Advanced Synthetic Organic Chemistry -- 专题文献

近5年高被引文献

Site-Selective Defluorinative sp³ C–H Alkylation of Secondary Amides

article Full Text OpenAlex 165 FWCI14.776

Scalable Birch reduction with lithium and ethylenediamine in tetrahydrofuran

article Full Text OpenAlex 106 FWCI6.774

**Catalytic Chemo- and Enantioselective Transformations of gem-Diborylalkanes and (Diborylmethyl)metallic Species**

article Full Text OpenAlex 97 FWCI7.708

Late-Stage Diversification: A Motivating Force in Organic Synthesis

article Full Text OpenAlex 84 FWCI7.323

Direct Synthesis of Enamides via Electrophilic Activation of Amides

article Full Text OpenAlex 78 FWCI6.841

Stereoselective Diboration of Spirocyclobutenes: A Platform for the Synthesis of Spirocycles with Orthogonal Exit Vectors

article Full Text OpenAlex 75 FWCI6.263

Palladium-Catalyzed Markovnikov Hydroaminocarbonylation of 1,1-Disubstituted and 1,1,2-Trisubstituted Alkenes for Formation of Amides with Quaternary Carbon

article Full Text OpenAlex 73 FWCI5.059

α-Boryl Organometallic Reagents in Catalytic Asymmetric Synthesis

article Full Text OpenAlex 69 FWCI5.878

Natural Product Synthesis Enabled by Domino Processes Incorporating a 1,2-Rearrangement Step

review Full Text OpenAlex 69 FWCI1.371

Evolution in heterodonor P-N, P-S and P-O chiral ligands for preparing efficient catalysts for asymmetric catalysis. From design to applications

article Full Text OpenAlex 67 FWCI5.781

专题：Advanced Synthetic Organic Chemistry

最新文献

Recent developments in the synthesis of amidines

Synthesis and Late-stage C-H Functionalization of Papaverines

Computationally Designed Dearomative Claisen-Type Rearrangement of a Benzyl Alkynyl Ether and Cascade Reaction To Provide a Dihydroindenone

Phosphine-mediated deoxygenative synthesis of amides from carboxylic acids and N-chloro compounds

Synthesis of Amidines Via P(III)/P(V)O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides

Access to Pyrrolo- and Dihydropyrrolofuranthridones via Phosphine-Mediated MBH-Type/O-Acylation/Wittig Reaction Sequence

α-Functionalization of Pyrrolidines to Access Spirocyclic Proline Derivatives

Iridium-Photocatalyzed Difunctionalization of Alkenes Using N-Benzoyloxyamides

Total Synthesis of (+)-Cyanthiwigin U

Kinetically Controlled aza-Michael/Epimerization Cascade Enables a Scalable Total Synthesis of Putative (+)-Fumigaclavine F

近5年高被引文献

Site-Selective Defluorinative sp³ C–H Alkylation of Secondary Amides

Scalable Birch reduction with lithium and ethylenediamine in tetrahydrofuran

**Catalytic Chemo- and Enantioselective Transformations of gem-Diborylalkanes and (Diborylmethyl)metallic Species**

Late-Stage Diversification: A Motivating Force in Organic Synthesis

Direct Synthesis of Enamides via Electrophilic Activation of Amides

Stereoselective Diboration of Spirocyclobutenes: A Platform for the Synthesis of Spirocycles with Orthogonal Exit Vectors

Palladium-Catalyzed Markovnikov Hydroaminocarbonylation of 1,1-Disubstituted and 1,1,2-Trisubstituted Alkenes for Formation of Amides with Quaternary Carbon

α-Boryl Organometallic Reagents in Catalytic Asymmetric Synthesis

Natural Product Synthesis Enabled by Domino Processes Incorporating a 1,2-Rearrangement Step

Evolution in heterodonor P-N, P-S and P-O chiral ligands for preparing efficient catalysts for asymmetric catalysis. From design to applications

专题：Advanced Synthetic Organic Chemistry

最新文献

Recent developments in the synthesis of amidines

Synthesis and Late-stage C-H Functionalization of Papaverines

Computationally Designed Dearomative Claisen-Type Rearrangement of a Benzyl Alkynyl Ether and Cascade Reaction To Provide a Dihydroindenone

Phosphine-mediated deoxygenative synthesis of amides from carboxylic acids and N-chloro compounds

Synthesis of Amidines Via P(III)/P(V)O Redox Catalyzed In Situ Formation of Imidoyl Chlorides From Amides

Access to Pyrrolo- and Dihydropyrrolofuranthridones via Phosphine-Mediated MBH-Type/O-Acylation/Wittig Reaction Sequence

α-Functionalization of Pyrrolidines to Access Spirocyclic Proline Derivatives

Iridium-Photocatalyzed Difunctionalization of Alkenes Using N-Benzoyloxyamides

Total Synthesis of (+)-Cyanthiwigin U

Kinetically Controlled aza-Michael/Epimerization Cascade Enables a Scalable Total Synthesis of Putative (+)-Fumigaclavine F

近5年高被引文献

Site-Selective Defluorinative sp3 C–H Alkylation of Secondary Amides

Scalable Birch reduction with lithium and ethylenediamine in tetrahydrofuran

Catalytic Chemo- and Enantioselective Transformations of gem-Diborylalkanes and (Diborylmethyl)metallic Species

Late-Stage Diversification: A Motivating Force in Organic Synthesis

Direct Synthesis of Enamides via Electrophilic Activation of Amides

Stereoselective Diboration of Spirocyclobutenes: A Platform for the Synthesis of Spirocycles with Orthogonal Exit Vectors

Palladium-Catalyzed Markovnikov Hydroaminocarbonylation of 1,1-Disubstituted and 1,1,2-Trisubstituted Alkenes for Formation of Amides with Quaternary Carbon

α-Boryl Organometallic Reagents in Catalytic Asymmetric Synthesis

Natural Product Synthesis Enabled by Domino Processes Incorporating a 1,2-Rearrangement Step

Evolution in heterodonor P-N, P-S and P-O chiral ligands for preparing efficient catalysts for asymmetric catalysis. From design to applications

Site-Selective Defluorinative sp³ C–H Alkylation of Secondary Amides

**Catalytic Chemo- and Enantioselective Transformations of gem-Diborylalkanes and (Diborylmethyl)metallic Species**