Azepina (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Azepina" in Italian language version.

Last modified: 07:06:36, 14 April 2025 (UTC)

Ref.Un. Ref.Website

Global rank Italian rank

2119doi.org

2^nd place

3^rd place

108elsevier.com

365^th place

327^th place

54nih.gov

5^th place

6^th place

44spectrabase.com

low place

4,284^th place

22wiley.com

150^th place

160^th place

11acs.org

865^th place

925^th place

11thieme.de

2,800^th place

low place

11eurekaselect.com

low place

7,821^st place

11beilstein-journals.org

low place

acs.org (Global: 865^th place; Italian: 925^th place)

pubs.acs.org

(EN) Attila G. Császár, Jean Demaison e Heinz Dieter Rudolph, Equilibrium Structures of Three-, Four-, Five-, Six-, and Seven-Membered Unsaturated N-Containing Heterocycles, in The Journal of Physical Chemistry A, vol. 119, n. 9, 5 marzo 2015, pp. 1731–1746, DOI:10.1021/jp5084168. URL consultato il 13 aprile 2025.

beilstein-journals.org (Global: low place; Italian: low place)

(EN) Farhan R Bou-Hamdan, François Lévesque e Alexander G O'Brien, Continuous flow photolysis of aryl azides: Preparation of 3 H -azepinones, in Beilstein Journal of Organic Chemistry, vol. 7, 17 agosto 2011, pp. 1124–1129, DOI:10.3762/bjoc.7.129. URL consultato il 13 aprile 2025.

doi.org (Global: 2^nd place; Italian: 3^rd place)

dx.doi.org

(EN) Jason A. Smith, Peter P. Molesworth e Christopher J.T. Hyland, Seven-Membered Rings, vol. 22, Elsevier, 2011, pp. 491–536, DOI:10.1016/s0959-6380(11)22016-6, ISBN 978-0-08-096685-4. URL consultato il 13 aprile 2025.
(EN) Attila G. Császár, Jean Demaison e Heinz Dieter Rudolph, Equilibrium Structures of Three-, Four-, Five-, Six-, and Seven-Membered Unsaturated N-Containing Heterocycles, in The Journal of Physical Chemistry A, vol. 119, n. 9, 5 marzo 2015, pp. 1731–1746, DOI:10.1021/jp5084168. URL consultato il 13 aprile 2025.
Jason A. Smith, Peter P. Molesworth e John H. Ryan, Chapter 7: Seven-Membered Rings, collana Progress in Heterocyclic Chemistry, vol. 21, Elsevier, 1º gennaio 2009, pp. 491–530, DOI:10.1016/s0959-6380(09)70044-3. URL consultato il 13 aprile 2025.
(EN) Manvinder Kaur, Sonali Garg e Dharambeer S. Malhi, A Review on Synthesis, Reactions and Biological Properties of Seven Membered Heterocyclic Compounds: Azepine, Azepane, Azepinone, in Current Organic Chemistry, vol. 25, n. 4, pp. 449–506, DOI:10.2174/1385272825999210104222338. URL consultato il 13 aprile 2025.
(EN) Kaddour Lamara e Robert K. Smalley, 3H-azepines and related systems. Part 4. Preparation of 3H-azepin-2-ones and 6H-azepino[2,1-b]quinazolin-12-ones by photo-induced ring expansions of aryl azides, in Tetrahedron, vol. 47, n. 12-13, 1991, pp. 2277–2290, DOI:10.1016/S0040-4020(01)96138-1. URL consultato il 13 aprile 2025.
(EN) Farhan R Bou-Hamdan, François Lévesque e Alexander G O'Brien, Continuous flow photolysis of aryl azides: Preparation of 3 H -azepinones, in Beilstein Journal of Organic Chemistry, vol. 7, 17 agosto 2011, pp. 1124–1129, DOI:10.3762/bjoc.7.129. URL consultato il 13 aprile 2025.
(DE) Hans Henning Wenk e Wolfram Sander, 2,3,5,6-Tetrafluorphenylnitren-4-yl: ein Nitrenradikal mit Quartett-Grundzustand, in Angewandte Chemie, vol. 114, n. 15, 2 agosto 2002, pp. 2873–2876, DOI:10.1002/1521-3757(20020802)114:15<2873::AID-ANGE2873>3.0.CO;2-G. URL consultato il 13 aprile 2025.
(EN) Stefan Bräse, Carmen Gil e Kerstin Knepper, Organic Azides: An Exploding Diversity of a Unique Class of Compounds, in Angewandte Chemie International Edition, vol. 44, n. 33, 19 agosto 2005, pp. 5188–5240, DOI:10.1002/anie.200400657. URL consultato il 13 aprile 2025.
Vishnu Ji Ram, Arun Sethi e Mahendra Nath, Chapter 3 - Seven-Membered Heterocycles, Elsevier, 1º gennaio 2019, pp. 393–425, DOI:10.1016/b978-0-12-819210-8.00003-5, ISBN 978-0-12-819210-8. URL consultato il 13 aprile 2025.
R. K. Smalley, 5.16 - Azepines, Pergamon, 1º gennaio 1984, pp. 491–546, DOI:10.1016/b978-008096519-2.00122-3, ISBN 978-0-08-096519-2. URL consultato il 13 aprile 2025.
Hayato Fukuda, Saki Ito e Kenji Watari, Identification of a Potent and Selective GPR4 Antagonist as a Drug Lead for the Treatment of Myocardial Infarction, in ACS Medicinal Chemistry Letters, vol. 7, n. 5, 7 marzo 2016, pp. 493–497, DOI:10.1021/acsmedchemlett.6b00014. URL consultato il 13 aprile 2025.
Harnam Singh, Nitin Gupta e Pramod Kumar, A New Industrial Process for 10-Methoxyiminostilbene: Key Intermediate for the Synthesis of Oxcarbazepine, in Organic Process Research & Development, vol. 13, n. 5, 20 agosto 2009, pp. 870–874, DOI:10.1021/op900127v. URL consultato il 13 aprile 2025.
Dmitry Tsvelikhovsky e Stephen L. Buchwald, Synthesis of Heterocycles via Pd-Ligand Controlled Cyclization of 2-Chloro-N-(2-vinyl)aniline: Preparation of Carbazoles, Indoles, Dibenzazepines, and Acridines, in Journal of the American Chemical Society, vol. 132, n. 40, 21 settembre 2010, pp. 14048–14051, DOI:10.1021/ja107511g. URL consultato il 13 aprile 2025.
(EN) David B. Kastrinsky, Jaya Sangodkar e Nilesh Zaware, Reengineered tricyclic anti-cancer agents, in Bioorganic & Medicinal Chemistry, vol. 23, n. 19, 2015-10, pp. 6528–6534, DOI:10.1016/j.bmc.2015.07.007. URL consultato il 13 aprile 2025.
(EN) Raed A. Al-Qawasmeh, Yoon Lee e Ming-Yu Cao, 11-Phenyl-[b,e]-dibenzazepine compounds: Novel antitumor agents, in Bioorganic & Medicinal Chemistry Letters, vol. 19, n. 1, 2009-01, pp. 104–107, DOI:10.1016/j.bmcl.2008.11.001. URL consultato il 13 aprile 2025.
Parisa Gholamzadeh, Chapter Three - The Pictet–Spengler Reaction: A Powerful Strategy for the Synthesis of Heterocycles, vol. 127, Academic Press, 1º gennaio 2019, pp. 153–226, DOI:10.1016/bs.aihch.2018.09.002. URL consultato il 13 aprile 2025.

doi.org

Hayato Fukuda, Saki Ito e Kenji Watari, Identification of a Potent and Selective GPR4 Antagonist as a Drug Lead for the Treatment of Myocardial Infarction, in ACS Medicinal Chemistry Letters, vol. 7, n. 5, 7 marzo 2016, pp. 493–497, DOI:10.1021/acsmedchemlett.6b00014. URL consultato il 13 aprile 2025.
Harnam Singh, Nitin Gupta e Pramod Kumar, A New Industrial Process for 10-Methoxyiminostilbene: Key Intermediate for the Synthesis of Oxcarbazepine, in Organic Process Research & Development, vol. 13, n. 5, 20 agosto 2009, pp. 870–874, DOI:10.1021/op900127v. URL consultato il 13 aprile 2025.
Dmitry Tsvelikhovsky e Stephen L. Buchwald, Synthesis of Heterocycles via Pd-Ligand Controlled Cyclization of 2-Chloro-N-(2-vinyl)aniline: Preparation of Carbazoles, Indoles, Dibenzazepines, and Acridines, in Journal of the American Chemical Society, vol. 132, n. 40, 21 settembre 2010, pp. 14048–14051, DOI:10.1021/ja107511g. URL consultato il 13 aprile 2025.

elsevier.com (Global: 365^th place; Italian: 327^th place)

linkinghub.elsevier.com

(EN) Jason A. Smith, Peter P. Molesworth e Christopher J.T. Hyland, Seven-Membered Rings, vol. 22, Elsevier, 2011, pp. 491–536, DOI:10.1016/s0959-6380(11)22016-6, ISBN 978-0-08-096685-4. URL consultato il 13 aprile 2025.
Jason A. Smith, Peter P. Molesworth e John H. Ryan, Chapter 7: Seven-Membered Rings, collana Progress in Heterocyclic Chemistry, vol. 21, Elsevier, 1º gennaio 2009, pp. 491–530, DOI:10.1016/s0959-6380(09)70044-3. URL consultato il 13 aprile 2025.
(EN) Kaddour Lamara e Robert K. Smalley, 3H-azepines and related systems. Part 4. Preparation of 3H-azepin-2-ones and 6H-azepino[2,1-b]quinazolin-12-ones by photo-induced ring expansions of aryl azides, in Tetrahedron, vol. 47, n. 12-13, 1991, pp. 2277–2290, DOI:10.1016/S0040-4020(01)96138-1. URL consultato il 13 aprile 2025.
Vishnu Ji Ram, Arun Sethi e Mahendra Nath, Chapter 3 - Seven-Membered Heterocycles, Elsevier, 1º gennaio 2019, pp. 393–425, DOI:10.1016/b978-0-12-819210-8.00003-5, ISBN 978-0-12-819210-8. URL consultato il 13 aprile 2025.
R. K. Smalley, 5.16 - Azepines, Pergamon, 1º gennaio 1984, pp. 491–546, DOI:10.1016/b978-008096519-2.00122-3, ISBN 978-0-08-096519-2. URL consultato il 13 aprile 2025.
(EN) David B. Kastrinsky, Jaya Sangodkar e Nilesh Zaware, Reengineered tricyclic anti-cancer agents, in Bioorganic & Medicinal Chemistry, vol. 23, n. 19, 2015-10, pp. 6528–6534, DOI:10.1016/j.bmc.2015.07.007. URL consultato il 13 aprile 2025.
(EN) Raed A. Al-Qawasmeh, Yoon Lee e Ming-Yu Cao, 11-Phenyl-[b,e]-dibenzazepine compounds: Novel antitumor agents, in Bioorganic & Medicinal Chemistry Letters, vol. 19, n. 1, 2009-01, pp. 104–107, DOI:10.1016/j.bmcl.2008.11.001. URL consultato il 13 aprile 2025.
Parisa Gholamzadeh, Chapter Three - The Pictet–Spengler Reaction: A Powerful Strategy for the Synthesis of Heterocycles, vol. 127, Academic Press, 1º gennaio 2019, pp. 153–226, DOI:10.1016/bs.aihch.2018.09.002. URL consultato il 13 aprile 2025.

eurekaselect.com (Global: low place; Italian: 7,821^st place)

(EN) Manvinder Kaur, Sonali Garg e Dharambeer S. Malhi, A Review on Synthesis, Reactions and Biological Properties of Seven Membered Heterocyclic Compounds: Azepine, Azepane, Azepinone, in Current Organic Chemistry, vol. 25, n. 4, pp. 449–506, DOI:10.2174/1385272825999210104222338. URL consultato il 13 aprile 2025.

nih.gov (Global: 5^th place; Italian: 6^th place)

pubchem.ncbi.nlm.nih.gov

(EN) PubChem, 1H-Azepine, su pubchem.ncbi.nlm.nih.gov. URL consultato il 13 aprile 2025.
(EN) PubChem, 2H-azepine, su pubchem.ncbi.nlm.nih.gov. URL consultato il 13 aprile 2025.
(EN) PubChem, 3H-Azepine, su pubchem.ncbi.nlm.nih.gov. URL consultato il 13 aprile 2025.
(EN) PubChem, 4H-azepine, su pubchem.ncbi.nlm.nih.gov. URL consultato il 13 aprile 2025.

spectrabase.com (Global: low place; Italian: 4,284^th place)

1H-Azepine - Optional[13C NMR] - Chemical Shifts - SpectraBase, su spectrabase.com. URL consultato il 13 aprile 2025.
(EN) 2H-AZEPINE - Optional[13C NMR] - Chemical Shifts - SpectraBase, su spectrabase.com. URL consultato il 13 aprile 2025.
3H-Azepine - Optional[13C NMR] - Chemical Shifts - SpectraBase, su spectrabase.com. URL consultato il 13 aprile 2025.
3H-Azepine - Optional[MS (GC)] - Spectrum - SpectraBase, su spectrabase.com. URL consultato il 13 aprile 2025.

thieme.de (Global: 2,800^th place; Italian: low place)

roempp.thieme.de

(DE) EBCONT Communications, Azepine, su roempp.thieme.de. URL consultato il 13 aprile 2025.

wiley.com (Global: 150^th place; Italian: 160^th place)

onlinelibrary.wiley.com

(DE) Hans Henning Wenk e Wolfram Sander, 2,3,5,6-Tetrafluorphenylnitren-4-yl: ein Nitrenradikal mit Quartett-Grundzustand, in Angewandte Chemie, vol. 114, n. 15, 2 agosto 2002, pp. 2873–2876, DOI:10.1002/1521-3757(20020802)114:15<2873::AID-ANGE2873>3.0.CO;2-G. URL consultato il 13 aprile 2025.
(EN) Stefan Bräse, Carmen Gil e Kerstin Knepper, Organic Azides: An Exploding Diversity of a Unique Class of Compounds, in Angewandte Chemie International Edition, vol. 44, n. 33, 19 agosto 2005, pp. 5188–5240, DOI:10.1002/anie.200400657. URL consultato il 13 aprile 2025.

Azepina (Italian Wikipedia)

acs.org (Global: 865th place; Italian: 925th place)

pubs.acs.org

beilstein-journals.org (Global: low place; Italian: low place)

doi.org (Global: 2nd place; Italian: 3rd place)

dx.doi.org

doi.org

elsevier.com (Global: 365th place; Italian: 327th place)

linkinghub.elsevier.com

eurekaselect.com (Global: low place; Italian: 7,821st place)

nih.gov (Global: 5th place; Italian: 6th place)

pubchem.ncbi.nlm.nih.gov

spectrabase.com (Global: low place; Italian: 4,284th place)

thieme.de (Global: 2,800th place; Italian: low place)

roempp.thieme.de

wiley.com (Global: 150th place; Italian: 160th place)

onlinelibrary.wiley.com

acs.org (Global: 865^th place; Italian: 925^th place)

doi.org (Global: 2^nd place; Italian: 3^rd place)

elsevier.com (Global: 365^th place; Italian: 327^th place)

eurekaselect.com (Global: low place; Italian: 7,821^st place)

nih.gov (Global: 5^th place; Italian: 6^th place)

spectrabase.com (Global: low place; Italian: 4,284^th place)

thieme.de (Global: 2,800^th place; Italian: low place)

wiley.com (Global: 150^th place; Italian: 160^th place)