Tetrahydrofurans and γ‐Lactones, VI. – Optically Active N‐Boc‐δ‐Amino‐γ‐lactones from Cyclooctyne and Furan The stereoselective synthesis of the title compounds (−)‐(2′R,8S)‐2b and (+)‐(2′S,8R)‐2b from (2′R,8R)1a and (2′S,8S)‐1a is described. The unprotected amino lactone 2c undergoes rearrangement to the γ‐hydroxy‐δ‐lactam 3a by treatment with hydrogen chloride.
No takes yet. Share an insight, caveat, or question.
Meints et al. (1993) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: