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ISSN: 1875-6255 (Online)
ISSN: 1570-1786 (Print)
Volume 15, 12 Issues, 2018
Download PDF Flyer
Letters in Organic Chemistry
This journal supports open access
Impact Factor:
0.73
5 - Year Impact Factor:
0.691
Aims & Scope
Abstracted/Indexed in
Submit Manuscripts Online
Editor-in-Chief:
Alberto Marra
University of Montpellier
Montpellier
France
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ISSN: 1875-6255 (Online)
ISSN: 1570-1786 (Print)
Volume 15, 12 Issues, 2018
Download PDF Flyer
Letters in Organic Chemistry
This journal supports open access
Impact Factor:
0.73
5 - Year Impact Factor:
0.691
Aims & Scope
Abstracted/Indexed in
Submit Manuscripts Online
Editor-in-Chief:
Alberto Marra
University of Montpellier
Montpellier
France
View Full Editorial Board
Subscribe
Purchase Articles
Order Reprints
Journal Home
Editorial Policies
Publishing Ethics
Self-Archiving Policies
Reviewer Guidelines
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Free Copies Online
Contents & Abstracts
Open Access Articles
Most Accessed Articles
Most Cited Articles
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More Options
Special Issue Submission
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Letters in Organic Chemistry
This journal supports open access
Quick Links
Journal Home
Editorial Policies
Publishing Ethics
Self-Archiving Policies
Reviewer Guidelines
Instructions for Authors
Free Copies Online
Contents & Abstracts
Open Access Articles
Most Accessed Articles
Most Cited Articles
Advertise With Us
Library Recommendation
Trial Requests
Special Issue Submission
Open Access Funding
Impact Factor:
0.73
5 - Year Impact Factor:
0.691
Aims & Scope
Abstracted/Indexed in
Submit Manuscripts Online
Editor-in-Chief:
Alberto Marra
University of Montpellier
Montpellier
France
View Full Editorial Board
Subscribe
More Options
Purchase Articles
Order Reprints
Contents
Letters in Organic Chemistry
,
Volume 10
- Number 10
Graphical Abstracts
,
10
(
10
):
i
- iv
DOI:
10.2174/157017861010131126115102
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1,2,4-Triazoles: A Review of Synthetic Approaches and the Biological Activity
,
10
(
10
):
693
- 714
Suresh Maddila, Ramakanth Pagadala and Sreekanth B. Jonnalagadda
DOI:
10.2174/157017861010131126115448
View Abstract
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View Abstract
An Efficient Synthesis of Some New Hydrazone Derivatives Containing 1,2,3-Triazole and Thiazole
,
10
(
10
):
715
- 721
Keyume Ablajan, Wang Liju and Anagu Tuoheti
DOI:
10.2174/157017861010131126115715
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Tungstate Sulfuric Acid (TSA): A Green and Highly Efficient Catalyst for Novel and Known Polysubstituted Imidazoles Synthesis
,
10
(
10
):
722
- 732
Bahador Karami, Khalil Eskandari and Mahboobeh Azizi
DOI:
10.2174/15701786113109990044
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View Abstract
Efficient Synthesis of 6-O-methyl-scutellarein from Scutellarin via Selective Methylation
,
10
(
10
):
733
- 737
Min-Zhe Shen, Zhi-Hao Shi, Nian-Guang Li, Hao -Tang, Qian-Ping Shi, Yu-Ping Tang, Jian-Ping Yang and Jin-Ao Duan
DOI:
10.2174/15701786113109990046
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Green and Facile Synthesis of 1,4-Disubstituted 1,2,3-Triazoles via a Click Reaction of α-Bromo Ketones, [bmim]N
3
and Terminal Acetylenes
,
10
(
10
):
738
- 743
Azadeh Fazeli, Hossein A. Oskooie, Yahya S. Beheshtiha, Majid M. Heravi and Hassan Valizadeh
DOI:
10.2174/15701786113109990036
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Efficient Green Synthesis of Bis(3-indolyl)phenylmethanes Catalyzed by 1- (Benzenesulfonyl)-3-methyl-1H-imidazolium Chlorides
,
10
(
10
):
744
- 751
Gantigaiah Krishnamurthy and Kesturu Venkatarayappa Jagannath
DOI:
10.2174/157017861010131126121040
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Novel 1,2,3-Triazole-Bisphenol-Based Macrocycle Synthesized Through Click Chemistry
,
10
(
10
):
752
- 757
Burhan Khan, Said Nadeem, Muhammad R. Shah, Sammer Yousuf and Numan Hoda
DOI:
10.2174/15701786113109990040
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Copper- and Solvent-free Sonogashira Reaction Catalyzed by Polyvinyl Chloride-supported Palladium(II) Triazole Complex
,
10
(
10
):
758
- 763
Mohammad Bakherad, Ali Keivanloo, Bahram Bahramian and Maesoume Siavoshi
DOI:
10.2174/15701786113109990048
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Green and Highly Efficient One-Pot Synthesis of Some New Bis Thiazolidinones
,
10
(
10
):
764
- 769
Akbar Mobinikhaledi and Alireza Khajeh Amiri
DOI:
10.2174/157017861131000059
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Synthesis of Methylenebisamides by TFA-Promoted Reactions of Nitriles and DMSO
,
10
(
10
):
770
- 773
Lingxia Pan, Lin Huang and Chunsong Xie
DOI:
10.2174/15701786113109990049
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Acknowledgements to the Reviewers
,
10
(
10
):
774
DOI:
10.2174/157017861010131126125021
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