An unprecedented combination of high chemo- and stereoselectivity in the NaBH4 reduction of 1+1 complexes between albumin and aromatic 1,3-diketones results in the formation of anti 1,3-diols with de up to 96%.
Albumin-controlled stereoselective reduction of 1,3-diketones to anti-diols / Benedetti, Fabio; Berti, Federico; Donati, Ivan; Fregonese, Massimo. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 8(2002), pp. 828-829.
Albumin-controlled stereoselective reduction of 1,3-diketones to anti-diols
BENEDETTI, FABIO;BERTI, FEDERICO;DONATI, IVAN;
2002-01-01
Abstract
An unprecedented combination of high chemo- and stereoselectivity in the NaBH4 reduction of 1+1 complexes between albumin and aromatic 1,3-diketones results in the formation of anti 1,3-diols with de up to 96%.File in questo prodotto:
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