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Chinese Chemical Letters (CCL)

Publisher :

Elsevier

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Peer reviewed only
Scopus Profile
Open Access
  • Chemistry
  • MULTIDISCIPLINARY
e-ISSN :

1878-5964

Issue Frequency :

Monthly

p-ISSN :

1001-8417

Est. Year :

1990

Mobile :

8005452522

Country :

United States

Language:

English

APC :

YES

Email :

usinfo@sciencedirect.com

Journal Descriptions

The official journal of the Chinese Chemical Society Chinese Chemical Letters (CCL) (ISSN 1001-8417) was founded in July 1990. The journal publishes preliminary accounts in the whole field of chemistry, including inorganic chemistry, organic chemistry, analytical chemistry, physical chemistry, polymer chemistry, applied chemistry, etc., satisfying a real and urgent need for the dissemination of research results, especially hot topics. The journal does not accept articles previously published or scheduled to be published. To verify originality, your article may be checked by the originality detection service CrossCheck. The types of manuscripts include the original researches and the mini-reviews. The experimental evidence necessary to support your manuscript should be supplied for the referees and eventual publication as Electronic Supplementary Information. The mini-reviews are written by leading scientists within their field and summarized recent work from a personal perspective. They cover many exciting and innovative fields and are of general interest to all chemists.


Chinese Chemical Letters (CCL) is :

International, Peer-Reviewed, Open Access, Refereed, Chemistry, MULTIDISCIPLINARY , Online or Print, Monthly Journal

UGC Approved, ISSN Approved: P-ISSN - 1001-8417, E-ISSN - 1878-5964, Established in - 1990, Impact Factor

Not Provide Crossref DOI

Indexed in PubMed

Not indexed in Scopus, WoS, DOAJ, UGC CARE

Indexing

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PubMed
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Elsevier
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Science Direct

+9 More

Publications of CCL

Research Article
  • dott image Sudhakar G Nandini Sandeep
  • dott image August, 2011

Synthesis of 5-benzylidene-3-(3-fluoro-4-yl-morpholin-4-yl-phenylimino)-thiazolidin-4-one derivatives catalyzed by [BmIm]OH and their anti-microbial a...

A series of novel 5-benzylidene-3-(3-fluoro-4-yl-morpholin-4-yl-phenylimino)thiazolidin-4-one derivatives were synthesized using [bmIm]OH as a catalyst and were tested for their antibacteria...

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