Cyclic monosaccharides, such as ribose, have an array of alcohol groups. HO OH +enantiomer A HO In some cases, the alcohol groups are cis to one another, in other cases they are trans. Frequently, only close structural mimics will function properly as possible drugs. As a result, we have a strong need to be able to place multiple alcohol groups with well-defined relative stereochemistry, as shown below. Give the reagents required for A and B HO OH Ribose OH B HO OH

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Question 3
Cyclic monosaccharides, such as ribose, have an array of alcohol groups.
HO
OH
+enantiomer
A
HO
In some cases, the alcohol groups are cis to one another, in other cases they are trans.
Frequently, only close structural mimics will function properly as possible drugs. As a result, we
have a strong need to be able to place multiple alcohol groups with well-defined relative
stereochemistry, as shown below.
Give the reagents required for A and B
HO
0. OH
OH
Ribose
B
HO
OH
Transcribed Image Text:Question 3 Cyclic monosaccharides, such as ribose, have an array of alcohol groups. HO OH +enantiomer A HO In some cases, the alcohol groups are cis to one another, in other cases they are trans. Frequently, only close structural mimics will function properly as possible drugs. As a result, we have a strong need to be able to place multiple alcohol groups with well-defined relative stereochemistry, as shown below. Give the reagents required for A and B HO 0. OH OH Ribose B HO OH
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