Class information for: |
Basic class information |
ID | Publications | Average number of references |
Avg. shr. active ref. in WoS |
---|---|---|---|
3684 | 1853 | 28.5 | 63% |
Classes in level above (level 2) |
ID, lev. above |
Publications | Label for level above |
---|---|---|
997 | 9937 | BIGINELLI REACTION//DIHYDROPYRIMIDINONES//MULTICOMPONENT REACTION |
Terms with highest relevance score |
Rank | Term | Type of term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|---|
1 | 1 4 DIHYDROPYRIDINES | Author keyword | 195 | 65% | 10% | 187 |
2 | 1 4 DIHYDROPYRIDINE | Author keyword | 118 | 57% | 8% | 140 |
3 | HANTZSCH 1 4 DIHYDROPYRIDINES | Author keyword | 102 | 95% | 2% | 35 |
4 | POLYHYDROQUINOLINE | Author keyword | 96 | 91% | 2% | 40 |
5 | HANTZSCH REACTION | Author keyword | 47 | 50% | 4% | 68 |
6 | POLYHYDROQUINOLINES | Author keyword | 41 | 90% | 1% | 18 |
7 | HANTZSCH CONDENSATION | Author keyword | 35 | 86% | 1% | 18 |
8 | HANTZSCH | Author keyword | 26 | 68% | 1% | 23 |
9 | 4 DIHYDROPYRIDINES | Author keyword | 23 | 74% | 1% | 17 |
10 | POLYHYDROQUINOLINE DERIVATIVES | Author keyword | 20 | 100% | 0% | 9 |
Web of Science journal categories |
Author Key Words |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
LCSH search | Wikipedia search |
---|---|---|---|---|---|---|---|
1 | 1 4 DIHYDROPYRIDINES | 195 | 65% | 10% | 187 | Search 1+4+DIHYDROPYRIDINES | Search 1+4+DIHYDROPYRIDINES |
2 | 1 4 DIHYDROPYRIDINE | 118 | 57% | 8% | 140 | Search 1+4+DIHYDROPYRIDINE | Search 1+4+DIHYDROPYRIDINE |
3 | HANTZSCH 1 4 DIHYDROPYRIDINES | 102 | 95% | 2% | 35 | Search HANTZSCH+1+4+DIHYDROPYRIDINES | Search HANTZSCH+1+4+DIHYDROPYRIDINES |
4 | POLYHYDROQUINOLINE | 96 | 91% | 2% | 40 | Search POLYHYDROQUINOLINE | Search POLYHYDROQUINOLINE |
5 | HANTZSCH REACTION | 47 | 50% | 4% | 68 | Search HANTZSCH+REACTION | Search HANTZSCH+REACTION |
6 | POLYHYDROQUINOLINES | 41 | 90% | 1% | 18 | Search POLYHYDROQUINOLINES | Search POLYHYDROQUINOLINES |
7 | HANTZSCH CONDENSATION | 35 | 86% | 1% | 18 | Search HANTZSCH+CONDENSATION | Search HANTZSCH+CONDENSATION |
8 | HANTZSCH | 26 | 68% | 1% | 23 | Search HANTZSCH | Search HANTZSCH |
9 | 4 DIHYDROPYRIDINES | 23 | 74% | 1% | 17 | Search 4+DIHYDROPYRIDINES | Search 4+DIHYDROPYRIDINES |
10 | POLYHYDROQUINOLINE DERIVATIVES | 20 | 100% | 0% | 9 | Search POLYHYDROQUINOLINE+DERIVATIVES | Search POLYHYDROQUINOLINE+DERIVATIVES |
Key Words Plus |
Rank | Web of Science journal category | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | 1 4 DIHYDROPYRIDINES | 190 | 46% | 17% | 310 |
2 | POLYHYDROQUINOLINE DERIVATIVES | 151 | 82% | 5% | 89 |
3 | HANTZSCH 1 4 DIHYDROPYRIDINES | 121 | 54% | 8% | 155 |
4 | 4 ARYL 1 4 DIHYDROPYRIDINES | 65 | 93% | 1% | 25 |
5 | DIHYDROPYRIDINES | 57 | 30% | 9% | 158 |
6 | HANTZSCH REACTION | 56 | 61% | 3% | 60 |
7 | 1 4 DIHYDROPYRIDINE DERIVATIVES | 41 | 60% | 2% | 44 |
8 | 1 3 5 TRISUBSTITUTED PYRAZOLINES | 37 | 46% | 3% | 60 |
9 | 3 COMPONENT DOMINO SYNTHESIS | 34 | 93% | 1% | 13 |
10 | DIHYDROPYRIDINE DERIVATIVES | 31 | 76% | 1% | 22 |
Journals |
Reviews |
Title | Publ. year | Cit. | Active references | % act. ref. to same field |
---|---|---|---|---|
Recent advances in new multicomponent synthesis of structurally diversified 1,4-dihydropyridines | 2012 | 47 | 74 | 43% |
Dihydropyridines: evaluation of their current and future pharmacological applications | 2009 | 69 | 69 | 52% |
1,4-DIHYDROPYRIDINES - EFFECTS OF CHIRALITY AND CONFORMATION ON THE CALCIUM-ANTAGONIST AND CALCIUM AGONIST ACTIVITIES | 1991 | 381 | 88 | 44% |
An efficient, metal-free, room temperature aromatization of Hantzsch-1,4-dihydropyridines with urea-hydrogen peroxide adduct, catalyzed by molecular iodine | 2008 | 33 | 80 | 83% |
1, 4-Dihydropyridines: A Class of Pharmacologically Important Molecules | 2014 | 4 | 33 | 48% |
Dimeric 4-Aryl-1,4-Dihydropyridines: Development of a Third Class of Nonpeptidic HIV-1 Protease Inhibitors | 2002 | 70 | 15 | 60% |
Hantzsch reaction: Recent advances in Hantzsch 1,4-dihydropyridines | 2008 | 30 | 109 | 60% |
Hantzsch-Type Dihydropyridines and Biginelli-Type Tetrahydropyrimidines: A Review of their Chemotherapeutic Activities | 2015 | 1 | 99 | 42% |
A highly efficient biomimetic aromatization of Hantzsch-1,4-dihydropyridines with t-butylhydroperoxide, catalysed by iron(III) phthalocyanine chloride | 2008 | 16 | 88 | 80% |
Fused 1,4-dihydropyridines as potential calcium modulatory compounds | 2006 | 42 | 81 | 48% |
Address terms |
Rank | Address term | Relevance score (tfidf) |
Class's shr. of term's tot. occurrences |
Shr. of publ. in class containing term |
Num. of publ. in class |
---|---|---|---|---|---|
1 | ORGAN SYNTH MOL MODELING | 12 | 86% | 0.3% | 6 |
2 | BIOLE OCHEM | 6 | 100% | 0.2% | 4 |
3 | MEMBRANE ACT CPDS BETA DIKETONES | 6 | 100% | 0.2% | 4 |
4 | ANTIRETROVIRAL THER Y | 4 | 67% | 0.2% | 4 |
5 | ANALYT CHEM MED FYSICOCHEM | 2 | 17% | 0.7% | 13 |
6 | SANKYO PHARMACOL MOLEC BIOL S | 2 | 67% | 0.1% | 2 |
7 | UCPSC | 2 | 50% | 0.2% | 3 |
8 | CAI RMN | 2 | 33% | 0.2% | 4 |
9 | BIOELE OQUIM | 1 | 18% | 0.4% | 7 |
10 | 11801 SHODAIOTANI 2 CHOME | 1 | 100% | 0.1% | 2 |
Related classes at same level (level 1) |
Rank | Relatedness score | Related classes |
---|---|---|
1 | 0.0000111576 | SILICON BETA ENAMINONES//SILICON PYRAZOLES//THERMOSENSITIVE COMPOUNDS |
2 | 0.0000099569 | MEBUDIPINE//BARNIDIPINE HYDROCHLORIDE//BARNIDIPINE |
3 | 0.0000094685 | BIGINELLI REACTION//DIHYDROPYRIMIDINONES//DIHYDROPYRIMIDINONE |
4 | 0.0000094126 | XANTHENES//XANTHENE//1 8 DIOXO OCTAHYDROXANTHENE |
5 | 0.0000073707 | NADH MODELS//NADH MODEL//NADPH MODEL |
6 | 0.0000072908 | GAMMA AND DELTA LACTONES//BISTRIMETHYLSILYLKETENE ACETALS//N ACTIVATION |
7 | 0.0000072561 | SR 33557//SR33805//H 3PN200 110 |
8 | 0.0000070132 | URAZOLES//TRIAZOLINEDIONES//BIS URAZOLES |
9 | 0.0000061686 | N PHOSPHONYL IMINES//GREEN SYNTHET CHEM FUNCT MAT//CHEM BIOMED SCI ICBMS |
10 | 0.0000060132 | CENTHAQUIN//FOSTEDIL//CAS 132031 81 3 |