John P. Wolfe

From Wikipedia, the free encyclopedia

BornAugust 12, 1970 (age 55)

AlmamaterMIT (Ph.D.)
University of Colorado, Boulder (B.A.)

AwardsCamille Dreyfus Teacher-Scholar Award (2006)

FieldsOrganic chemistry, Organometallic chemistry, New Synthetic Methods, Catalysis, Natural Product Synthesis

John Perry Wolfe
Wolfe in 2014
Born	(1970-08-12) August 12, 1970 (age 55) Greeley, Colorado, US
Alma mater	MIT (Ph.D.) University of Colorado, Boulder (B.A.)
Awards	Camille Dreyfus Teacher-Scholar Award (2006)
Scientific career
Fields	Organic chemistry, Organometallic chemistry, New Synthetic Methods, Catalysis, Natural Product Synthesis
Institutions	Michigan (2002—) University of California, Irvine
Doctoral advisor	Stephen L. Buchwald
Other academic advisors	Larry E. Overman

John Perry Wolfe (born August 12, 1970) is an American chemist and a professor of chemistry at the University of Michigan.^[1] He is best known for palladium-catalyzed C-C and C-N bond formation reactions. He was also one of the key scientists in the development of Buchwald ligands, one of which is appropriately named "JohnPhos" after him. Wolfe has taught at the University of Michigan since 2002.

John P. Wolfe was born in Greeley, Colorado. He graduated from the University of Colorado, Boulder in 1994 with a B.A. in Chemistry. During his undergraduate career, he served as an undergraduate research assistant for Professor Gary A. Molander, focusing on the development of a SmI
₂-promoted alternative to the cyanoacetic ester synthesis.^[2]

After receiving his bachelor's degree from Colorado in 1994, he entered Massachusetts Institute of Technology (MIT), where he later earned his Ph.D. under Professor Stephen L. Buchwald in 1999 . During his five years at MIT, Wolfe co-authored 9 patents and 20 publications. Upon the completion of his Ph.D., he moved to University of California, Irvine, where he joined Professor Larry E. Overman and his research group as a National Institute of Health (NIH) National Research Service Award (NRSA) postdoctoral fellow.^[3]

In 2002, Wolfe moved to Ann Arbor, MI, where he joined the University of Michigan faculty. Since then his research has focused on numerous topics in chemistry, which altogether direct towards the development of new metal-catalyzed reactions for the synthesis of interesting, biologically active compounds.^[4] At Michigan, Wolfe is one of the most admired professors in the chemistry department for his outstanding lectures, especially in organic chemistry. The University has recognized his contributions by presenting him with teaching awards, and his students quote him as "the best professor [they]'ve had at University of Michigan", "he make[s] organic chemistry fun and not intimidating" and "words cannot express how great of a teacher and person he is".^[5]

Major contributions

Scholia has a profile for John P. Wolfe (Q18719251).

Palladium-catalyzed carboamination

John P. Wolfe has developed many palladium-catalyzed alkene carboamination reactions. These reactions contribute greatly to the synthesis of nitrogen heterocycles, which are commonly found in both pharmaceuticals and natural products.^[6]^[7]^[8] Common applications include the synthesis of pyrrolidines, and three-, five-, six- and seven-membered heterocycles such as pyrazolidines, aziridines, morpholines. His scope extends further to polycyclic heterocycles and the total synthesis of (+)-aphanorphine. These alkene aminoarylations take place via the cross-coupling of aryl or alkenyl halides with simple aminoalkene substrates to generate the heterocyclic ring with formation of a C-N bond and a C-C bond.^[9]

One area of his works focuses on the Pd(0)-catalyzed alkene aminoarylation:

Pyrrolidines can be efficiently generated via Pd(0)-catalyzed alkene aminoarylation reactions (Scheme 1). The advantages of this method are the wide substrate scope (substrates bearing N-aryl, N-acetyl, N-Boc, and N-Cbz groups) and good stereoselectivity.^[10]

The reaction is initiated by oxidative addition of the aryl bromide to Pd(0) (1), proceeded by the formation of the key intermediate palladium(aryl)amido complex 2, which then undergoes intramolecular syn-migratory insertion of the alkene into the Pd-N bond to yield 3 to generate the product via reductive elimination (Scheme 2).^[11]

Buchwald ligands

During Wolfe’s graduate career at MIT with Professor Stephen L. Buchwald, he was involved in developing dialkylbiaryl phosphine ligands (now referred to as "Buchwald ligands") that are highly efficient in palladium-catalyzed reactions. One of these ligands – JohnPhos - was named after him and is now commercially available.^[12]

In general, JohnPhos is a ligand for the Buchwald-Hartwig Cross Coupling reaction, C-X bond formation, the Heck reaction and Suzuki-Miyaura coupling.^[13] JohnPhos is a particularly effective ligand for the palladium-catalyzed amination of aryl chlorides, bromides, and triflates. The ligand allows the reactions to take place at room-temperature, and performs well for a wide range of different substrate combinations at 80-110 °C, which includes chloropyridines and functionalized aryl halides and triflates. JohnPhos is particularly useful for aminations of –neutral or electron rich aryl chlorides with a wide variety of amine coupling partners. An example of the catalytic amination of an aryl chloride with N-methylaniline at room temperature is shown in Scheme 3.^[14]

Although the high reactivity of the ligand is not completely understood, Buchwald et al. suggest some structural factors that contribute to their effectiveness: the electron rich phosphine group may help the acceleration of the oxidative addition step,^[15] the steric bulk of the ligands may accelerate the C-N bond forming reductive elimination,^[16] and the π-system of the ortho aromatic group on the ligand may participate in an interaction with the unoccupied metal d-orbital.^[17] Another hypothesis is that the metal-arene interaction could stabilize the catalyst. The arene from the aryl halide is forced to orient perpendicularly to the N-Pd bond, which should stereoelectronically favor reductive elimination.^[18]^[19]

Awards

References

↑ University of Michigan Department of Chemistry Faculty webpage; accessed 24 November 2014
↑ (a) Wolfe Research Group Website; accessed 10 November 2014 (b) CV; accessed 10 November 2014
↑ (a) Wolfe Research Group Website; accessed 10 November 2014 (b) CV; accessed 10 November 2014
↑ (a) Wolfe Research Group Website; accessed 10 November 2014
↑ “John Wolfe at University of Michigan – RateMyProfessors.com.” John Wolfe at University of Michigan – RateMyProfessors.com. RateMyProfessors.com LLC, 26 Apr. 2012. Web. 18 Nov. 2014
↑ For prior reviews, see: (a) Wolfe, J. P. Synlett 2008, 2913. (b) Wolfe, J. P. Eur. J. Org. Chem. 2007, 571. (c) Kotov, V.; Scarborough, C. C.; Stahl, S. S. Inorg. Chem. 2007, 46, 1910. (d) McDonald, R. I.; Liu, G.; Stahl, S. S. Chem. Rev. 2011, 111, 2981.
↑ For Cu-catalyzed reactions, see: (a) Chemler, S. R. Org. Biomol. Chem. 2009, 7, 3009. (b) Chemler, S. R. J. Organomet. Chem. 2011, 696, 150.
↑ For Au-catalyzed reactions, see: (a) Zhang, G.; Cui, L.; Wang, Y.; Zhang, L. J. Am. Chem. Soc. 2010, 132, 1474. (b) Brenzovich, W. E. Jr.; Benitez, D.; Lackner, A. D.; Shunatona, H. P.; Tkatchouk, E.; Goddard, W. A. III; Toste, F. D. Angew. Chem. Int. Ed. 2010, 49, 5519. (c) Mankad, N. P.; Toste, F. D. J. Am. Chem. Soc. 2010, 132, 12859. (d) Tkatchouk, E.; Mankad, N. P.; Benitez, D.; Goddard, W. A. III; Toste, F. D. J. Am. Chem. Soc. 2011, 133, 14293.
↑ "Recent Developments in Palladium-Catalyzed Alkene Aminoarylation Reactions for the Synthesis of Nitrogen Heterocycles" Danielle M. Schultz and John P. Wolfe, Synthesis 2012,44, 351-361.
↑ "Recent Developments in Palladium-Catalyzed Alkene Aminoarylation Reactions for the Synthesis of Nitrogen Heterocycles" Danielle M. Schultz and John P. Wolfe, Synthesis 2012,44, 351-361.
↑ "Recent Developments in Palladium-Catalyzed Alkene Aminoarylation Reactions for the Synthesis of Nitrogen Heterocycles" Danielle M. Schultz and John P. Wolfe, Synthesis 2012,44, 351-361.
↑ "JohnPhos." - (2-Biphenyl)di-tert-butylphosphine, 97%. Sigma Aldrich, n.d. Web. 29 Nov. 2014.
↑ "JohnPhos." - (2-Biphenyl)di-tert-butylphosphine, 97%. Sigma Aldrich, n.d. Web. 29 Nov. 2014.
↑ "A Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates." John P. Wolfe, Hiroshi Tomori, Joseph P. Sadighi, Jingjun Yin, and Stephen L. Buchwald. J. Org. Chem. 2000, 65, 1158–1174.
↑ Grushin, V. V.; Alper, H. Chem. Rev. 1994, 94, 1047-1062.
↑ (a) Hartwig, J. F.; Richards, S.; Baranano, D.; Paul, F. J. Am. Chem. Soc. 1996, 118, 3626-3633.
↑ Metal-› interactions have been observed in other palladium complexes. (a) Ossor, H.; Pfeffer, M.; Jastrzebski, J. T. B. H.; Stam, C. H. Inorg. Chem. 1987, 26, 1169-1171. (b) Falvello, L. R.; Fornies, J.; Navarro, R.; Sicilia, V.; Tomas, M. Angew. Chem. Int. Ed. Engl. 1990, 29, 891-893. (c) Sommovigo, M.; Pasquali, M.; Leoni, P.; Braga, D.; Sabatino, P. Chem. Ber. 1991, 124, 97-99. (d) Li, C.-S.; Cheng, C.-H.; Liao, F.-L.; Wang, S.-L. J. Chem. Soc., Chem. Commun. 1991, 710-712. (e) Kannan, S.; James, A. J.; Sharp, P. R. J. Am. Chem. Soc. 1998, 120, 215-216. (f) Kocˇovsky´, P.; Vyskocˇil, S.; Cı´sarˇova´, I.; Sejbal, J.; Tisˇlerova´, I.; Smrcˇina, M.; Lloyd-Jones, G. C.; Stephen, S. C.; Butts, C. P.; Murray, M.; Langer, V. J. Am. Chem. Soc. 1999, 121, 7714-7715.
↑ "A Simple, Efficient Catalyst System for the Palladium-Catalyzed Amination of Aryl Chlorides, Bromides, and Triflates." John P. Wolfe, Hiroshi Tomori, Joseph P. Sadighi, Jingjun Yin, and Stephen L. Buchwald. J. Org. Chem. 2000, 65, 1158–1174.
↑ Biaryl-forming reductive elimination from Pt(II) has been postulated to occur via a transition state in which both arenes are perpendicular to the coordination plane. See: Braterman, P. S.; Cross, R. J.; Young, G. B. J. Chem. Soc., Dalton Trans. 1977, 1892-1897.
↑ CV; accessed 10 November 2014

Authority control databases
International	VIAF WorldCat
National	United States Israel
Academics	Google Scholar
Other	Yale LUX

Palladium-catalyzed carboamination

Buchwald ligands

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