Zobrazeno 1 - 10
of 487
pro vyhledávání: '"Brian M. Stoltz"'
Publikováno v:
Catalysts, Vol 13, Iss 9, p 1258 (2023)
We explore the origins of the marked improvement in enantioselectivity in the inner-sphere (PHOX)Pd-catalyzed allylic alkylation of N-benzoyl lactam nucleophiles over their carbocyclic counterparts. We employ density functional theory calculations to
Externí odkaz:
https://doaj.org/article/82f1e14634ab4afa86871ee073d67f7d
Autor:
Christopher G. Jones, Matthew Asay, Lee Joon Kim, Jack F. Kleinsasser, Ambarneil Saha, Tyler J. Fulton, Kevin R. Berkley, Duilio Cascio, Andrey G. Malyutin, Matthew P. Conley, Brian M. Stoltz, Vincent Lavallo, José A. Rodríguez, Hosea M. Nelson
Publikováno v:
ACS Central Science, Vol 5, Iss 9, Pp 1507-1513 (2019)
Externí odkaz:
https://doaj.org/article/4a58587728b347ca958df93828a40b03
Autor:
Christopher G. Jones, Michael W. Martynowycz, Johan Hattne, Tyler J. Fulton, Brian M. Stoltz, Jose A. Rodriguez, Hosea M. Nelson, Tamir Gonen
Publikováno v:
ACS Central Science, Vol 4, Iss 11, Pp 1587-1592 (2018)
Externí odkaz:
https://doaj.org/article/804f116afbda4e23b71f6e32e189a3b1
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2038-2045 (2016)
An enantioconvergent catalytic process has the potential to convert a racemic starting material to a single highly enantioenriched product with a maximum yield of 100%. Three mechanistically distinct approaches to effecting enantioconvergent catalysi
Externí odkaz:
https://doaj.org/article/05f0fbec54bf4cceb0823eeed12f3fc6
Autor:
Yiyang Liu, Marc Liniger, Ryan M. McFadden, Jenny L. Roizen, Jacquie Malette, Corey M. Reeves, Douglas C. Behenna, Masaki Seto, Jimin Kim, Justin T. Mohr, Scott C. Virgil, Brian M. Stoltz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2501-2512 (2014)
Pd-catalyzed enantioselective alkylation in conjunction with further synthetic elaboration enables the formal total syntheses of a number of “classic” natural product target molecules. This publication highlights recent methods for setting quater
Externí odkaz:
https://doaj.org/article/53aff6b2b8524eb8bcb18875eaef6ba1
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1637-1642 (2013)
An efficient method for the synthesis of the (S)-4-(tert-butyl)-2-(pyridin-2-yl)-4,5-dihydrooxazole ((S)-t-BuPyOx) ligand has been developed. Inconsistent yields and tedious purification in known routes to (S)-t-BuPyOx suggested the need for an effic
Externí odkaz:
https://doaj.org/article/bd8d3f9a94174a84bc87c3d67ff418eb
Autor:
Kaylin N. Flesch, Alexander Q. Cusumano, Peng-Jui Chen, Christian Santiago Strong, Stephen R. Sardini, Yun E. Du, Michael D. Bartberger, William A. Goddard, Brian M. Stoltz
Publikováno v:
Journal of the American Chemical Society. 145:11301-11310
Publikováno v:
Journal of the American Chemical Society. 145:7763-7767
Autor:
Alexander W. Rand, Kevin J. Gonzalez, Christopher E. Reimann, Scott C. Virgil, Brian M. Stoltz
Publikováno v:
Journal of the American Chemical Society. 145:7278-7287
Autor:
Nicholas J. Hafeman, Steven A. Loskot, Christopher E. Reimann, Beau P. Pritchett, Scott C. Virgil, Brian M. Stoltz
Publikováno v:
Chemical Science. 14:4745-4758
The complete account of the total syntheses of scabrolide A and yonarolide is disclosed. This article describes an initial approach involving a bio-inspired macrocyclization/transannular Diels–Alder cascade, which ultimately failed due to undesired