The reaction mixture was quenched with few drops of MeOH, evaporated and extracted http://www.selleckchem.com/products/Bleomycin-sulfate.html with EtOAc (2 × 50 mL). afforded 9 (1.1 g, 73%) as a colorless oil. [α]D −37.4 (c 0.18, CHCl3); 1H NMR (300 MHz, CDCl3): δ 5.89 (m, 1H, olefinic), 5.11 (q, 2H, J = 14.8 Hz, olefinic), 4.02 (m, 1H,

–CH), 3.83 (m, 1H, –CH), 1.60–1.37 (m, 4H, 2× –CH2), 1.06 (d, 3H, J = 5.4 Hz, –CH3), 0.84 (s, 9H, 3× –CH3), 0.01 (s, 6H, 2× –CH3); 13C NMR (75 MHz, CDCl3): δ 141.5, 114.3, 73.1, 68.6, 35.1, 32.9, 26.0, 23.3, 18.0, −4.4, −4.8; IR (KBr): 3386, 2929, Palbociclib solubility dmso 2857, 1465, 1373, 1253, 1134, 1048, 833 cm−1. To a cooled (0 °C) solution of 9 (3.0 g, 12.29 mmol) in dry THF (30 mL), NaH (0.59 g, 24.59 mmol) was added, stirred for 30 min and treated with a solution of PMBBr (2.93 g, 14.74 mmol) in dry THF (15 mL). After 7.5 h stirring at room temperature, the reaction mixture was quenched with sat. NH4Cl solution (10 mL) and extracted with ethyl acetate (2 × 50 mL). The organic layers were washed with water (2 × 10 mL), brine (10 mL) and dried (Na2SO4).

Solvent was evaporated under reduced pressure and purified the residue by column chromatography (60–120 Silica gel, 5% EtOAc in pet. ether) to furnish 16 (3.7 g, 82%) as a yellow liquid. [α]D +26.6 (c 0.7, CHCl3); 1H NMR (300 MHz, CDCl3): δ 7.20 (d, 2H, J = 8.6 Hz, ArH-PMB), 6.83 (d, 2H, J = 8.6 Hz, ArH-PMB), 5.87 (m, 1H, olefinic), 5.19 (q, 2H, J = 4.1, 11.6 Hz, olefinic), 4.54, 4.28 (2d, 2H, J = 11.6 Hz, –OCH2 Ar), 3.78 (m, 1H, –CH), 3.69 (s, 3H, –OCH3), 3.62 (m, 1H, –CH), 1.61–1.32 (m, 4H, 2× –CH2), 1.20 Resminostat (d, 3H, J = 6.0 Hz, –CH3), 0.81 (s, 9H, 3× –CH3), 0.03 (s, 6H, 2× –CH3); 13C NMR (75 MHz, CDCl3): δ 149.8, 131.1, 128.5, 128.8, 127.6, 120.9, 72.7, 57.8, 55.3, 35.8, 30.2, 24.9, 23.8, 22.4, −4.3; IR (neat): 3427, 2926, 2863, 1739, 1456, 1268, 1108 cm−1. Ozone was bubbled through a cooled (−78 °C) solution of 16 (5.2 g, 24.19 mmol) in CH2Cl2 (70 mL) until

the pale blue color persisted. Excess ozone was removed with Me2S (2 mL) and stirred for 30 min at 0 °C. The reaction mixture was concentrated under reduced pressure to give aldehyde, which was used for further reaction. To a solution of was dissolved in benzene (50 mL) (methoxycarbonylmethylene)-triphenyl phosphorane (2.5 g, 7.37 mmol) was added at reflux. After 2 h, solvent was evaporated to furnish 17 (2.25 g, 87%) as a yellow liquid. [α]D +45.6 (c 1.4, CHCl3); 1H NMR (CDCl3, 300 MHz): δ 7.20 (d, 2H, J = 8.0 Hz, ArH-PMB), 6.89 (d, 2H, J = 8.0 Hz, ArH-PMB), 6.61 (dd, 1H, J = 6.1, 15.7 Hz, olefinic), 5.76 (d, 1H, J = 15.6 Hz, olefinic), 4.33 (d, 1H, J = 11.7 Hz, benzylic), 4.16 (d, 1H, J = 11.7 Hz, benzylic), 3.81 (m, 1H, –OCH), 3.67 (s, 3H, OCH3), 3.61 (s, 3H, OCH3), 3.