ISSN: 0936-5214

Journal Home

Journal Guideline

Synlett Q3 Unclaimed

Georg Thieme Verlag Germany

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Synlett is a journal indexed in SJR in Organic Chemistry with an H index of 141. It has an SJR impact factor of 0,45 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,45.

Synlett focuses its scope in these topics and keywords: synthesis, catalyzed, aryl, oxidation, esters, efficient, halides, crosscoupling, approach, reaction, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Organic Chemistry (Q3)

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

0,45

SJR Impact factor

141

H Index

514

Total Docs (Last Year)

1085

Total Docs (3 years)

24731

Total Refs

1709

Total Cites (3 years)

1077

Citable Docs (3 years)

1.6

Cites/Doc (2 years)

48.11

Ref/Doc

Comments

No comments ... Be the first to comment!

Publication speed *

Review quality *

Edition and editorial team *

Institutional email or ORCID *

* The email or ORCID field is only to validate the authenticity of the comment, the identity will not be public. .

Other journals with similar parameters

Lipids Q3
Bioscience, Biotechnology and Biochemistry Q3
Tetrahedron Q3
Tetrahedron Asymmetry Q3
Organic Reactions Q3

Compare this journals

Aims and Scope

Best articles by citations

Solid Phase Synthesis of Quinoxalines

Direct Formation of Benzoins from Diarylmethanones via a Rearrangement Reaction Promoted by Samarium Metal in DMF

Enzymatic Resolution of Tropinone Derivatives

Practical Synthesis ofN-Cyclopropylanilines via Direct Condensation of Anilines with [(1-Ethoxycyclopropyl)oxy]trimethylsilane

New Applications of Camphor-Derived P,N-Ligands for Asymmetric Pd- and Ir-Catalyzed Reactions

DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) - A Nucleophillic Base

Combinatorial Synthesis of Carbohydrate Cluster on Tree-Type Linker with Orthogonally Cleavable Parts

(Diacetoxyiodo)benzene-Lithium Bromide as a Convenient Electrophilic Br+Source

Further Insight into 'Matching' of Donors and Acceptors via Reciprocal ¬?Donor Acceptor Selectivity (RDAS) Studies

Microwave-Assisted Synthesis of a-Amino Phosphonates Derived from Formylporphyrins of Natural Origin

A Novel and Convenient Approach to 2-Unsubstituted Imidazolium and Thiazolium Salts

Novel Synthesis of Fused Indoles by the Palladium-Catalyzed Cyclization ofN-Cycloalkenyl-o-haloanilines

SHOW MORE ARTICLES

Simple and Efficient Routes to Optically Activechiro- andallo-Inositol Derivatives frommyo-Inositol

Efficient Lewis Base-Catalyzed Conjugate Addition of Azide Ion to Cyclic Enones in Water

Tributyltin Hydride as a Selective Reducing Agent for Aryl Enones

Diols as Building Blocks in Solid-Phase Synthesis of Polyamine Toxins by Fukuyama-Mitsunobu Alkylation

Regio- and Stereoselective Dimerization of Terminal Alkynes to Enynes in InCl3-NaBH4-MeCN System

An Efficient Method for the Synthesis of 2,6-Branched Galacto-Oligo¬?saccharides and Its Applications to the Synthesis of Three Tetrasaccharides and a Hexasaccharide Related to the Arabinogalactans (AGs)

The Synthesis of New C2-Symmetric Chiral 1,4-Diamino Motif and Application in Catalytic Asymmetric Alkynylation of meso-Epoxides

An Efficient Acid-Catalysed 5-endo-dig Cyclisation Method for Pyrrole Synthesis

A New Biginelli Reaction Procedure Using Potassium Hydrogen Sulfate as the Promoter for an Efficient Synthesis of 3,4-Dihydropyrimidin-2(1H)-one

The Room-Temperature Palladium-Catalyzed Cyanation of Aryl Bromides and Iodides with Tri-t-butylphosphine as Ligand

New Odorless Protocols for the Synthesis of Aldehydes and Ketones from Thiol Esters

Solid-Phase Assisted N-1 Functionalization of Azamacrocycles