asymmetric photochemistry liu-zhu gong group meeting september 12, 2009 wei-jun liu
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Asymmetric Photochemistry Liu-Zhu Gong Group Meeting September 12, 2009 Wei-Jun Liu. Fundemental Reaction Solid-Phase Solution-Phase Covalently-bound chiral auxilliaried Chiral complexing agents Chiral sensitizer. Review: Rau, H. Chem. Review . 1983 , 83 , 535-547. - PowerPoint PPT PresentationTRANSCRIPT
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Asymmetric PhotochemistryLiu-Zhu Gong Group Meeting
September 12, 2009
Wei-Jun Liu
1. Fundemental Reaction
2. Solid-Phase
3. Solution-Phase Covalently-bound chiral auxilliaried Chiral complexing agents Chiral sensitizer
Review: Rau, H. Chem. Review. 1983, 83, 535-547. Inoue, Y. Chem. Review. 1992, 92, 741-770. Konig, B. Chem. Review. 2006, 106, 5413-5430. Fagnoni, M. Chem. Review. 2007, 107, 2725-2756. Hoffmann, N. Chem. Review. 2008, 108, 1052-1103.
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1. Fundmental Reactions
1.1 [2+2] photocycloaddition
Synlett 2002, 1305
J. Am. Chem. Soc. 2009, 131, ASAP.
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Paternò-Büchi Reaction (between a ketone and alkene)
J. Org. Chem. 2003, 68, 9899.
J. Org. Chem. 2004, 69, 33.
Ang. Chem., Int. Ed. 2003, 42, 1642
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1.2 Photochemical Rearrangments (di-ПЛ
Synthesis 2001, 1175
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The Herteroatom Variant Photochemical Rearrangments
Ang. Chem., Int. Ed. 2002, 41, 4090
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1.3 Norrish-Yang Reaction
Synthesis 2001, 1253
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1.4 Intermolecular Addition onto Double or Triple C-C Bonds
J. Org. Chem. 2001, 66, 7320.
OOOO
O
O Ph
t-Bu
t-Bu
RCOOH R
R3R1O
R
R2R
PhCH3PhCH2
OH OH
O O O
O
O O
O
ON N
PhN OMe
O
SiMe3Et
PhN OMe
O
EtH2N O
H
H2N O
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1.5 Photo-oxygenation
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Why Study Asymmetric Photochemistry?
Prebiotic photochemistry ---- enantiomeric excess of biomolecules may have been generated by circularly polarized light (CPL)
Environmentally benign processes ---- light is ubiquitous, generates no waste.
Different mode of reactivity ---- access to novel, strained compounds which are thermally inaccessible or diffcult to synthesize and low reaction temperature
Short excited lifetime
low activation energy for reactions in excited states
Why few Examples in Enantioselective Photochemical Transformations
A few energy difference of a few kilocalories per mole is sufficient to give >99% stereodifferentiation.
Inoue, Y. Chem. Review. 1992, 92, 741-770.
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2. Enantioselective Solid-Phase Photochemistry2.1 Host-Gest Cocrystals
Toda, Chem. Comm. 1995, 621
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100% ee Toda, Tanaka ACIE, 1999, 38, 3523
91-99.5% ee Tanaka OL, 2002, 4, 3255
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2.2 Ionic Chiral Auxiliary
Scheffer ACR, 1996, 29, 203
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2.3 Chiral Modified Supercages of Zeolites
Ramamurthy ACR, 2003, 36, 509
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3. Enantioselective Solution-Phase Photochemistry
3.1 Covalently-bound chiral auxillaries
Meyer, JACS, 1986, 108, 306
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Carreira, JACS, 1994, 116, 6622 JACS, 1997, 119, 2597
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3.2 Chiral Complexing Agents (Templated Photochemsitry)
3.2.1 Noncovalent Asseemblies
EJOC, 2002, 2298
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JOC, 1995, 60, 7984
Glycol-Metal Cation
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Diaminotriazine-barbiturate(二氨基三唑-巴比妥酸盐)
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CR, 2006, 106, 5413-5430
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3.2.2 Complementary DNA Strands as Templates
CR, 2006, 106, 5413-5430
T
DNA RNA
A
G
C
U
A
G
C
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3.2.3 Templates with a Covalently Bound Chromophore and Recognition Site
• The reaction did not proceed in the absence of the template
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• As an artificial functional model of a photolyase
CR, 2006, 106, 5413-5430
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3.2.4 Photochemical reaction in a molecular flask
The molecular flask is significantly larger than the guest and can therefore protect Substrates from the surrounding environment and thus controls the course of a Photochemical reaction.
• The syn isomers were the major.• The syn isomers changed to the minor.
Favorite temperate scaffolds Good availability Various sizes Inherent chirality CR, 2006, 106, 5413-5430
Cyclodextrin
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Self-Assembled Molecular Cage
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3.2.5 Templates Containing a Shield
Mori and Nakamura, TL, 1996, 37, 8523-8526
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dr: 95/5yield: 56%
Bach, T. JACS, 1999, 121, 10650-10651
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Bach, T. ACIE, 2000, 39, 2302-2304
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dr: up to 95/5ee: up to 98
Bach, T. JACS, 2000, 122, 11525-11526
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dr: up to 95/5ee: up to 97
Bach, T. ACIE, 2003, 42, 3693-3696
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Bach, T. OL, 2001, 3, 601-603
Bach, T. CC, 2001, 607Bach, T. CEJ, 2002, 8, 2464
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Catalytic Enantioselective Photochemical Reaction
Krische, J. JOC, 2003, 68, 15-21
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Bach, T. Nature, 2005, 436, 1139-1140
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Bach, T. ACIE, 2009, 48, 1-4
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dr: up to 96/4ee: up to 99%
Polymer-Bound Chiral Temple
Bach, T. ACIE, 2008, 47, 7957-7959
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3.3 Chiral Sensitizer
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Inoue JCS CC, 1993, 718
Schuster, JACS, 1990, 112, 9635
Photosensitized ant-Markovnikov methanol additiong to 1,1-diphenylpropene
[4+2] cycloaddition between electron-rich diene and electron-rich dienophile
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Sens* 2b : up to 70% ee
• Switching the product chiralty by solvent• lower temperature higher ee • The higheat ee ever reported for an enantiodifferentiating photosensitization.
Inoue, JACS, 2000, 122, 406-407
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HO
O
O
O
O
O
hv (>300 nm)
7% ee
N
Ph
Ph Ph
BF4
Sens*
Garcia, JOC, 2002, 67, 5184-5189
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3.3 Activation of Substates by Chiral Catalysts (Organocatalysis)
R
O NH
COOHN
R
COOH
3O2
1O2
hv, TPP
OPh Ph
Ph
BF4
N
R
COO
HOO
O
R
HOONaBH4OH
R
HO
R
Yield
ee
CH2Ph i-Pr n-Pent n-Bu
77% 75% 77% 73%
66% 57% 54% 57%
ONH2
O
OH
20%O
HO
87% yield, 56% ee Cordova, JACS, 2004, 126, 8914 ACIE, 2004, 43, 6532
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O
H
YBr
R
FG
fluorenscent light
organocatalyst
Ru(bpy)3Cl2
H
O
FG
Y
R
MacMillan Science, 2008, 322, 77JACS, 2009, 131, 10875
N N
BPY
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4 Photecatalysts
A: Via electron transfer
O
O
Cl Cl
Cl Cl
Chloranil
CO2Me
CO2Me
DMT
NC
NC CN
CN
TCB
CN
CN
DCB
O
Ph
Ph Ph
BF4
TPP
CN
CN
DCN
O
O
Anthraquinone
CN
CN
DCA
MeO2C
MeO2C CO2Me
CO2Me
TMPM
O
BP
OMe
OMe
DMN
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B: Via H abstraction
O
NaO3S SO3Na
BPSS
O
BP
O O
UO22+ (Uranyl) (Bu4N)4W10O32 (TBADT)
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5. Conclusion
Solid-Phase asymmetric photochemistry can work very well, but has limited.
Solution-phase photochemistry is more attractive for the catalytic enantiosele-ctive photochemistry. More excellent catalysts as Bach’ catalysts and assymme-tric inducing model will be developed.
Asymmetric photochemistry using chiral sensitizers is usually poorly selective.