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General Procedure for Glycoporphyrins (6 and 7) A solution of the metalloporphyrin (0.04 mmol) and Grubbs catalyst 2 (25% mol, 0.01 mmol) in degassed dry CH2Cl2 (2 mL) was heated at reflux, under argon, and the allyl sugar 5, dissolved in CH2Cl2 (1 mL, was immediately added by a syringe to the mixture. The reflux was kept as mentioned in Table 1. The solvent was evaporated and the residue was purified by flash chromatography using a gradient of toluene-EtOAc as the eluent. The products 6 and 7 were obtained as red solids after crystallization from PE. Selected Data for 6a Mp 171-172°C. 1H NMR (300.13 MHz, CDCl3, δ, 1.30 (s, 3 H, CH3, 1.47 (s, 3 H, CH3, 3.27 (s, 3 H, OCH3, 3.27 (dd, J, 8.3 and 9.7 Hz, 1 H, H-5′a, 3.47 (dd, J, 6.3 and 9.7 Hz, 1 H, H-5′b, 3.87 dd, J, 2.1 and 5.9 Hz, 2 H, CH
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