# Organic Letters

**Type:** Journals  
**Canonical URL:** https://scholariq.org/journals/organic-letters/

## Facts

| Field | Value |
| --- | --- |
| Open Access | false |
| ISSN-L | 1523-7052 |
| ISSNs | 1523-7052,1523-7060 |
| OpenAlex ID | https://openalex.org/S201989124 |
| Publisher | American Chemical Society |

## Journal papers

Showing 12 of 18.

- [In Situ Generation of Palladium Nanoparticles:  A Simple and Highly Active Protocol for Oxygen-Promoted Ligand-Free Suzuki Coupling Reaction of Aryl Chlorides](https://scholariq.org/papers/in-situ-generation-of-palladium-nanoparticles-a-simple-and-highly-active/)
- [I<sub>2</sub>/TBPB Mediated Oxidative Reaction of <i>N</i>-Tosylhydrazones with Anilines: Practical Construction of 1,4-Disubstituted 1,2,3-Triazoles under Metal-Free and Azide-Free Conditions](https://scholariq.org/papers/i-sub-2-sub-tbpb-mediated-oxidative-reaction-of-i-n-i-tosylhydrazones-with/)
- [Hofmann Rearrangement of Carboxamides Mediated by Hypervalent Iodine Species Generated in Situ from Iodobenzene and Oxone: Reaction Scope and Limitations](https://scholariq.org/papers/hofmann-rearrangement-of-carboxamides-mediated-by-hypervalent-iodine-species/)
- [Copper-Catalyzed Tandem Azide–Alkyne Cycloaddition, Ullmann Type C–N Coupling, and Intramolecular Direct Arylation](https://scholariq.org/papers/copper-catalyzed-tandem-azide-alkyne-cycloaddition-ullmann-type-c-n-coupling-and/)
- [Cross-Dehydrogenative Coupling of Strong C(sp<sup>3</sup>)–H with <i>N</i>-Heteroarenes through Visible-Light-Induced Energy Transfer](https://scholariq.org/papers/cross-dehydrogenative-coupling-of-strong-c-sp-sup-3-sup-h-with-i-n-i/)
- [Enantioselective Organocatalytic 1,6-Addition of Azlactones to <i>para</i>-Quinone Methides: An Access to α,α-Disubstituted and β,β-Diaryl-α-amino acid Esters](https://scholariq.org/papers/enantioselective-organocatalytic-1-6-addition-of-azlactones-to-i-para-i-quinone/)
- [Catalytic Asymmetric Conjugate Protosilylation and Protoborylation of 2-Trifluoromethyl Enynes for Synthesis of Functionalized Allenes](https://scholariq.org/papers/catalytic-asymmetric-conjugate-protosilylation-and-protoborylation-of-2/)
- [Design and Synthesis of Activity Probes for Glycosidases](https://scholariq.org/papers/design-and-synthesis-of-activity-probes-for-glycosidases/)
- [Oxidative Debenzylation of <i>N</i>-Benzyl Amides and <i>O</i>-Benzyl Ethers Using Alkali Metal Bromide](https://scholariq.org/papers/oxidative-debenzylation-of-i-n-i-benzyl-amides-and-i-o-i-benzyl-ethers-using/)
- [PhI(OCOCF<sub>3</sub>)<sub>2</sub>-Mediated C–C Bond Formation Concomitant with a 1,2-Aryl Shift in a Metal-Free Synthesis of 3-Arylquinolin-2-ones](https://scholariq.org/papers/phi-ococf-sub-3-sub-sub-2-sub-mediated-c-c-bond-formation-concomitant-with-a-1-2/)
- [Asymmetric Methallylation of Ketones Catalyzed by a Highly Active Organocatalyst 3,3′-F<sub>2</sub>-BINOL](https://scholariq.org/papers/asymmetric-methallylation-of-ketones-catalyzed-by-a-highly-active-organocatalyst/)
- [A Modular Approach to the Synthesis of <i>gem</i>-Disubstituted Cyclopropanes](https://scholariq.org/papers/a-modular-approach-to-the-synthesis-of-i-gem-i-disubstituted-cyclopropanes/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.