Detalhe da pesquisa
1.
Copper-catalyzed room-temperature cross-dehydrogenative coupling of secondary amides with terminal alkynes: a chemoselective synthesis of ynamides.
Org Biomol Chem
; 22(6): 1299-1309, 2024 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38259138
2.
One-Pot Synthesis of α-Amino Bisphosphonates from Nitriles via Tf2O/HC(OR)3-Mediated Interrupted Ritter-Type Reaction.
J Org Chem
; 87(14): 9044-9055, 2022 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35748643
3.
Tf2O-Mediated Cyclization of 7-Enamides: Bioinspired Construction of Fused Eight-Membered Carbocyclic Enimines and Enones.
J Org Chem
; 86(23): 16926-16939, 2021 12 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34752091
4.
Tf2O/TTBP (2,4,6-Tri-tert-butylpyrimidine): An Alternative Amide Activation System for the Direct Transformations of Both Tertiary and Secondary Amides.
J Org Chem
; 86(23): 16300-16314, 2021 12 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34499513
5.
Synthesis of Functionalized Bicyclo[2.2.2]octan-2-ones Skeleton via Tandem Process of Amino Acid Involved Formal [4 + 2] and Decarboxylative-Mannich Sequence.
J Org Chem
; 86(4): 3276-3286, 2021 02 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-33530688
6.
Double Addition of Alkynyllithium Reagents to Amides/Lactams: A Direct and Flexible Synthesis of 3-Amino-1,4-diynes Bearing an Aza-Quaternary Carbon Center.
J Org Chem
; 84(14): 9270-9281, 2019 07 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31287315
7.
Versatile One-Pot Synthesis of Polysubstituted Cyclopent-2-enimines from α,ß-Unsaturated Amides: Imino-Nazarov Reaction.
Angew Chem Int Ed Engl
; 57(32): 10352-10356, 2018 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29924902
8.
Organocatalytic, Asymmetric Total Synthesis of (-)-Halicloninâ A.
Angew Chem Int Ed Engl
; 55(12): 4064-8, 2016 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-26890255
9.
Radical migration-addition of N-tert-butanesulfinyl imines with organozinc reagents.
J Org Chem
; 78(22): 11229-37, 2013 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24160561
10.
Total synthesis of (-)-sessilifoliamide J.
J Org Chem
; 78(1): 35-41, 2013 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-22946828
11.
1-Benzyl-5-ethyl-5-hy-droxy-1H-pyrrol-2(5H)-one.
Acta Crystallogr Sect E Struct Rep Online
; 69(Pt 7): o1136, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24046687
12.
Reductive hydroxyalkylation/alkylation of amines with lactones/esters.
Org Biomol Chem
; 10(32): 6504-11, 2012 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-22752071
13.
A flexible asymmetric approach to methyl 5-alkyltetramates and its application in the synthesis of cytotoxic marine natural product belamideâ A.
Chemistry
; 17(3): 958-68, 2011 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-21226113
14.
Asymmetric synthesis of the cytotoxic marine natural product (+)-awajanomycin and its C-11 epimer.
J Org Chem
; 75(12): 4230-43, 2010 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-20507081
15.
A flexible approach for the asymmetric syntheses of hyacinthacines A2, A3 and structural confirmation of hyacinthacine A3.
Org Biomol Chem
; 8(9): 2085-91, 2010 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20401385
16.
4-Bromo-2-chloro-aniline.
Acta Crystallogr Sect E Struct Rep Online
; 66(Pt 1): o250, 2009 Dec 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21580132
17.
Organocatalytic, Enantioselective Reductive Bis-functionalization of Secondary Amides: One-Pot Construction of Chiral 2,2-Disubstituted 3-Iminoindoline.
Org Lett
; 21(18): 7587-7591, 2019 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31479277
18.
Divergent synthesis of N-heterocyclic 1,6-enynes through a zinc-catalyzed decarboxylative A3 reaction.
Chem Commun (Camb)
; 55(94): 14170-14173, 2019 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31701971
19.
(3S,7aR)-7-Meth-oxy-7a-methyl-3-phenyl-2,3-dihydro-pyrrolo[2,1-b]oxazol-5(7aH)-one.
Acta Crystallogr Sect E Struct Rep Online
; 65(Pt 1): o27, 2008 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-21581670
20.
Asymmetric Total Synthesis and Absolute Configuration Determination of (-)-Verrupyrroloindoline.
Org Lett
; 20(14): 4200-4203, 2018 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29969900