Нонены (Russian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Нонены" in Russian language version.

Last modified: 04:00:00, 6 May 2026 (UTC)

Ref.Un. Ref.Website

Global rank Russian rank

1110doi.org

2^nd place

5^th place

87worldcat.org

4^th place

3^rd place

44acs.org

865^th place

1,368^th place

41dguv.de

690^th place

7,541^st place

33nist.gov

708^th place

1,056^th place

32chemicalbook.com

9,407^th place

low place

33springer.com

182^nd place

283^rd place

22wiley.com

150^th place

194^th place

21sciencedirect.com

137^th place

197^th place

11elsevier.com

365^th place

501^st place

11wanfangdata.com.cn

7,189^th place

low place

11web.archive.org

1^st place

11sigmaaldrich.com

774^th place

4,907^th place

11nih.gov

5^th place

11^th place

acs.org (Global: 865^th place; Russian: 1,368^th place)

pubs.acs.org

Frank C. Whitmore, L. W. Mixon. Polymerization of Olefins. IV. 1 The Nonenes from the Dehydration and Copolymerization of t-Butyl and t-Amyl Alcohols 2 (англ.) // Journal of the American Chemical Society. — 1941-05. — Vol. 63, iss. 5. — P. 1460–1462. — ISSN 0002-7863. — doi:10.1021/ja01850a092.
George C. Johnson, Frank S. Fawcett. Inter-polymerization of Isobutene and 2-Methyl-2-butene Using an Alumina-Silica Catalyst. Composition of the Hydrogenated Nonenes (англ.) // Journal of the American Chemical Society. — 1946-08. — Vol. 68, iss. 8. — P. 1416–1419. — ISSN 0002-7863. — doi:10.1021/ja01212a005.
Frank C. Whitmore, E. E. Stahly. The Common Basis of Intramolecular Rearrangements. II. 1 The Dehydration of Di-tert-butylcarbinol and the Conversion of the Resulting Nonenes to Trimethylethylene and Isobutylene (англ.) // Journal of the American Chemical Society. — 1933-10. — Vol. 55, iss. 10. — P. 4153–4157. — ISSN 0002-7863. — doi:10.1021/ja01337a042.
R. A. Benkeser, F. G. Belmonte. Reduction of alkynes by a new reducing system (англ.) // The Journal of Organic Chemistry. — 1984-05. — Vol. 49, iss. 9. — P. 1662–1664. — ISSN 0022-3263. — doi:10.1021/jo00183a038.

chemicalbook.com (Global: 9,407^th place; Russian: low place)

TRANS-2-NONENE price,buy TRANS-2-NONENE - chemicalbook . www.chemicalbook.com. Дата обращения: 6 марта 2026.
CIS-2-NONENE | 6434-77-1 (англ.). ChemicalBook. Дата обращения: 6 марта 2026.

dguv.de (Global: 690^th place; Russian: 7,541^st place)

gestis.dguv.de

Record of 1-Nonen in the GESTIS Substance Database of the IFA, accessed on 1 February 2016

doi.org (Global: 2^nd place; Russian: 5^th place)

dx.doi.org

Johan A. Martens, Wim H. Verrelst, Georges M. Mathys, Stephen H. Brown, Pierre A. Jacobs. Tailored Catalytic Propene Trimerization over Acidic Zeolites with Tubular Pores (англ.) // Angewandte Chemie International Edition. — 2005-09-05. — Vol. 44, iss. 35. — P. 5687–5690. — ISSN 1433-7851. — doi:10.1002/anie.200463045.
Frank C. Whitmore, L. W. Mixon. Polymerization of Olefins. IV. 1 The Nonenes from the Dehydration and Copolymerization of t-Butyl and t-Amyl Alcohols 2 (англ.) // Journal of the American Chemical Society. — 1941-05. — Vol. 63, iss. 5. — P. 1460–1462. — ISSN 0002-7863. — doi:10.1021/ja01850a092.
George C. Johnson, Frank S. Fawcett. Inter-polymerization of Isobutene and 2-Methyl-2-butene Using an Alumina-Silica Catalyst. Composition of the Hydrogenated Nonenes (англ.) // Journal of the American Chemical Society. — 1946-08. — Vol. 68, iss. 8. — P. 1416–1419. — ISSN 0002-7863. — doi:10.1021/ja01212a005.
Frank C. Whitmore, E. E. Stahly. The Common Basis of Intramolecular Rearrangements. II. 1 The Dehydration of Di-tert-butylcarbinol and the Conversion of the Resulting Nonenes to Trimethylethylene and Isobutylene (англ.) // Journal of the American Chemical Society. — 1933-10. — Vol. 55, iss. 10. — P. 4153–4157. — ISSN 0002-7863. — doi:10.1021/ja01337a042.
R. A. Benkeser, F. G. Belmonte. Reduction of alkynes by a new reducing system (англ.) // The Journal of Organic Chemistry. — 1984-05. — Vol. 49, iss. 9. — P. 1662–1664. — ISSN 0022-3263. — doi:10.1021/jo00183a038.
Michal Sklenár, Vladimír Danielik, Pavol Hudec. Discontinuous alkylation of diphenylamine with nonene for maximum catalyst utilization (англ.) // Chemical Papers. — 2017-08. — Vol. 71, iss. 8. — P. 1453–1461. — ISSN 2585-7290. — doi:10.1007/s11696-017-0139-2.
James D Burrington, John R Johnson, Paul A Lewis. Catalytic isomerization and dechlorination of nonenes (англ.) // Applied Catalysis A: General. — 2001-03. — Vol. 210, iss. 1-2. — P. 193–206. — doi:10.1016/S0926-860X(00)00825-5.
Sitan Wang, Xuan Meng, Yuan Zhong, Kande Liu, Naiwang Liu, Li Shi. A novel method for synthesis of nonylated diphenylamine by alkylation of diphenylamine with nonene over Fe-promoted SO42-/ZrO2 catalysts // Journal of Environmental Chemical Engineering. — 2024-08-01. — Т. 12, вып. 4. — С. 113047. — ISSN 2213-3437. — doi:10.1016/j.jece.2024.113047.
Цуй Айцзюнь, Чжэн Бинь, Хэ Минъян, Чэнь Цюнь. Реакция алкилирования нонена и дифениламина под действием катализатора на основе ионной жидкости (неопр.). d.wanfangdata.com.cn. doi:10.3969/j.issn.1003-9384.2010.02.017. Дата обращения: 6 марта 2026.
Fiege, H. Phenol Derivatives : [англ.] / H. Fiege, H. W. Voges, T. Hamamoto … [et al.]. — Wiley-VCH Verlag GmbH & Co. KGaA, 2000-06-15. — P. a19_313. — ISBN 978-3-527-30673-2. — doi:10.1002/14356007.a19_313. Архивная копия от 28 сентября 2022 на Wayback Machine

elsevier.com (Global: 365^th place; Russian: 501^st place)

linkinghub.elsevier.com

James D Burrington, John R Johnson, Paul A Lewis. Catalytic isomerization and dechlorination of nonenes (англ.) // Applied Catalysis A: General. — 2001-03. — Vol. 210, iss. 1-2. — P. 193–206. — doi:10.1016/S0926-860X(00)00825-5.

nih.gov (Global: 5^th place; Russian: 11^th place)

pubchem.ncbi.nlm.nih.gov

PubChem. 3-Nonene, (3E)- (англ.). pubchem.ncbi.nlm.nih.gov. Дата обращения: 6 марта 2026.

nist.gov (Global: 708^th place; Russian: 1,056^th place)

webbook.nist.gov

NIST Office of Data and Informatics. 2-Nonene (англ.). webbook.nist.gov. Дата обращения: 6 марта 2026.
NIST Office of Data and Informatics. 3-Nonene, (E)- (англ.). webbook.nist.gov. Дата обращения: 6 марта 2026.

nvlpubs.nist.gov

Thomas W. Mears, Abraham Fookson, Philip Pomerantz, Edwin H. Rich, Cecil S. Dussinger, and Frank L. Howard. Syn theses and Properties of Two Olefins, Six Paraffins, and Their Intermediates (англ.) // Journal of Research of the National Bureau of Standards. — 1950. — March (vol. 44). — P. 299-311.

sciencedirect.com (Global: 137^th place; Russian: 197^th place)

Sitan Wang, Xuan Meng, Yuan Zhong, Kande Liu, Naiwang Liu, Li Shi. A novel method for synthesis of nonylated diphenylamine by alkylation of diphenylamine with nonene over Fe-promoted SO42-/ZrO2 catalysts // Journal of Environmental Chemical Engineering. — 2024-08-01. — Т. 12, вып. 4. — С. 113047. — ISSN 2213-3437. — doi:10.1016/j.jece.2024.113047.

sigmaaldrich.com (Global: 774^th place; Russian: 4,907^th place)

trans-3-Nonene (англ.).

springer.com (Global: 182^nd place; Russian: 283^rd place)

materials.springer.com

Mass Density of Non-2-ene (pure) (англ.). SpringerMaterials. Дата обращения: 6 марта 2026.
Mass Density of trans-non-2-ene (pure) (англ.). SpringerMaterials. Дата обращения: 6 марта 2026.

link.springer.com

Michal Sklenár, Vladimír Danielik, Pavol Hudec. Discontinuous alkylation of diphenylamine with nonene for maximum catalyst utilization (англ.) // Chemical Papers. — 2017-08. — Vol. 71, iss. 8. — P. 1453–1461. — ISSN 2585-7290. — doi:10.1007/s11696-017-0139-2.

wanfangdata.com.cn (Global: 7,189^th place; Russian: low place)

d.wanfangdata.com.cn

Цуй Айцзюнь, Чжэн Бинь, Хэ Минъян, Чэнь Цюнь. Реакция алкилирования нонена и дифениламина под действием катализатора на основе ионной жидкости (неопр.). d.wanfangdata.com.cn. doi:10.3969/j.issn.1003-9384.2010.02.017. Дата обращения: 6 марта 2026.

web.archive.org (Global: 1^st place; Russian: 1^st place)

Fiege, H. Phenol Derivatives : [англ.] / H. Fiege, H. W. Voges, T. Hamamoto … [et al.]. — Wiley-VCH Verlag GmbH & Co. KGaA, 2000-06-15. — P. a19_313. — ISBN 978-3-527-30673-2. — doi:10.1002/14356007.a19_313. Архивная копия от 28 сентября 2022 на Wayback Machine

wiley.com (Global: 150^th place; Russian: 194^th place)

onlinelibrary.wiley.com

Johan A. Martens, Wim H. Verrelst, Georges M. Mathys, Stephen H. Brown, Pierre A. Jacobs. Tailored Catalytic Propene Trimerization over Acidic Zeolites with Tubular Pores (англ.) // Angewandte Chemie International Edition. — 2005-09-05. — Vol. 44, iss. 35. — P. 5687–5690. — ISSN 1433-7851. — doi:10.1002/anie.200463045.
Fiege, H. Phenol Derivatives : [англ.] / H. Fiege, H. W. Voges, T. Hamamoto … [et al.]. — Wiley-VCH Verlag GmbH & Co. KGaA, 2000-06-15. — P. a19_313. — ISBN 978-3-527-30673-2. — doi:10.1002/14356007.a19_313. Архивная копия от 28 сентября 2022 на Wayback Machine

worldcat.org (Global: 4^th place; Russian: 3^rd place)

Johan A. Martens, Wim H. Verrelst, Georges M. Mathys, Stephen H. Brown, Pierre A. Jacobs. Tailored Catalytic Propene Trimerization over Acidic Zeolites with Tubular Pores (англ.) // Angewandte Chemie International Edition. — 2005-09-05. — Vol. 44, iss. 35. — P. 5687–5690. — ISSN 1433-7851. — doi:10.1002/anie.200463045.
Frank C. Whitmore, L. W. Mixon. Polymerization of Olefins. IV. 1 The Nonenes from the Dehydration and Copolymerization of t-Butyl and t-Amyl Alcohols 2 (англ.) // Journal of the American Chemical Society. — 1941-05. — Vol. 63, iss. 5. — P. 1460–1462. — ISSN 0002-7863. — doi:10.1021/ja01850a092.
George C. Johnson, Frank S. Fawcett. Inter-polymerization of Isobutene and 2-Methyl-2-butene Using an Alumina-Silica Catalyst. Composition of the Hydrogenated Nonenes (англ.) // Journal of the American Chemical Society. — 1946-08. — Vol. 68, iss. 8. — P. 1416–1419. — ISSN 0002-7863. — doi:10.1021/ja01212a005.
Frank C. Whitmore, E. E. Stahly. The Common Basis of Intramolecular Rearrangements. II. 1 The Dehydration of Di-tert-butylcarbinol and the Conversion of the Resulting Nonenes to Trimethylethylene and Isobutylene (англ.) // Journal of the American Chemical Society. — 1933-10. — Vol. 55, iss. 10. — P. 4153–4157. — ISSN 0002-7863. — doi:10.1021/ja01337a042.
R. A. Benkeser, F. G. Belmonte. Reduction of alkynes by a new reducing system (англ.) // The Journal of Organic Chemistry. — 1984-05. — Vol. 49, iss. 9. — P. 1662–1664. — ISSN 0022-3263. — doi:10.1021/jo00183a038.
Michal Sklenár, Vladimír Danielik, Pavol Hudec. Discontinuous alkylation of diphenylamine with nonene for maximum catalyst utilization (англ.) // Chemical Papers. — 2017-08. — Vol. 71, iss. 8. — P. 1453–1461. — ISSN 2585-7290. — doi:10.1007/s11696-017-0139-2.
Sitan Wang, Xuan Meng, Yuan Zhong, Kande Liu, Naiwang Liu, Li Shi. A novel method for synthesis of nonylated diphenylamine by alkylation of diphenylamine with nonene over Fe-promoted SO42-/ZrO2 catalysts // Journal of Environmental Chemical Engineering. — 2024-08-01. — Т. 12, вып. 4. — С. 113047. — ISSN 2213-3437. — doi:10.1016/j.jece.2024.113047.

Нонены (Russian Wikipedia)

acs.org (Global: 865th place; Russian: 1,368th place)

pubs.acs.org

chemicalbook.com (Global: 9,407th place; Russian: low place)

dguv.de (Global: 690th place; Russian: 7,541st place)

gestis.dguv.de

doi.org (Global: 2nd place; Russian: 5th place)

dx.doi.org

elsevier.com (Global: 365th place; Russian: 501st place)