Regioselective Reductive Cross-Coupling Reaction
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1 Lit. Seminar Shinsuke Mouri (D3) Regioselective Reductive Cross-Coupling Reaction Glenn C. Micalizio obtained a Ph.D. at the University of Michigan in 2001 under the supervision of Professor William R. Roush. After postdoctoral study as a Fellow of the Helen Hay Whitney Foundation at Harvard University in the laboratory of Professor Stuart L. Schreiber, he moved to Yale University as an Assistant Professor in the Department of Chemistry (2003). In 2008, he moved to the Department of Chemistry at The Scripps Research Institute as an Associate Professor. His research is focused on the development of new synthetic methods and application of these methods to complex molecule synthesis. Contents recent review : G. C. Micalizio et.al. Eur. J. rg. Chem. 2010, Introduction (P. 1) 1. Micalizio work : Reductive Cross Coupling Reaction (P. 3) 1.1. Alkyne with Alkyne (P. 3) 1.2. Alkyne wtih Alkene (P. 5) 1.3 Allene (P.7) 1.4. Imine (P.9) 1.5. Toward complex molecule (P. 10) 2. Mecahism of Ni-caltalyzed reductive cross coupling reaction (P.13) 3. Summary and perspective (P.15) 4. Appendix (P.16) 0. Introduction difficulty in control of reactivity and regioselectivity Micalizio's strategy Ti-mediated alkoxide directed reductive cross coupling i Pr Ti R R R [Ar]3d 2 4s 2 oxidation states : +4, +3 or +2 coordiantion : 4-coordinated complex, 5 and 6 bond energy : Ti-F > Ti- > Ti-Cl > Ti-N > Ti-C (Ti-C <Zr-C) polarized Ti-C, cationic Ti reactivity of RTiL n is affected by the ligand at Ti Yukikinzokuhannouzai -handbook, Kagakudouzin (P. 93) 1/16
2 Why did Micalizio focus attention on Ti-mediated strategy? 1. The ability of Ti alkoxide to undergo rapid and reversible ligand exchange. paste mechanism of katsuki sharpless epoxidation in Strategic Applications of Named Reactions in rganic Chemistry (Kagakudouzin) 2. Cp 2 Ti-π complex are known to participate reductive cross coupling. Sharpless et. al. J. Am. Chem. Soc. 1991, 113, 106. Katuski T. et. al. rg. React. 1996,48, 1. Bercaw et. al. J. Am. Chem. Soc. 1983, 105, Sato. et. al Chem. Rev. 2000, 100, Ti alkoxide could be employed to acess similar reactivity seen with Cp 2 Ti-π comples (Kulinkovich, Sato) Kulinkovich et. al. Zh. rg. Khim. 1989, 25, the cost of stoichiometric Ti(iPr) 4 is significantly less than known catalytic systems based on Ni, Rh, Ir or Ru. 2/16
3 Alkyne + Alkyne Micalizio et. al. J. rg. Chem. 2009, 74, Class I protected alkyne gave products with moderate rr. 3/16
4 Class II Micalizio et. al. J.Am. Chem. Soc , Substrate scope is limited based on factors influencing reactivity and resioselectivity. Ti(iPr)2 Ti(iPr)4 iprmgcl Ti(iPr)2 R1 R2-78 ºC to -50 ºC 2h R1 D2 Ti(iPr)2 R2 Sato, F. et. al. Tetrahedron Lett. 1995, 36, the tetherd alkoxide plays a central role in determing regio selection. R1 D R2 D up to 100% Z :E = >99: 1 Jin Kun Cha et. al. J. Am. Chem. Soc. 1996, 118, /16
5 1.2 Alkyne with Alkene Micalizio et. al. Angew Chem , Micalizio et. al. J. Am. Chem. Soc. 2007, 129, allylic alcohol case H PMB + PMB 65% PMB PMB alkyne (1.0 equiv), ClTi(i-Pr) 3, PhMe, C 5 H 9 MgCl, -78 to -35 ºC, then recool to -78 ºC add Li-alkoxide of allylic alcohol (1.0 equiv) (-78 to 0 ºC). via formal [3,3]-rearrangement route 5/16
6 <Blank Space> 6/16
7 1.3 Allen allene+ alkyne Micalizio et. al. Chem. Commun. 2007, H Me + PMB PMB H Me 74% PMB PMB alkyne (1.4 eq.), Ti( i -Pr) 4 (2.1 eq.), c-c 5 H 9 MgCl (4.2 eq.), PhMe (-78 ºC to -30 ºC), cool to -78 ºC then add allenyl alkoxide (1 eq.), (-78 ºC to 0 ºC) allene+ imine Micalizio et. al. Synlett, 2008, 735. H i Pr + Cl n Pr N Cl n Pr NH i Pr 63%, E/Z = >20:1 Typical reaction conditions: imine (1.0 equiv), ClTi(i-Pr) 3 (1.25 equiv), c-c 5 H 9 MgCl (2.5 equiv), Et 2 (-78 ºC to -40 ºC), then add allenyl alkoxide (3-4 equiv, -40 ºC to 0 ºC). Micalizio et. al. Tetrahedron 2008, 68, /16
8 8/16
9 1.4. Imine (Micalizio et.al. Angew. Chem. Int. Ed. 2007, 46, 391.) aza-pauson Khand-like annulation reaction for the synthesis of tetrasubstituted γ-lactams (Micalizio et.al. Chem Commun. 2010, 46, 3336.) carbometalation process is irreversible. 9/16
10 Toward complex molecule Micalizio et. al. J. Am. Chem.Soc. 2008, 130, ca. 50% a) MeC(MgBr)CH2, MeC(Me)3, EtCH (cat), reflux This empirical model does not yet address the number of ligands presenton the metal center in the transition state. thers have suggested ate complexes as reactive intermediates in the Kulinkovich reaction. R R + Ti(iPr)4 nprmgbr Ti (ipr)4 R R octahedral ate complex (Micalizio et.al. J. Am. Chem. Soc. 2009, 48, 3648.) Kulinkovich et. al. Eur. J. rg. Chem. 2007, (d) Imine (2.0 equiv), Ti(i-Pr)4 (3.0 equiv), c-c5h9mgcl (6.0 equiv), 8 (1 equiv), Et2. (b) HCl(aq), THF. 10/16
11 Micalizo et. al. Nat. Chem. DI: /NCHEM.665 1)Reaction conditions for cross-coupling: vinylsilane, ClTi(i-Pr) 3, c-c 5 H 9 MgCl, Et 2 (-78 to -50 ºC), then add lithium alkoxide of vinylcyclopropane( 70 ºC to roomtemperature over 3 h). xidation conditions: TBHP, H 2, CsH.H 2, TBAF, DMF, 70 ºC. 2)xidation conditions: KF, KHC 3, H 2 2, MeH, THF. CH 2 Cl 2, Sm[Hg], THF, (85%, dr= 20:1). PDC, 4-Å molecular sieves, CH 2 Cl 2 (91%), then L-Selectride, THF (76% of desired isomer, dr=6:1). 11/16
12 (a)clti(i-pr) 3, c-c 5 H 9 MgCl, 35 (-78 to 30 ºC), PhMe, then lithium alkoxide of 34 in Et 2 (-70 ºC to room temperature over 3 h) (b)tbaf, THF (c)clti(i-pr) 3, c-c5h9mgcl, alkyne (-78 to -30 ºC), PhMe, then lithium alkoxide of the vinylcyclopropane in Et 2 (-70 ºC to room temperature over 3 h); (d) HF.pyr, CH 3 CN, CH 2 Cl 2 ; (e) PDC, DMF, H2. Yields reported are over the three-step sequence (c-e) and are adjusted based on the quantity of recovered starting material (vinylcyclopropane). Isolated yields for each reaction sequence are 38% (equation (2)), 36% (equation (3)) and 23% (equation (4)) over the three-step process (corresponding to average yields of 60-70% per step). total synthesis Micalizio et. al. J. Am. Chem. Soc. 2009, 131, Micalizio et. al. Angew. Chem. Int. Ed. 2008, 47, NH 2 H H Me Me Me Me Ac Phorbasin C Me Me H H Me Me H Me Me H N Me H Macbecin I Me 12/16
13 2. Mechanism of Ni-catalyzed reductive cross coupling reaction J. Montgomery et. al. J. Am. Chem. Soc. 2007, 129, J. Krische et. al. J. Am. Chem. Soc. 2007, 129, F. Jamison, et. al. J. Am. Chem. Soc. 2004, 126, R 1 R 2 + H R 3 Ni(0) catalyst H + /H 2 BEt 2 + BEt 3 R 1 R 3 R 2 Jamison and Houk et. al. J. Am. Chem. Soc. 2009, 131, 6654 (a) oxidative cyclization of alkyne and aldehyde to form a metallacycle intermediate, followed by transmetalation of the reductant and subsequent reductive elimination of the product (b) a similar mechanism but with the metal bonded to the reductant in the oxidative cyclization (c) oxidative addition of the reductant to the metal and subsequent insertion of the two π components (d) oxidative addition to one π component (alkyne or aldehyde) and subsequent insertion of the second component. 13/16
14 R 1 3 R 1 R 2 L Ni L L Ni R 2 4 H R 3 acetylene oxidative cyclization TS1-A Path A R 1 5 R 2 L Ni H R 3 R 1 BEt 3 L Ni R 2 R 3 6 Path B R 1 ethylene BEt 3 R 2 oxidative cyclization TB1-B L Ni H R 3 7 R 1 BEt 3 L Ni R 2 R 3 8 BEt 3 R 1 L Et Ni R 2 R 3 9 transmetalation (alkyl migration) TS2 BHEt 2 BEt 2 + R 1 R 3 R 2 11 R 1 + R 1 L Ni β-hydrogen elimination and reductive elimination TS3 R 2 H 2 R 3 R 2 10 R3 BEt /16
15 3. Summary and Perspective Micalizio demonstrated new type of reductive cross coupling based on the Ti mediated alkoxide directed strategy. This system is applicable to many type of reductive cross coupling and also Micalizio is also successful in to complex molecule. Further if possible... 1) catalytic 2) mechanism - ligand number and effect on Ti (transition state ) (Micalizio et.al. Angew. Chem. Int. Ed. 2009, 48, 3648.) 15/16
16 4. Appendix Jamison and Houk et. al. J. Am. Chem. Soc. 2010, 132, /16
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