Detalhe da pesquisa
1.
An enzymatic Alder-ene reaction.
Nature
; 586(7827): 64-69, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32999480
2.
Cross-Electrophile Coupling of Benzyl Halides and Disulfides Catalyzed by Iron.
J Am Chem Soc
; 146(7): 4903-4912, 2024 Feb 21.
Artigo
Inglês
| MEDLINE | ID: mdl-38346333
3.
Highly Enantioselective, Hydrogen-Bond-Donor Catalyzed Additions to Oxetanes.
J Am Chem Soc
; 142(20): 9175-9180, 2020 05 20.
Artigo
Inglês
| MEDLINE | ID: mdl-32364378
4.
Enantioselective Total Syntheses of Methanoquinolizidine-Containing Akuammiline Alkaloids and Related Studies.
J Am Chem Soc
; 140(20): 6483-6492, 2018 05 23.
Artigo
Inglês
| MEDLINE | ID: mdl-29694031
5.
Arynes and Cyclic Alkynes as Synthetic Building Blocks for Stereodefined Quaternary Centers.
J Am Chem Soc
; 140(24): 7605-7610, 2018 06 20.
Artigo
Inglês
| MEDLINE | ID: mdl-29716194
6.
Understanding and Interrupting the Fischer Azaindolization Reaction.
J Am Chem Soc
; 139(42): 14833-14836, 2017 10 25.
Artigo
Inglês
| MEDLINE | ID: mdl-29022706
7.
Enantioselective Total Syntheses of Akuammiline Alkaloids (+)-Strictamine, (-)-2(S)-Cathafoline, and (-)-Aspidophylline A.
J Am Chem Soc
; 138(4): 1162-5, 2016 Feb 03.
Artigo
Inglês
| MEDLINE | ID: mdl-26783944
8.
Computational predictions of substituted benzyne and indolyne regioselectivities.
Tetrahedron Lett
; 56(23): 3511-3514, 2015 Jun 03.
Artigo
Inglês
| MEDLINE | ID: mdl-26034336
9.
Virtual Screening of a Chemically Diverse "Superscaffold" Library Enables Ligand Discovery for a Key GPCR Target.
ACS Chem Biol
; 19(4): 866-874, 2024 04 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38598723
10.
Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space.
ACS Cent Sci
; 4(12): 1727-1741, 2018 Dec 26.
Artigo
Inglês
| MEDLINE | ID: mdl-30648156
11.
Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.
Synlett
; 28(1): 1-11, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-29540961