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Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes his Nobel- prizewinning development of titanium-based catalysts for stereoselective oxidation, the mechanism of their reactions, and their use in preparing esomeprazole. Conformational energy of cyclic alkanes illustrates the use of molecular mechanics. Synchronize when the speaker finishes saying “Remember what the point of this synthesis was?” Synchrony can be adjusted by using the pause(||) and run(>) controls. For copyright notice see final page of this file
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Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

Dec 20, 2015

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Page 1: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

Chemistry 125: Lecture 34

Sharpless Oxidation Catalysts and the Conformation

of Cycloalkanes

Professor Barry Sharpless of Scripps Research Institute describes his Nobel-

prizewinning development of titanium-based catalysts for stereoselective oxidation,

the mechanism of their reactions, and their use in preparing esomeprazole.

Conformational energy of cyclic alkanes illustrates the use of molecular mechanics.

Synchronize when the speaker finishes saying

“Remember what the point of this synthesis was?” Synchrony can be adjusted by using the pause(||) and run(>) controls.

For copyright notice see final page of this file

Page 2: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

RO

~ racemic• •

OR

ORO

OEtO

O CO2Et

TiRO

O

3) Chiral Catalysis by Titanium/Diethyltartrate

Ti(etc)

ROO ••

RO+Ti

O

O

O

Ti(etc)

OEtO

CO2Et

O

RO

Ti

O

O

O

Ti(etc)

OEtO

CO2Et94% e.e. (3% R)• •

with added

iPr2NEt(discovered in 2000)

n

*

RSR'

O Ti

O

O

O

Ti(etc)

OEtO

CO2Et

+

(for no obvious reason)

catalyticcycle

RO

ROO

SR R'

Chiral “Oxidizing

Agent”

RSR'

+O

RSR'

O

RSR'

Nobel Prize 2001

Page 3: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

THE HUMAN UMBILICAL CORD

Page 4: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 5: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 6: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

Michaelson and Oshima

Page 7: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

Ti V Cr

Mo

W

Mn

Tc

Re

Ru

Os

B C

Si

N

P

O

S

Se

Te

F

Cl

Br

I

Ti(OR)4

HOOC

COOH

OH

HO

R

R

"Weinsaure"

Tsutomu Katsuki’s famous “recipe”Stanford Chemistry Department (1980)

Page 8: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 9: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 10: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

R''R

R' OH

R'' R

O

R'OH

70 - 90% yield > 90% ee

(CH 3 ) 3 COOH, Ti (O i Pr) 4

CH2Cl2 , – 20°C

"O"

"O" L - (+) - diisopropyl tartrate (natural)

D - (–) - diisopropyl tartrate (unnatural)

Asymmetric Epoxidation of olefins

Page 11: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

R''R

R' OH

R'' R

O

R'OH

70 - 90% yield > 90% ee

(CH 3 ) 3 COOH, Ti (O i Pr) 4

CH2Cl2 , – 20°C

"O"

"O" L - (+) - diisopropyl tartrate (natural)

D - (–) - diisopropyl tartrate (unnatural)

Asymmetric Epoxidation of olefins

Tsutomu Katsuki’s discovery -- a memorable day

in 1980 at Stanford University!

Page 12: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 13: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 14: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

"A man in California just won a Nobel Prize for mixing paint and wine!"

Los Angeles Times, October, 2001

Page 15: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 16: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 17: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

N

S N

N

O

O

H

OO*

H

EtOOCCOOEt

OH

OH

N

S N

N

*O

O

O

H

(S)

(S)-Omeprazole 'Nexium'

TT ii (OiPr)4

(D)-(-)-Diethyl Tartrate

Launched by AstraZeneca in 2000

$$$

Tsutomu Katsuki's now Famous Recipe-- He discovered it on January 18th, 2002 at Stanford University!

+

+ +

Page 18: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.
Page 19: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

The Carvones

O O

(S) - ( + ) (R) - ( - )

Page 20: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

Stretch

Bend

Stretch-Bend

Torsion

Non-1,4-VDW

1,4-VDW

TOTAL

Cyclobutane Puckering(by Molecular Mechanics)

Torsion vs. Bend

Relaxed

0.77

16.07

-0.92

11.23

-0.26

2.35

29.24

Planar

0.66

13.48

-0.78

14.81

-0.28

2.27

30.16

Page 21: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

Stretch

Bend

Stretch-Bend

Torsion

Non-1,4-VDW

1,4-VDW

TOTAL

Cyclopentane Puckering(by Molecular Mechanics)

"Envelope"

Relaxed

0.31

2.14

-0.09

6.38

-0.51

3.19

11.42

Planar

0.19

0.51

0.02

11.53

-0.48

4.34

16.10

Page 22: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

e.g. What is the source of the barrier

to c-hexane ring flip?

two butanegauche eclipsed

(~7 kcal/mole)

But why does the plastic model click?Baeyer Angle Strain

+7°+5°

-3°

+5°

Like a plastic model, molecular mechanics is satisfying because

not only does it say what a structure should be, it can also say “why”.

Page 23: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

Are They “True”?

YES

Are Molecular MechanicsPrograms Useful?

NO

Page 24: Chemistry 125: Lecture 34 Sharpless Oxidation Catalysts and the Conformation of Cycloalkanes Professor Barry Sharpless of Scripps Research Institute describes.

End of Lecture 34Dec. 3, 2008

Copyright © J. M. McBride 2009. Some rights reserved. Except for cited third-party materials, and frames 3-19 used by Prof. Sharpless, all content is licensed under a Creative Commons License (Attribution-NonCommercial-ShareAlike 3.0).

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The following attribution may be used when reusing material that is not identified as third-party content: J. M. McBride, Chem 125. License: Creative Commons BY-NC-SA 3.0