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Why Bother with Disconnections

When you are ready to start, cover the first page with a card and pull it down to reveal the first frame. Read and act on that frame, then reveal frame 2 and so on. If you are unfamiliar with the disconnection approach, I suggest you read the introduction Why bother with disconnections so that you can see what I m driving at. Otherwise the first sections of the programme may seem rather pointless. [Pg.2]

The aim of this programme is that you should learn how to design an organic synthesis for yourself. Supposing you wanted to make this compound  [Pg.2]

Here the first disconnection ( a) was of a C-N bond, the second ( b ) of a C-C bond taking us back to compounds (7) and (8)  [Pg.3]

These are in fact standard disconnections which you will meet in sections G and C of the programme. The first part of the programme (Sections B to H) shows you how to use disconnections and which disconnections are good ones. The second part shows you how to choose between alternative series of disconnections to get good synthetic schemes. [Pg.3]

Disconnection An analytical operation, which breaks a bond and converts a molecule into a possible starting material. The reverse of a chemical reaction. Symbol = and a curved line drawn through the bond being broken. Called a dislocation by some people. [Pg.4]

FGI Functional Group Interconversion The operation of writing one functional group for another so that disconnection becomes possible. Again the reverse of a chemical reaction. Symbol with FGI written over it. [Pg.4]

Reagent A compound which reacts to give an intermediate in the planned synthesis or to give the target molecule itself. The synthetic equivalent of a synthon. [Pg.4]


See other pages where Why Bother with Disconnections is mentioned: [Pg.2]    [Pg.6]    [Pg.6]    [Pg.7]    [Pg.7]    [Pg.2]    [Pg.2]    [Pg.6]    [Pg.6]    [Pg.7]    [Pg.7]    [Pg.2]   


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