The Emergence of Neutral Ground-State Organic Super-Electron-Donors and their Application in Organic Synthesis Francisco J. Sarabia Literature Seminar 19 February 2015 S S S S E 0 = +0.32, +0.71 V in CH 3 CN N(CH 3 ) 2 N(CH 3 ) 2 (H 3 C) 2 N (H 3 C) 2 N E 0 = -0.78 V, -0.61 V in CH 3 CN; -0.62 V in DMF N N N N CH 3 CH 3 E 0 = -0.76 V, -0.82 V in DMF N (H 3 C) 2 N N N(CH 3 ) 2 E 0 = -1.24 V in DMF N N N N E 0 = -1.20 V in DMF N CH 3 N N (H 3 C) 2 N H 3 C N(CH 3 ) 2 H 3 C E 0 = -1.50 V in DMF Reduction potential values shown are vs SCE. TDAE TTF Neutral Ground-State Organic Electron Donors
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The Emergence of Neutral Ground-State Organic Super-Electron-Donors and their Application in
Organic Synthesis!
Francisco J. Sarabia!Literature Seminar!19 February 2015!
S
SS
S
E0 = +0.32, +0.71 V in CH3CN
N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
E0 = -0.78 V, -0.61 V in CH3CN;-0.62 V in DMF
N
N
N
N
CH3 CH3
E0 = -0.76 V, -0.82 V in DMF
N
(H3C)2N
N
N(CH3)2
E0 = -1.24 V in DMF
N
N
N
N
E0 = -1.20 V in DMF
NCH3
NN
(H3C)2N
H3C
N(CH3)2H3C
E0 = -1.50 V in DMF
Reduction potential values shown are vs SCE.
TDAETTF
Neutral Ground-State Organic Electron Donors
organic super-electron-donors (SEDs)!
Emergence!!!!Preparation!!!!Application!
Review: Broggi, J.; Terme, T.; Vanelle, P. Organic Electron Donors as Powerful Single-Electron Reducing Agents in Organic Synthesis. Angew. Chem., Int. Ed. 2014, 53, 384-413.!!Perspective: Murphy, J. A. Discovery and Development of Organic Super-Electron-Donors. J. Org. Chem. 2014, 79, 3731-3746.!
*Art by graphic artist Maxime Py and the Super-Kamiokande Collaboration!
Single Electron Transfer!-- Metals in low oxidation state (Li, Na, K) --!
!- Harsh reagents -!!!
-- Tin reagents (HSnBu3) --!!- Toxic -!
!!
-- Electrochemical reduction (metal cathode) --!!- Specific glassware, fouling of electrodes -!
!!
-- Light assisted electron transfer [photoredox catalysis (Ru, Ir)] --!!- Expensive metals* -!
!!
-- Dyes --!- High molecular weight -!
!
SET: Rowlands, G. J. Tetrahedron 2009, 65, 8603–8655. Rowlands, G. J. Tetrahedron 2010, 66, 1593–1636.!Dyes: Nicewicz, D. A.; Nguyen, T. M. ACS Catal. 2014, 4, 355-360. Fukuzumi, S.; Ohkubo, K. Org. Biomol. Chem. 2014 , 12, 6059-6071.!Photoredox Catalysis: Prier, C. K.; Rankic, D. A.; Macmillan, D. W. C. Chem. Rev. 2013, 113, 5322-5363.!Earth Abundant: Stevenson, S. M.; Shores, M. P.; Ferreira, E. M. The Development of Photooxidizing Chromium Catalysts for Promoting Radical Cation Cycloadditions, Just Submitted.!
other alternatives?!
(super) organic electron donors!
-- Neutral electron donors with ground state reducing power --!-- Highly selective and tolerant to a variety of functional groups --!
-- Soluble in organic solvents (pure organic solids or liquids) --!-- Redox potentials are tunable --!
Reduction Potential: ChemWiki: The Dynamic Chemistry E-textbook!Médebielle, M.; Dolbier, W. R. J. Flu. Chem. 2008, 129, 930-942.!Murphy, J. A. J. Org. Chem. 2014, 79, 3731-3746.
standard reduction potential: tendency for a chemical species to be reduced (measured in volts at standard conditions). The more positive the potential is the more likely it will be reduced (oxidant). The more negative the potential is the more likely it will be oxidized (reductant).!
E0 = -0.62 V in DMF
(H3C)2N
(H3C)2N N(CH3)2N(CH3)2
TDAE2+
N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
F N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
F
F
– e
SET
– e
DET
E0 = -0.78 V in CH3CN E0 = -0.61 V in CH3CN
radical cation dication
N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
E0 = -0.78 V, -0.61 V in CH3CN;-0.62 V in DMF
TDAE
TTF as organic single electron donor!
E0 = +0.37 V, +0.67 V in CH2Cl2 vs SCE!
1,3-Dithiolium Hydrogen Sulfate: E. Klingsberg, J. Am. Chem. Soc. 1964, 86, 5290-5292.!Tetrathiafulvalene: Wudl, F.; Smith, G. M.; Hufnagel, E. J. Chem. Commun. 1970, 1453-1454.!Wanzlick Equilibrium: Böhm, V. P. W.; Herrmann, W. A. Angew. Chem. Int. Ed. 2000, 39, 4036-4038.!Lampard, C.; Murphy, J. A.; Lewis, N. J. Chem. Soc., Chem. Commun. 1993, 295-297.!Fletcher, R. J.; Lampard, C.; Murphy, J. A.; Lewis, N. J. Chem. Soc., Perkin Trans 1, 1995, 623-633.!
Wanzlick-Equilibrium!
S
SS
S
SHPAA
acetone, 0.5 h, 0 ˚C
82% yieldHSO4
Et3N
S
S
S
S
CH3CN
50% yield
S
S
S
S
S
S
S
S
TTF as organic single electron donor!
1,3-Dithiolium Hydrogen Sulfate: E. Klingsberg, J. Am. Chem. Soc. 1964, 86, 5290-5292.!Tetrathiafulvalene: Wudl, F.; Smith, G. M.; Hufnagel, E. J. Chem. Commun. 1970, 1453-1454.!Lampard, C.; Murphy, J. A.; Lewis, N. J. Chem. Soc., Chem. Commun. 1993, 295-297.!Fletcher, R. J.; Lampard, C.; Murphy, J. A.; Lewis, N. J. Chem. Soc., Perkin Trans 1, 1995, 623-633.!
N2 S
SS
S
S
SS
S
+e
TTF
R R
N2
R– N2
E0 = +0.37 V, +0.67 V in CH2Cl2 vs SCE!
S
SS
S
SHPAA
acetone, 0.5 h, 0 ˚C
82% yieldHSO4
Et3N
S
S
S
S
CH3CN
50% yield
1,3-Dithiolium Hydrogen Sulfate: E. Klingsberg, J. Am. Chem. Soc. 1964, 86, 5290-5292.!Tetrathiafulvalene: Wudl, F.; Smith, G. M.; Hufnagel, E. J. Chem. Commun. 1970, 1453-1454.!Lampard, C.; Murphy, J. A.; Lewis, N. J. Chem. Soc., Chem. Commun. 1993, 295-297.!Fletcher, R. J.; Lampard, C.; Murphy, J. A.; Lewis, N. J. Chem. Soc., Perkin Trans 1, 1995, 623-633.!
TTF as organic single electron donor!
driving force: aromaticity!!
S
SS
SS
SS
S S
SS
S
– e – e
SET DET
N2 S
SS
S
S
SS
S
+e
TTF
R R
N2
R– N2
Cu(II) analogy!
Cu(II)X2
Cu(I)X
N2+e
R R
N2
R– N2
MeerweinArylaLon
Kürti, L.; Czakó, B. Strategic Applications of Named Reactions in Organic Synthesis: Background and Detailed Mechanisms. Elsevier Academic, 2005. Print.!
N2 S
SS
S
S
SS
S
+e
TTF
R R
N2
R– N2
radical-polar crossover mechanism!
Fletcher, R.; Kizil, M.; Lampard, C.; Murphy, J. A.; Roome, S. J. J. Chem. Soc., Perkin Trans. 1, 1998, 2341-2351. !Callaghan, O.; Lampard, C.; Kennedy, A. R.; Murphy, J. A. J. Chem. Soc., Perkin Trans. 1, 1999, 995-1001.!Callaghan, O.; Lampard, C.; Kennedy, A. R.; Murphy, J. A. Tet. Lett., 1999, 40, 161-164.!
NMs
N2
H–N2
NHCOCF3BF4
NMs
N2
H
NHCOCF3
NMs
H
NHCOCF3
NMs
H
NHCOCF3
NMs
H
F3COCHNS
S
S
S
NMs
H
F3COCHN
NMs
H
F3COCHNOH
NH H
N
CH3
(±) aspidospermidine
BF4
S
SS
S
S
SS
S
+e
TTF
acetone, H2O, 2 d
45% yield
TTF (1.1 equiv)-2.2%overallyield-
10stepsfromaryldiazonium
super electron donors (SEDs)!
"If a neutral organic molecule could be found that would reduce iodobenzene, we resolved to call it a "super-electron-donor" (SED)"- Prof. John A. Murphy!
Benzene: Mortensen, J.; Heinze, J. Angew. Chem. Int. Ed. Engl. 1984, 23, 84-85.!Halobenzenes: Allongue, P.; Delamar, M.; Desbat, B.; Fagebaume, O.; Hitmi, R.; Pinson, J.; Savéant, J-M. J. Am. Chem. Soc. 1997, 119, 201-207.!Aryl Diazonium Salts: Pause, L.; Robert, M.; Savéant, J-M. J. Am. Chem. Soc. 1999, 121, 7158-7159.!Alkyl Halides: Isse, A. A.; Lin, C. Y.; Coote, M. L.; Gennaro, A. J. Phys. Chem. B 2011, 115, 678-684.!Sulfone/sulfonamide: Shoenebeck, F.; Murphy, J. A.; Zhou, S.; Uenoyoma, Y.; Miclo, Y.; Tuttle, T. J. Am. Chem. Soc. 2007, 129, 13368-13369.!Murphy, J. A. J. Org. Chem. 2014, 79, 3731-3746.!
TDAE Discovery: Pruett, R. L.; Barr, J. T.; Rapp, K. E.; Bahner, C. T.; Gibson, J. D.; Lafferty, R. H., Jr. J. Am. Chem. Soc. 1950, 72, 3646-3650.!O2 reactivity: Carpenter, W.; Bens, E. M. Tetrahedron 1970, 26, 59-65.!
TDAE!
Briscoe, M. W.; Chambers, R. D.; Mullins, S. J.; Nakamura, T.; Vaughan, J. F. S.; Drakesmith, F. G. J. Chem. Soc., Perkin Trans. 1 1994, 3115-3118.!
N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
F N(CH3)2
N(CH3)2
(H3C)2N
(H3C)2N
F
F
– e
SET
– e
DET
E0 = -0.78 V, -0.61 V in CH3CN vs SCE!
F3C
F3C
CF3
CF3F
FF
F
F3C
F3C
CF3
CF3
F
F
0 ˚C to RTCH2Cl2
90% yield
TDAE
TDAE!
Briscoe, M. W.; Chambers, R. D.; Mullins, S. J.; Nakamura, T.; Vaughan, J. F. S.; Drakesmith, F. G. J. Chem. Soc., Perkin Trans. 1 1994, 3115-3118.!
Fluorine: Fluorine in Bioorganic Chemistry (Eds.: Welch, J. T.; Eswarakrishnan, S.), Wiley, New York, 1991; Bioorganic and Medicinal Chemistry of Fluorine (Eds. : Bégué, J.-P.; Bonnet-Delpon, D.), Wiley, Hoboken, 2008.!
---comparabletoTMSCF3(Ruppert-Prakashreagent)---
SiCH3
CH3F3C
H3C
Aldehydes/Ketones: Aït-Mohand, S.; Takechi, N.; Medebielle, M.; Dolbier, W. R. Org. Lett. 2001, 3, 4271-4273.!Cyclic Sulfates: Takechi, N.; Ait-Mohand, S.; Medebielle, M.; Dolbier, W. R. Org. Lett. 2002, 4, 4671-4672.!Trifluoro ethers: Pooput, C.; Medebielle, M.; Dolbier, W. R. Org. Lett. 2004, 6, 301-303.!Imines: Xu, W.; Dolbier, W. R. J. Org. Chem. 2005, 70, 4741-4745.!Imines: Pooput, C.; Dolbier, W. R.; Medebielle, M. J. Org. Chem. 2006, 71, 3564-3568.!Reagents for Fluorination. Aldrich ChemFiles 2007, 7.1, 11. Nucleophilic Trifluoromethylation.!
N(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
O
R'R
F3C
CF3R R'
HO
NR
R'SO2Tol
R
O OS
O O
CF3HO
R
CF3R
R'NHSO2Tol
RS
SR
RSe
SeR
Ar NS
Ar'
O
RS
CF3 or RSe
CF32 2
Ar NH
SAr'
OCF3
or
H
O
CF3IN(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
H
HO CF3
-35 ˚C to RT, DMF
10% yield
+ +
H
O
CF3IN(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
H
HO CF3
+ +-20 ˚C to RT,
DMF
80% yield
hυ, 12 h
TDAE + light!
charge-transfer complex (red)
N(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
I
F3C
CF3IN(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2+
hυ
Aldehydes/Ketones: Aït-Mohand, S.; Takechi, N.; Medebielle, M.; Dolbier, W. R. Org. Lett. 2001, 3, 4271-4273.!
BrBr
CO2Et CO2EtTDAEcat. I2
+THF, 67 ˚C, 6 h
97% yield
OBr
O
O
TDAE
THF, 67 ˚C, 0.5 h
94% yield
cat. I2, MgSO4
Tetrahydronapthalene: Nishiyama, Y.; Kawabata, H.; Kobayashi, A.; Nishino, T.; Sonoda, N. Tet. Lett. 2005, 46, 867-869.!1,4-diketones: Nishiyama, Y.; Kobayashi, A. Tet. Lett. 2006, 47, 5565-5567.!
*1,4-diestersalsoformedinlowyield.
diketones & esters!N(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
pharmaceutical analogs!
N
N
Cl O
O CO2H
CH3
Cl
N
N
NH
SO
O
NH2
XK469 CQS
quinoxaline anti-cancer drug candidates!
Montana, M.; Terme, T.; Vanelle, P. Tet. Lett. 2005, 46, 8373-8376.!Montana, M.; Terme, T.; Vanelle, P. Tet. Lett. 2006, 47, 6573-6576.!
N(CH3)2
(H3C)2N
(H3C)2N
N(CH3)2
H
O N
N
Br
Br
F3C
TDAE
DMF, -20 ˚C
79% yieldcis/trans
N
N
O
CF3TDAE
DMF, -20 ˚C
69% yield
N
N
O
Cl
CF3
N
N
Cl
ClCl
super electron donors (SEDs)!
"If a neutral organic molecule could be found that would reduce iodobenzene, we resolved to call it a "super-electron-donor" (SED)"- Prof. John A. Murphy!
Benzene: Mortensen, J.; Heinze, J. Angew. Chem. Int. Ed. Engl. 1984, 23, 84-85.!Halobenzenes: Allongue, P.; Delamar, M.; Desbat, B.; Fagebaume, O.; Hitmi, R.; Pinson, J.; Savéant, J-M. J. Am. Chem. Soc. 1997, 119, 201-207.!Aryl Diazonium Salts: Pause, L.; Robert, M.; Savéant, J-M. J. Am. Chem. Soc. 1999, 121, 7158-7159.!Alkyl Halides: Isse, A. A.; Lin, C. Y.; Coote, M. L.; Gennaro, A. J. Phys. Chem. B 2011, 115, 678-684.!Sulfone/sulfonamide: Shoenebeck, F.; Murphy, J. A.; Zhou, S.; Uenoyoma, Y.; Miclo, Y.; Tuttle, T. J. Am. Chem. Soc. 2007, 129, 13368-13369.!Murphy, J. A. J. Org. Chem. 2014, 79, 3731-3746.!
Ames, J. R.; Houghtaling, M. A.; Terrian, D. L.; Mitchell, T. P. Can. J. Chem. 1997, 75, 28-36.!Murphy, J. A.; Khan, T. A.; Zhou, S.; Thomson, D. W.; Mahesh, M. Angew. Chem. Int. Ed. 2005, 44, 1356-1360.!
E0 = -0.76 V, -0.82 V in DMF vs SCE!
N
N
CH3
I(CH2)3I
CH3CN, reflux, 3 d
95% yield
N
N
CH3
N
N
CH3
I I
NaH
DMF, 0 ˚C, 40 minN
N
CH3
N
N
CH3
tetraazafulvalene!
Ames, J. R.; Houghtaling, M. A.; Terrian, D. L.; Mitchell, T. P. Can. J. Chem. 1997, 75, 28-36.!Murphy, J. A.; Khan, T. A.; Zhou, S.; Thomson, D. W.; Mahesh, M. Angew. Chem. Int. Ed. 2005, 44, 1356-1360.!
E0 = -0.76 V, -0.82 V in DMF vs SCE!
I
R X R''
R'
R XR''
R'
X = O or NMsR = H or OCH3R' = H, CH3, or (CH2)3R'' = H or (CH2)3
5 examples
SED (1.2 equiv)
I
H3CO NMs
CH3
NMs
CH3
H3CO
PhCH3/DMF, 18 h, reflux
65-89% yield
PhCH3/DMF, 18 h, reflux; then, p-TSA
67% yield
H3CO
O
I
R'
R
H3CO
OR'
R
PhCH3, 15 h 110 ˚C
83-88% yield
R = H, CH3, or (CH2)3R = H or (CH2)3
3 examples
SED (1.2 equiv)
SED (1.2 equiv)
SED!
N
N
CH3
N
N
CH3
super electron donors (SEDs)!
"If a neutral organic molecule could be found that would reduce iodobenzene, we resolved to call it a "super-electron-donor" (SED)"- Prof. John A. Murphy!
Benzene: Mortensen, J.; Heinze, J. Angew. Chem. Int. Ed. Engl. 1984, 23, 84-85.!Halobenzenes: Allongue, P.; Delamar, M.; Desbat, B.; Fagebaume, O.; Hitmi, R.; Pinson, J.; Savéant, J-M. J. Am. Chem. Soc. 1997, 119, 201-207.!Aryl Diazonium Salts: Pause, L.; Robert, M.; Savéant, J-M. J. Am. Chem. Soc. 1999, 121, 7158-7159.!Alkyl Halides: Isse, A. A.; Lin, C. Y.; Coote, M. L.; Gennaro, A. J. Phys. Chem. B 2011, 115, 678-684.!Sulfone/sulfonamide: Shoenebeck, F.; Murphy, J. A.; Zhou, S.; Uenoyoma, Y.; Miclo, Y.; Tuttle, T. J. Am. Chem. Soc. 2007, 129, 13368-13369.!Murphy, J. A. J. Org. Chem. 2014, 79, 3731-3746.!
Ames, J. R.; Houghtaling, M. A.; Terrian, D. L.; Mitchell, T. P. Can. J. Chem. 1997, 75, 28-36.!Murphy, J. A.; Khan, T. A.; Zhou, S.; Thomson, D. W.; Mahesh, M. Angew. Chem., Int. Ed. 2005, 44, 1356-1360.!
I
NMs
OCH3
D
D
NMs
OCH3
NMs
OCH3+ 1e
SET
D
D2+
NMs
OCH3
NMs
+ 1e
SET (DET)
NMs
OCH3
90% yield
tetraazafulvalene 2.0!
Murphy, J. A.; Zhou, S; Schoenebeck, F. Angew. Chem. Int. Ed. Engl. 2007, 46, 5178-5183.!Ames, J. R.; Houghtaling, M. A.; Terrain, D. L.; Mitchell, T. P. Can. J. Chem. 1997, 75, 28-36.!
N
N
CH3
N
N
CH3
N
N
CH3
N
N
CH3
N
N
CH3 CH3
N
NI I
N
N
CH3 CH3
N
NI
– 1e – 1e
+ 1e + 1e
tetraazafulvalene 2.0!
Carbene: Taton, T. A.; Chen, P. Angew. Chem. Int. Ed. Engl. 1996, 33, 1011-1013.!Wanzlick Equilibrium: Böhm, V. P. W.; Herrmann, W. A. Angew. Chem. Int. Ed. 2000, 39, 4036-4038.!Murphy, J. A.; Zhou, S; Schoenebeck, F. Angew. Chem. Int. Ed. Engl. 2007, 46, 5178-5183.!Ames, J. R.; Houghtaling, M. A.; Terrain, D. L.; Mitchell, T. P. Can. J. Chem. 1997, 75, 28-36.!
Synthesis of Doubly-Bridged TAF:!
N
N
CH3
N
N
CH3
N
N
CH3
N
N
CH3
N
N
CH3 CH3
N
NI I
N
N
CH3 CH3
N
NI
– 1e – 1e
+ 1e + 1e
E0 = -1.20 V in DMF !vs SCE!
N
N
N
NI(CH2)3I
N
N
N
NI I
CH3CN, reflux, 24 d
51% yield
N
N
N
NNaH
NH3(l), reflux, 2 h
98% yield
N
N
CH3
N
N
CH3
N
N
CH3
N
N
CH3
Wanzlick-Equilibrium!
tetraazafulvalene 2.0!
Carbene: Taton, T. A.; Chen, P. Angew. Chem. Int. Ed. Engl. 1996, 33, 1011-1013.!Wanzlick Equilibrium: Böhm, V. P. W.; Herrmann, W. A. Angew. Chem. Int. Ed. 2000, 39, 4036-4038.!Murphy, J. A.; Zhou, S; Schoenebeck, F. Angew. Chem. Int. Ed. Engl. 2007, 46, 5178-5183.!Ames, J. R.; Houghtaling, M. A.; Terrain, D. L.; Mitchell, T. P. Can. J. Chem. 1997, 75, 28-36.!
Synthesis of Doubly-Bridged TAF:!
N
N
NN
NN
N
NI
II
I
E0 = -1.20 V in DMF !vs SCE!
N
N
N
NI(CH2)3I
N
N
N
NI I
CH3CN, reflux, 24 d
51% yield
N
N
N
NNaH
NH3(l), reflux, 2 h
98% yield
“it takes two to cyclize”!
N
N
N
N
N
N
N
NI I
N
N
N
NI
– 1e – 1e
+ 1e + 1e
N
N
CH3
N
N
CH3
ICO2Et
CH3CH3
DMF, 120 ˚C, 2 h
HCO2Et
CH3CH3
67% yield
Murphy, J. A.; Zhou, S.; Thomson, D. W.; Schoenebeck, F.; Mahesh, M.; Park, S. R.; Tuttle, T.; Berlouis, L. E. A. Angew. Chem. Int. Ed. Engl. 2007, 46, 5178-5183.!
E0 = -1.20 V in DMF !vs SCE!
ICO2Et
CH3CH3
HCO2Et
CH3CH3
70% yield16% yield
O
CH3
CH3DMF, RT, 2 h +
N
N
N
N
confirmation of aryl anion!
Murphy, J. A.; Zhou, S.; Thomson, D. W.; Schoenebeck, F.; Mahesh, M.; Park, S. R.; Tuttle, T.; Berlouis, L. E. A. Angew. Chem. Int. Ed. Engl. 2007, 46, 5178-5183.!
N
N
N
N
I
O
CO2EtCH3
CH3DMF, RT, 2 h
H
O
CO2EtCH3
CH3O
O
CH3
CH3
51% yield 21% yield
+
DMF, RT, 2 h
I
OCO2CH3 O
O
+
H
OCO2CH3
45% yield 49% yield
SED (1.6 equiv)
SED (1.6 equiv)
RX
X = Br, Cl
RH
DMF, 100 ˚C, 1 h
86-99% yield
SED (1.5 equiv)
reactivity of bis-sulfones!
SO2Ph
SO2Ph
R
R'H
SO2Ph
R
R'
SED
then H2O
94-98% yield
S
SO2Ph
R
R'
O
O
Ph
SO2Ph
R
R'PhSO2
CH3IPhSO2CH3
+ e+ e
SO2Ph
R
R'PhSO2
+
+
Shoenebeck, F.; Murphy, J. A.; Zhou, S.; Uenoyoma, Y.; Miclo, Y.; Tuttle, T. J. Am. Chem. Soc. 2007, 129, 13368-13369.!
N
N
N
N
Shoenebeck, F.; Murphy, J. A.; Zhou, S.; Uenoyoma, Y.; Miclo, Y.; Tuttle, T. J. Am. Chem. Soc. 2007, 129, 13368-13369.!
mono-sulfones!N
N
N
N
PhO2S
CH3H3C SED (3 equiv)
DMF, 110 ˚C, 18 h
79% yield
SED (3 equiv)
DMF, 110 ˚C, 18 h
97% yield
SED (3 equiv)
110 ˚C, 18 h
PhO2S
Ph
Ph
H3C
NRPhO2S
CH3H3C
H3C
CH3
H Ph
H3C Ph
N–S scission!
Shoenebeck, F.; Murphy, J. A.; Zhou, S.; Uenoyoma, Y.; Miclo, Y.; Tuttle, T. J. Am. Chem. Soc. 2007, 129, 13368-13369.!
NTs
NTs
Ph
SED (6 equiv)
DMF, 110 ˚C, 4 h
91% yield
SED (6 equiv)
DMF, 110 ˚C, 18 h
74% yield
SED (6 equiv)
DMF, 110 ˚C, 18 hN
Ts
NH
TsH
TsHNH
Ph
NR
+
+
N
N
N
N
in-situ SED!
N
N
CH3
N
N
CH3
N
N
CH3
N
N
CH3
WanzlickEquilibrium
N
N
CH3 CH3
N
NI I
N
N
CH3
CH3I
&
Jolly, P.I.; Zhou, S.; Thomson, D. W.; Garnier, J.; Parkinson, J. A.; Tuttle, T.; Murphy, J. A. Chem. Sci. 2012, 3, 1675-1679.!
I
N
R
MsR = H or CH3
NaH, DMF for R = HKHMDS, DMF/PhCH3 for R = CH3
N
N
CH3 CH3
N
NI I
N
R
Ms
H
N
R
Ms
R = H, 0%R = CH3, 22%
R = H, 41%R = CH3, 24%
+
N
N
CH3 CH3
N
NI I
N
N
CH3
CH3I
orI
O(CH2)3Ph
NaH, DMF
79% yield
H
O(CH2)3Ph
in-situ SED!
Jolly, P.I.; Zhou, S.; Thomson, D. W.; Garnier, J.; Parkinson, J. A.; Tuttle, T.; Murphy, J. A. Chem. Sci. 2012, 3, 1675-1679.!
N
N
CH3
CH3INaH
NH3 (l)
N
N
CH3
CH3
N
N
CH3
CH3
N
N
CH3
CH3
glass (H+ source)
N
N
CH3
CH2
N
N
CH3
CH3I
H
NaH
NH3 (l)N
N
CH3
CH2
N
N
CH3
CH3I I
Murphy, J. A.; Garnier, J.; Park, S. R.; Schoenebeck, F.; Zhou, S.; Turner, A. T. Org. Lett. 2008, 10, 1227-1230.!
DMAP derived SED!
E0 = -1.24 V in DMF vs SCE!
N
N(CH3)2
I(CH2)3I
CH3CN, reflux, 12h
91% yield
NN
N(CH3)2(H3C)2N
I INaH
NH3 (l)
83% yield
NN
N(CH3)2(H3C)2N
DMAP derived SED!
I
O CH3
CO2EtCH3
1) SED (1.5 equiv), DMF, RT
2) KOH, CH3OH, H2O50 ˚C, 12h O
CH3
CH3
O
O
CO2H
CH3
CH3
83% yield 8% yield
+
Br
O(CH2)3Ph
H
O(CH2)3Ph
SED (3 equiv)
100 ˚C, DMF
82% yield
H
96% yield from bromideRT, SED (1.5 eq)
Ht-Bu
t-Bu
t-Bu
95% yield from iodideRT, SED (1.5 eq)
PhO2S
H3C
SO2Ph
SED (3 equiv)
100 ˚C, DMF
99% yield
H3C
SO2PhH
Murphy, J. A.; Garnier, J.; Park, S. R.; Schoenebeck, F.; Zhou, S.; Turner, A. T. Org. Lett. 2008, 10, 1227-1230.!
NN
N(CH3)2(H3C)2N
CV representation!
Murphy, J. A. J. Org. Chem. 2014, 79, 3731-3746.!
N
N
N
N
CH3 CH3
N
N
N
NN
(H3C)2N
N
N(CH3)2E0 = -1.69 V
E0 values in DMF vs Fe/Fe+.
E0 = -1.65 V E0 = -1.27, -1.21 V
N–O, C–O, & S–O!
Weinreb Amides: Cutulic, S. P. Y.; Murphy, J. A.; Farwaha, H.; Zhou, S.; Chrystal, E. Synlett 2008, 2132-2136.!C–O reduction: Cutulic, S. P. Y.; Findlay, N. J.; Zhou, S.; Chrystal, E. J. T.; Murphy, J. A. J. Org. Chem. 2009, 74, 8713-8718.!S–O reduction: Jolly, P. I.; Fleary-Roberts, N.; O’Sullivan, S.; Doni, E.; Zhou, S.; Murphy, J. A. Org. Biomol. Chem. 2012, 10, 5807-5810.!