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2000 amino alcohols amino alcohols (acyclic compounds) P 0130 33 - 069 Enantioselective Synthesis of lyxo-(2R,3R,4R)-C 18 -Phytosphingosine Using Double Stereodifferentiation. Key steps in the synthesis of title compound (VIII) from known lactol (I) are a microwave assisted retro-DAR, a highly stereoselective Overman rearrangement, and an asymmetric dihydrox- ylation which provides a further example for the matched pair case in double stereodifferentiation. — (MARTIN, CATHERINE; PRUENCK, WILLIAM; BORTOLUSSI, MICHEL; BLOCH, ROBERT; Tetrahedron: Asymmetry 11 (2000) 7, 1585-1592; Lab. Carbocycles, CNRS, Inst. Chim. Mol. Orsay, Univ. Paris-Sud, F-91405 Orsay, Fr.; EN) 1

ChemInform Abstract: Enantioselective Synthesis of lyxo-(2R,3R,4R)-C18-Phytosphingosine Using Double Stereodifferentiation

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2000 amino alcohols

amino alcohols (acyclic compounds)P 0130

33 - 069Enantioselective Synthesis of lyxo-(2R,3R,4R)-C18-PhytosphingosineUsing Double Stereodifferentiation. — Key steps in the synthesis oftitle compound (VIII) from known lactol (I) are a microwave assisted retro-DAR,a highly stereoselective Overman rearrangement, and an asymmetric dihydrox-ylation which provides a further example for the matched pair case in doublestereodifferentiation. — (MARTIN, CATHERINE; PRUENCK, WILLIAM;BORTOLUSSI, MICHEL; BLOCH, ROBERT; Tetrahedron: Asymmetry 11(2000) 7, 1585-1592; Lab. Carbocycles, CNRS, Inst. Chim. Mol. Orsay, Univ.Paris-Sud, F-91405 Orsay, Fr.; EN)

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