Synthesis of an optically active intermediate 4b for the A-ring of 1a,25-dihydroxyvitamin D3 analogs has been achieved in eight steps, starting from readily available, inexpensive D-(+)-xylose.
Two chiral building blocks 1 and 2 for anti-and syn-1, 3-diols has been achieved in 8 steps and 7 steps respectively, starting from the readily available and inexpensive D (+)-xylose 3.
文摘Synthesis of an optically active intermediate 4b for the A-ring of 1a,25-dihydroxyvitamin D3 analogs has been achieved in eight steps, starting from readily available, inexpensive D-(+)-xylose.
文摘Two chiral building blocks 1 and 2 for anti-and syn-1, 3-diols has been achieved in 8 steps and 7 steps respectively, starting from the readily available and inexpensive D (+)-xylose 3.