.64, 29.81, 29.87, 29.90, 29.94, 29.99, 32.20 [C(12)H2 to C(25)H2 and C(27)H2 to C(41)H2, many overlapping], 36.71 [C(11)H2], 38.80 [C(1)H], 41.62 [C(5)H], 42.49 [C(6)H], 44.01 [C(2)H], 44.93, 45.25 [C(8) and C(10)], 52.36, 52.59 and 52.88 (3 ¥ CO2CH3), 122.78 [C(4)H], 138.23 [C(3)], 168.31, 171.52, 174.65 [C(43), C(44) and C(45)], 205.84 [C(7)]. MS (APCI+): m/z (%) = 772 (65) [MH+], 771 (100). (Found: 771.6135. C48H83O7 requires 771.6139).