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Molecular Molecular things you things you want want Molecular Molecular things you things you have have ? ? chemists chemists

Organic Synthesis

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Molecular things you have. Organic Synthesis. chemists. ?. Molecular things you want. Nam Le. Molecular things you have. Molecular things you want. Synthesis Requires Two Things. 1. a library of reactions. 2. a strategy or plan for combining known reactions to reach - PowerPoint PPT Presentation

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Page 1: Organic Synthesis

Molecular Molecular things you things you

wantwant

Molecular Molecular things you things you

havehave

??chemistschemists

Page 2: Organic Synthesis

Molecular Molecular things you things you

wantwant

Molecular Molecular things you things you

havehave

Nam LeNam Le

Page 3: Organic Synthesis

Synthesis Requires Two ThingsSynthesis Requires Two Things

1. a library of reactions1. a library of reactions

2. a strategy or plan for combining2. a strategy or plan for combining known reactions to reachknown reactions to reach the desired target moleculethe desired target molecule

3. and a little luck always helps3. and a little luck always helps

Page 4: Organic Synthesis

goalgoal(a desired molecular structure)(a desired molecular structure)

Page 5: Organic Synthesis

goalgoal

subgoal-subgoal-1a1a

subgoal-subgoal-1b1b

subgoal-subgoal-2a2a

subgoal-subgoal-2b2b

subgoal-subgoal-3a3a

subgoal-subgoal-3b3b

Work the problem Work the problem from the final goal from the final goal toward the reactants.toward the reactants.

Have a library of Have a library of reactions that reactions that connect a goal to a connect a goal to a subgoal.subgoal.

Page 6: Organic Synthesis

Work the problem Work the problem from the final goal from the final goal toward the reactants.toward the reactants.

Have a library of Have a library of reactions that reactions that connect a goal to a connect a goal to a subgoal.subgoal.

OH

O

Br

BrBr

Br

Using your Using your knowledge of knowledge of each reaction each reaction select the best select the best pathway as your pathway as your solution to the solution to the synthetic synthetic problem.problem.

Page 7: Organic Synthesis

Work the problem Work the problem from the final goal from the final goal toward the reactants.toward the reactants.

Have a library of Have a library of reactions that reactions that connect a goal to a connect a goal to a subgoal.subgoal.

OH

O

Br

BrBr

Br

Using your Using your knowledge of knowledge of each reaction each reaction select the best select the best pathway as your pathway as your solution to the solution to the synthetic synthetic problem.problem.

Page 8: Organic Synthesis

OO

H3C

OH

CH3

H3C

HO

OH

CH3

CH3

CH3

OH

CH3

OCONH2

CH3

DiscodermolideDiscodermolide

The result of biological studies stimulated considerable interest in The result of biological studies stimulated considerable interest in discodermolide as a possible discodermolide as a possible immunosuppressantimmunosuppressant. .

Subsequently studies demonstrated discodermolide is a potent Subsequently studies demonstrated discodermolide is a potent cell growth inhibitory agent, which arrests cell development at the cell growth inhibitory agent, which arrests cell development at the M phase by binding and stabilizing mitotic spindle microtubules. M phase by binding and stabilizing mitotic spindle microtubules. Thus, the ability of (+)-Thus, the ability of (+)-1 1 to inhibit cell growth was suggested to to inhibit cell growth was suggested to resemble the clinically proven resemble the clinically proven anticanceranticancer agent Taxol. agent Taxol.

Page 9: Organic Synthesis

OO

H3C

OH

CH3

H3C

HO

OH

CH3

CH3

CH3

OH

CH3

OCONH2

CH3

DiscodermolideDiscodermolide

isolated from a isolated from a marine spongemarine sponge

Page 10: Organic Synthesis

OO

H3C

OH

CH3

H3C

HO

OH

CH3

CH3

CH3

OH

CH3

OCONH2

CH3

DiscodermolideDiscodermolide

Some problems with pharmaceuticals from natural Some problems with pharmaceuticals from natural sources:sources:Quantities can be very limited.Quantities can be very limited.

More active structural variants are not available from More active structural variants are not available from nature.nature.

The isolation process can be very expensive.The isolation process can be very expensive.Industrial production can destroy valuable Industrial production can destroy valuable ecosystems.ecosystems.

Page 11: Organic Synthesis

DiscodermolideDiscodermolide

Some problems with pharmaceuticals from natural Some problems with pharmaceuticals from natural sources:sources:Quantities can be very limited.Quantities can be very limited.

More active structural variants are not available from More active structural variants are not available from nature.nature.

The isolation process can be very expensive.The isolation process can be very expensive.Industrial production can destroy valuable Industrial production can destroy valuable ecosystems.ecosystems.

CH3

O

CH3

OCONH2

CH3

Page 12: Organic Synthesis

OO

H3C

OH

CH3

H3C

HO

OH

CH3

CH3

CH3

OH

CH3

OCONH2

CH3

DiscodermolideDiscodermolide

isolated from a isolated from a marine spongemarine sponge

Page 13: Organic Synthesis

OO

H3C

OH

CH3

H3C

HO

OH

CH3

CH3

CH3

OH

CH3

OCONH2

CH3

DiscodermolideDiscodermolide

chemical chemical synthesissynthesis

available available chemicalchemicalss

Page 14: Organic Synthesis

OO

H3C

OH

CH3

H3C

HO

OH

CH3

CH3

CH3

OH

CH3

OCONH2

CH3

DiscodermolideDiscodermolide

chemical chemical synthesissynthesis

OO

H3C

OTBS

CH3

OTBSO CH3

OTBS

CH3

O

CH3

O

PMP

XPMBO

H3C

X

OH

CH3

CH3

Page 15: Organic Synthesis

OO

H3C

OTBS

CH3

OTBSO CH3

OTBS

CH3

O

CH3

O

PMP

XPMBO

H3C

X

OH

CH3

CH3

N

OH O

OCH3

CH3

PMBO

HO OCH3

O

commerciallcommercially availabley available

Page 16: Organic Synthesis

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H HPd .

HOH PCC O

C XC

R OHH Br

R Br ..

Page 17: Organic Synthesis

General Scheme of a new reaction:General Scheme of a new reaction:

R1 C C HNa NH2

R1 C C

R1 C C CH2 RR CH2 Br

R1 C C

A+ HB B H + A

Page 18: Organic Synthesis

Example. :Example. :

H H

muscalure, the sex muscalure, the sex attractant of the attractant of the common houseflycommon housefly

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

H2/Pd

6 11

6

11

Br

H

Br

6

1. 2. NH2

Page 19: Organic Synthesis

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

Page 20: Organic Synthesis

General Reaction Scheme of a new General Reaction Scheme of a new reaction:reaction:

C OH

H BrC O

H

H

+

Br

CBr

+

OHH

R OHH Br

R Br ..

A+ HB B H + A

Page 21: Organic Synthesis

Work the problem from the Work the problem from the final goal toward the final goal toward the reactants.reactants.

Have a library of reactions that Have a library of reactions that connect a goal to a subgoal.connect a goal to a subgoal.

Using your knowledge of each Using your knowledge of each reaction select the best pathway as reaction select the best pathway as your solution to the synthetic your solution to the synthetic problem.problem.

Problems in synthetic Problems in synthetic chemistrychemistry

Page 22: Organic Synthesis

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less

OH

OHH /H2O H /H2O

??

Page 23: Organic Synthesis

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less

OH

H /H2O

H2/Pd

Br

1.

HBr

2. NH2

Page 24: Organic Synthesis

from compounds containing 2 carbon atoms or less

OH

H /H2O

H2/Pd

Br

1.

HBr

2. NH2

Page 25: Organic Synthesis

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less

OH

OH

H /H2OH /H2O

Page 26: Organic Synthesis

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less

OHH /H2O

H

Br

OH

HBr

1. BH3 2. H2O2/OH

H2/Pd

Page 27: Organic Synthesis

H O

H

OHH

H

.

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less

OH

H

Br

OH

HBr

1. BH3 2. H2O2/OH

H2/PdH

Br

H /H2OH2/Pd

Page 28: Organic Synthesis

from compounds containing 2 carbon atoms or less

OH

H

Br

OH

HBr

1. BH3 2. H2O2/OH

H2/PdH

Br

H /H2OH2/Pd

Page 29: Organic Synthesis

H O

H

OHH

H

.

1. BH3

2. H2O2/OH H

OH .

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less H

O

Page 30: Organic Synthesis

H O

H

OHH

H

.

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less H

O

H

Br

OH

HBr

1. BH3 2. H2O2/OH

H2/Pd

H2/Pd

OHPCC

1. BH3 2. H2O2/OH

1. BH3

2. H2O2/OH H

OH .

Page 31: Organic Synthesis

H O

H

OHH

H

.

H H

H

H

Pd/C

.

H H

H H .Pd

HOH PCC O

C XC

R OHH Br

R Br ..

from compounds containing 2 carbon atoms or less H

O

H

Br

OH

HBr

1. BH3 2. H2O2/OH

H2/PdH

Br

H2/Pd

OHPCC

1. BH3 2. H2O2/OH