Enantioselective preparation of C2-symmetrical 1,4-diols
摘要:
The catalytic enantioselective addition of functionalized dialkylzincs to the γ-alkoxyaldehydes 5, 6 and 7 provides 1,4-diols 1–3 with 73–99 %ee. After a simple reaction sequence, these diols are converted to chiral γ-alkoxyaldehydes which undergo a second catalytic enantioselective addition of the same diorganozinc providing C 2 -symmetrical 1,4-diols 10a–f with excellent diastereoselectivity (up to 97 : 3).
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DOI:
10.1016/S0040-4039(00)78200-1
被引量:
年份:
1994
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来源期刊
Tetrahedron Letters
8 August 1994
引用走势
2010
被引量:33
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