formal ring-opening/cross-coupling reactions of 2-pyrones: iron-catalysed entry into stereodefined...
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Formal Ring-Opening/Cross-Coupling Reactions of 2-Pyrones: Iron-Catalysed Entry into Stereodefined Dienyl Carboxylates
Dr. Chan-Liang Sun Pr. Alois Fürstner Iron
Litterature Meeting
Maxime DauphinaisNovember 13th, 2013
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Pr. Alois Fürstner
• 2009 - 2012 Managing Director of the Max-Planck-Institut für Kohlenforschung• 1998 - Director at the MPIfK and professor at the Technical University of Dortmund• 1993 – 1998 Group leader MPIfK and lecturer at the University of Dortmund
• 1992 Habilitation in organic chemistry at the Technical University of Graz, Austria• 1990 – 1991 Post-doctoral fellow at the University of Geneva, Switzerland (Oppolzer)• 1987 – 1990 PhD at the Technical University of Graz, Austria (Weidmann)
•1962 Birth in Austria
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Pr. Alois Fürstner
24 major awards
• Arthur C. Cope Scholar Award• Mukaiyama Award• Prelog Medal
Member of boards of 15 journals
• Angewandte Chemie• Organic Syntheses• Journal of Organic Chemistry
Author of over 300 publications
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« Organometallic Chemistry »
• Alkyne Metathesis
• Alkene Metathesis
• π-Acid Catalysis
Fürstner Group
O
TBSO O
C5H11O
O
TBSO O
C5H11O
P N
Ph
Ph
O
OAu
ClAr
Ar
ArAr
MeO
MeO
Ph
E
E
E
E
H
H PhAgBF4
commercial
• Novel Concepts for Catalysis
• Total Synthesis
• Iron catalysisOTf
O O
MeMgBr
Fe(acac)3 cat.
Ru
PhPCy3
PCy3
Cl
Cl
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2-Pyrones Reactivity with Nucleophiles
1,2 – addition : Hard organometallics
Dreux, Tet. Lett. 1984, 1551.Christl, Eur. JOC 2006, 531.
O O
R-MgX
O O
RR-MgX
Y R
O OH
RY Y
1,2 – addition : L.A. Hydrides
O O
DIBAL-H
O OH
R
RR
R
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2-Pyrones Reactivity with Nucleophiles
1,4 – addition : Organocuprates
O O
CuBr-SMe2 (5 mol %)
(R,S)-Rev-Josiphos
t-BuOMe, -72 oC
O
OMgBr
hex
OMe
Ohex
H
OMeOH (5 eq.)
-72 oC to rt 66% yield94:6 er
hex-MgX
Feringa, Org. Lett. 2013, 286.
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2-Pyrones Reactivity with Nucleophiles
1,6 – addition : Cyanide and other heteroatom nucleophiles
O
O
KCN
DMF
NC
CO2H
O O
Fe(acac)3 5 mol %
Et2O / toluene, -78 oC
RMgBrR
OH
O
1,6 – addition : Grignards with Fe cat
1,6 – addition : Non-L.A. Hydrides
Vogel, Chemistry & Industry 1962, 1829.Vogel, Chemistry & Industry 1962, 268.
O
O
NaBH4
THF CO2H
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Initial Foray in Fe-Catalysed Couplings
Kharasch, JACS 1942, 2972.
“Although (Table I) no one of the metallic halides (2 to 5 mole per cent.) has any effect on the ratio of the 1,2 and 1,4 addition of methylmagnesium bromide to chalcone, yet they profoundly influence the nature of the products formed in the reaction.”
Ph Ph
O
Ph Ph
OH
Ph Ph
O
Me
MeMeMgBr
Ph
O
Ph
Ph Ph
O
no additiveCoCl2CuCl2FeCl2
0000
5906966
082721
< 20 oC
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Urabe’s Work on Acyclic Substrates
Urabe, Tet. Lett. 2004, 603.
R1
R2
COY
R3
i) ArMgBr (1.8 equiv)
FeCl2 (0.1 equiv)
THF, -30 oC, 3h
ii) E+
R1
R2
COY
R3
E
Ar
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Previous Fe Work with 2-Pyrones
O O
Fe(acac)3 5 mol %OTf
O O
R
THF / NMP, 5 min, 0 oC
R = MeMgBr 44%R = BuMgCl 37%
RMgX
Initial « Discovery »
O O
Fe(acac)3 5 mol %
HO OEt2O, -78 oC
8%11%
RMgX
O O
R = MeMgCl 79%R = C14H19MgCl 74%
OTf RR
Maulide, JOC 2010, 7962.
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Optimisation
Exclusive cis isomer requires complete absence of THF
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Accessing the Trans Isomer and Scope
• Most cis isomers > 20 : 1 (-30 oC)• Trans isomers 8-10 :1 (r.t.)
• Compatible with • primary alkyl iodides• esters• α-cyclopropanes
• Complete conversion in 20-40 min
• Methyl only?
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Limitations
• No example of secondary R-MgX
• Only E isomer accessible (>10:1)
• Works best with 3 equiv. of R-MgX
• For cis isomer, no THF solution
O O
Fe(acac)3 5 mol %
Et2O / toluene, -78 oC
84%, >10:182%, >10:1
RMgX
R = Me(CH2)5 R = Ph(CH2)3
R
OH
O
O O
Fe cat.
OH
O
MgX
R R
R R
?
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Mechanism – Acyclic System
Urabe, Tet. Lett. 2004, 603.
• expected 1,6-addition product with trans alkene
• no reaction with cis alkene
• 2-pyrone forces cis alkene
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Mechanism – pyrones
Fürstner, ACIE 2006, 440.DePuy, JACS 1977, 4070.
Standard redox cycle unlikely
OO
O
O O
O
Substrates that could not be engaged
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Sequential Couplings : Back to the Beginning
O O
Fe(acac)3 5 mol %
Et2O / toluene, -30 oC
68%, >20:1 Z84%, >20:1 Z73%, >20:1 Z
MeMgBr
R = iPr R = iBuR = (CH2)3Ph
RMe
OH
OR
O O
Fe(acac)3 5 mol %
THF / NMP, -78 oC
RMgBrOTf
78%74%60%
R = iPr R = iBuR = (CH2)3Ph
Synthesis of Fragment of Pateamine AO
O OTBSOTBSO
COOH
Fe(acac)3 5 mol %
Et2O / toluene, -60 oC
MeMgBr
80%, >10:1 Z Me2N
O
S
N
O O
OH2N
pateamine A
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Total Synthesis of Granulatamide B
Cytotoxic tryptamine derivative from Eunicella granulate
4-step synthesis from cheap commercial materials
57% overall yield
COOEt
hept Cl
O
AlCl3
CH2Cl2, reflux heptCOOEt
O
MeMgBrFe(acac)3 (5 mol%)Et2O / toluene, -30 oC80%
H2SO4,
HOAc, 40 oC
87%, 2 stepsO Ohept
hept
COOH
tryptamine, HOBt, EDC-HCl, Et3N
CH2Cl2 / DMF82%
NH
HNO
hept
Granulatamide B
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Conclusion
• 1,6-addition of Grignards to 2-pyrones complements 1,2 and 1,4-addition precedents
• Cis and trans isomers can be obtained almost exclusively by tweaking conditions
• Possible to alkylate sequentially two different positions of 2-pyrone with Grignard reagents
• One partial synthesis and one total synthesis accomplished using this methodology
O O
Fe(acac)3 5 mol %
Et2O / toluene, -78 oC
RMgBrR
OH
O
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Questions?