158 related articles for article (PubMed ID: 33586990)
1. Investigations into a Stoichiometrically Equivalent Intermolecular Oxidopyrylium [5 + 2] Cycloaddition Reaction Leveraging 3-Hydroxy-4-pyrone-Based Oxidopyrylium Dimers.
Schiavone DV; Kapkayeva DM; Murelli RP
J Org Chem; 2021 Mar; 86(5):3826-3835. PubMed ID: 33586990
[TBL] [Abstract][Full Text] [Related]
2. Catalytic Enantioselective Intermolecular [5 + 2] Dipolar Cycloadditions of a 3-Hydroxy-4-pyrone-Derived Oxidopyrylium Ylide.
Fuhr KN; Hirsch DR; Murelli RP; Brenner-Moyer SE
Org Lett; 2017 Dec; 19(23):6356-6359. PubMed ID: 29148809
[TBL] [Abstract][Full Text] [Related]
3. Maltol- and Allomaltol-Derived Oxidopyrylium Ylides: Methyl Substitution Pattern Kinetically Influences [5 + 3] Dimerization versus [5 + 2] Cycloaddition Reactions.
Bejcek LP; Garimallaprabhakaran AK; Suyabatmaz DM; Greer A; Hersh WH; Greer EM; Murelli RP
J Org Chem; 2019 Nov; 84(22):14670-14678. PubMed ID: 31603325
[TBL] [Abstract][Full Text] [Related]
4. Discovery and Development of a Three-Component Oxidopyrylium [5 + 2] Cycloaddition.
D'Erasmo MP; Meck C; Lewis CA; Murelli RP
J Org Chem; 2016 May; 81(9):3744-51. PubMed ID: 27018974
[TBL] [Abstract][Full Text] [Related]
5. Intermolecular Regio- and Stereoselective Hetero-[5+2] Cycloaddition of Oxidopyrylium Ylides and Cyclic Imines.
Zhao C; Glazier DA; Yang D; Yin D; Guzei IA; Aristov MM; Liu P; Tang W
Angew Chem Int Ed Engl; 2019 Jan; 58(3):887-891. PubMed ID: 30476368
[TBL] [Abstract][Full Text] [Related]
6. 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides with Carbonyl Dipolarophiles Yielding Oxazolidine Derivatives.
Meyer AG; Ryan JH
Molecules; 2016 Jul; 21(8):. PubMed ID: 27455230
[TBL] [Abstract][Full Text] [Related]
7. Enantioselective 1,3-Dipolar (5+3) Cycloadditions of Oxidopyrylium Ylides and Vinylcyclopropanes toward 9-Oxabicyclononanes.
Gao Y; Mao Y; Miao Z
Org Lett; 2022 Apr; 24(16):3064-3068. PubMed ID: 35420826
[TBL] [Abstract][Full Text] [Related]
8. Huisgen [3 + 2] Dipolar Cycloadditions of Phthalazinium Ylides to Activated Symmetric and Non-Symmetric Alkynes.
Antoci V; Moldoveanu C; Danac R; Mangalagiu V; Zbancioc G
Molecules; 2020 Sep; 25(19):. PubMed ID: 32992961
[TBL] [Abstract][Full Text] [Related]
9. Tandem cyclization-cycloaddition behavior of rhodium carbenoids with carbonyl compounds: stereoselective studies on the construction of novel epoxy-bridged tetrahydropyranone frameworks.
Muthusamy S; Babu SA; Gunanathan C; Ganguly B; Suresh E; Dastidar P
J Org Chem; 2002 Nov; 67(23):8019-33. PubMed ID: 12423129
[TBL] [Abstract][Full Text] [Related]
10. The Synthetic Potential of Thiophenium Ylide Cycloadducts.
Pommainville A; Campeau D; Gagosz F
Angew Chem Int Ed Engl; 2022 Aug; 61(32):e202205963. PubMed ID: 35675513
[TBL] [Abstract][Full Text] [Related]
11. New Regio- and Stereoselective Cascades via Unstabilized Azomethine Ylide Cycloadditions for the Synthesis of Highly Substituted Tropane and Indolizidine Frameworks.
Chen S; Bacauanu V; Knecht T; Mercado BQ; Bergman RG; Ellman JA
J Am Chem Soc; 2016 Sep; 138(38):12664-70. PubMed ID: 27642766
[TBL] [Abstract][Full Text] [Related]
12. Highly Diastereoselective Intramolecular Asymmetric Oxidopyrylium-olefin [5 + 2] Cycloaddition and Synthesis of 8-Oxabicyclo[3.2.1]oct-3-enone Containing Ring Systems.
Ghosh AK; Yadav M
J Org Chem; 2021 Jun; 86(12):8127-8142. PubMed ID: 34015224
[TBL] [Abstract][Full Text] [Related]
13. Efficient generation of an oxidopyrylium ylide using a Pd catalyst and its [5+2] cycloadditions with several dipolarophiles.
Suga H; Iwai T; Shimizu M; Takahashi K; Toda Y
Chem Commun (Camb); 2018 Jan; 54(9):1109-1112. PubMed ID: 29333548
[TBL] [Abstract][Full Text] [Related]
14. Catalytic enantioselective intermolecular cycloaddition of 2-diazo-3,6-diketoester-derived carbonyl ylides with alkynes and styrenes using chiral dirhodium(II) carboxylates.
Shimada N; Anada M; Nakamura S; Nambu H; Tsutsui H; Hashimoto S
Org Lett; 2008 Aug; 10(16):3603-6. PubMed ID: 18616257
[TBL] [Abstract][Full Text] [Related]
15. Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis.
Narayan R; Potowski M; Jia ZJ; Antonchick AP; Waldmann H
Acc Chem Res; 2014 Apr; 47(4):1296-310. PubMed ID: 24730692
[TBL] [Abstract][Full Text] [Related]
16. Rhodium-Catalyzed (5 + 2) and (5 + 1) Cycloadditions Using 1,4-Enynes as Five-Carbon Building Blocks.
Blaszczyk SA; Glazier DA; Tang W
Acc Chem Res; 2020 Jan; 53(1):231-243. PubMed ID: 31820914
[TBL] [Abstract][Full Text] [Related]
17. Dearomative indole [5+2] cycloaddition reactions: stereoselective synthesis of highly functionalized cyclohepta[b]indoles.
Mei G; Yuan H; Gu Y; Chen W; Chung LW; Li CC
Angew Chem Int Ed Engl; 2014 Oct; 53(41):11051-5. PubMed ID: 25146238
[TBL] [Abstract][Full Text] [Related]
18. Enantioselective, Decarboxylative (3+2)-Cycloaddition of Azomethine Ylides and Chromone-3-Carboxylic Acids.
Kowalska E; Sieroń L; Albrecht A
Molecules; 2022 Oct; 27(20):. PubMed ID: 36296402
[TBL] [Abstract][Full Text] [Related]
19. Toward an understanding of the mechanisms of the intramolecular.
Domingo LR; Zaragoza RJ
J Org Chem; 2000 Sep; 65(18):5480-6. PubMed ID: 10970285
[TBL] [Abstract][Full Text] [Related]
20. Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction.
Haddad S; Boudriga S; Porzio F; Soldera A; Askri M; Knorr M; Rousselin Y; Kubicki MM; Golz C; Strohmann C
J Org Chem; 2015 Sep; 80(18):9064-75. PubMed ID: 26291879
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
