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Synthesis Without Protecting Croups

In order to overcome this internal incompatibility, one tends to protect the amino function in 7 as an amide, whereupon the reaction sequence can be carried out requiring at the end a final deprotection of the amine to reach the target 9. [Pg.215]

The most common cause of the use of protecting groups is the necessity to differentiate between two (or more) similar functional groups. Let it be alcohol groups in a polyol. For instance, a differentiation between the primary and secondary [Pg.215]

Handbook of Green Chemistry Volume 7 Green Synthesis, First Edition. Edited by Chao-Jun Li. [Pg.215]

It is easy to project that differentiation of a higher number of hydroxyl groups (functional groups) in a polyol such as one faces in carbohydrate chemistry may [Pg.216]

The BOM group likewise is orthogonal to the TBS group and serves to differentiate that particular hydroxyl group to be unveiled at later stage of the synthesis. [Pg.218]


See other pages where Synthesis Without Protecting Croups is mentioned: [Pg.215]    [Pg.224]    [Pg.226]    [Pg.232]    [Pg.234]    [Pg.215]    [Pg.224]    [Pg.226]    [Pg.232]    [Pg.234]   


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Synthesis without Protections

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