Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 23, 1993 - Issue 5
Submit an article Journal homepage
48
Views
21
CrossRef citations to date
0
Altmetric
Original Articles

A Novel Route to Substituted Trienes and Tetraenes

Tomasz Janecki Institute of Organic Chemistry, Technical University, Zwirki 36, 90-924, Łódz, Poland
Pages 641-650 | Received 14 Sep 1992, Published online: 27 Oct 2006

Citations (21)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

De Qing Shi & Ru Yu Chen. (2000) A STEREOSELECTIVE SYNTHESIS OF UNSATURATED PHOSPHONATES BY WITTIG-HORNER REACTIONS OF BISPHOSPHONYLMETHANE WITH 5-ARYL-(3-METHYL)-2E,4E-PENTADIENALS. Phosphorus, Sulfur, and Silicon and the Related Elements 164:1, pages 229-237.
Read now
FanieR. van Heerden, JohanJ. Huyser & CedricW. Holzapfel. (1994) Preparation of Multifunctional Stereodefined Dienes. Synthetic Communications 24:20, pages 2863-2872.
Read now

Articles from other publishers (19)

Prashant Shukla, Ambika Asati, Devkumari Patel, Manorama Singh, Vijai K. Rai & Ankita Rai. (2023) Novel Synergistic Catalysis by Ethylcarbodiimide Hydrochloride Salt and CuI Towards Morita‐Baylis‐Hillman Reaction. ChemistrySelect 8:5.
Crossref
Maria Kalyva, Alexandros L. ZografosEra Kapourani, Evaggelos Giambazolias, Laurent DevelAthanasios PapakyriakouVincent DiveYannis G. LazarouDimitris Georgiadis. (2015) Probing the Mechanism of Allylic Substitution of Morita–Baylis–Hillman Acetates (MBHAs) by using the Silyl Phosphonite Paradigm: Scope and Applications of a Versatile Transformation. Chemistry – A European Journal 21:8, pages 3278-3289.
Crossref
Cheol Hee Lim, Sung Hwan Kim, Ko Hoon Kim & Jae Nyoung Kim. (2013) An efficient synthesis of o-terphenyls from Morita–Baylis–Hillman adducts of cinnamaldehydes: a consecutive bromination, Wittig reaction, 6π-electrocyclization, and an aerobic oxidation process. Tetrahedron Letters 54:20, pages 2476-2479.
Crossref
Min Shi, Feijun Wang, Mei-Xin Zhao & Yin WeiMei-Xin Zhao, Yin Wei & Min Shi. 2011. The Chemistry of the Morita-Baylis-Hillman Reaction. The Chemistry of the Morita-Baylis-Hillman Reaction 209 324 .
Ewa Krawczyk & Krzysztof Owsianik. (2011) An unusual regiochemistry of reactions of a cyclohexenylphosphonate bearing a β-ethoxycarbonyl group with aldehydes. Tetrahedron 67:10, pages 1938-1947.
Crossref
Larry E. Overman & Mark D. Rosen. (2010) Terminating catalytic asymmetric Heck cyclizations by stereoselective intramolecular capture of η3-allylpalladium intermediates: total synthesis of (−)-spirotryprostatin B and three stereoisomers. Tetrahedron 66:33, pages 6514-6525.
Crossref
Goverdhan Mehta & H. Surya Prakash Rao. 2009. PATAI'S Chemistry of Functional Groups. PATAI'S Chemistry of Functional Groups.
Ewa Krawczyk, Krzysztof Owsianik & Aleksandra Skowrońska. (2005) Regio- and stereoselective reactions between cyclic Baylis–Hillman type adducts and N-nucleophiles and P-nucleophile. Tetrahedron 61:6, pages 1449-1457.
Crossref
Philippe Savignac & Bogdan Iorga. 2003. Modern Phosphonate Chemistry. Modern Phosphonate Chemistry.
Deevi Basavaiah, Anumolu Jaganmohan Rao & Tummanapalli Satyanarayana. (2003) Recent Advances in the Baylis−Hillman Reaction and Applications. Chemical Reviews 103:3, pages 811-892.
Crossref
Ewa Krawczyk, Krzysztof Owsianik, Aleksandra Skowrońska, Michał Wieczorek & Wiesław Majzner. (2002) An expedient, stereoselective synthesis of highly functionalized cyclic compounds. New J. Chem. 26:12, pages 1753-1767.
Crossref
João N Rosa, Carlos A.M Afonso & António G Santos. (2001) Ionic liquids as a recyclable reaction medium for the Baylis–Hillman reaction. Tetrahedron 57:19, pages 4189-4193.
Crossref
Larry E. Overman & Mark D. Rosen. (2000) Total Synthesis of (−)-Spirotryprostatin B and Three Stereoisomers. Angewandte Chemie International Edition 39:24, pages 4596-4599.
Crossref
Larry E. Overman & Mark D. Rosen. (2000) Totalsynthese von (−)-Spirotryprostatin B und drei Stereoisomeren. Angewandte Chemie 112:24, pages 4768-4771.
Crossref
Engelbert Ciganek. 2004. Organic Reactions. Organic Reactions 201 350 .
Deevi Basavaiah, Polisetti Dharma Rao & Rachakonda Suguna Hyma. (1996) The Baylis-Hillman reaction: A novel carbon-carbon bond forming reaction. Tetrahedron 52:24, pages 8001-8062.
Crossref
Tohru Oishi, Hiroki Oguri & Masahiro Hirama. (1995) Asymmetric Baylis-Hillman reactions using chiral 2,3-disubstituted 1,4-diazabicyclo[2.2.2]octanes catalysts under high pressure conditions. Tetrahedron: Asymmetry 6:6, pages 1241-1244.
Crossref
E.Peter Kündig, He Xu Long, Patrick Romanens & Gérald Bernardinelli. (1993) Highly diastereoselective coupling reactions between chiral benzaldehyde tricarbonylchromium complexes and activated double bonds. Tetrahedron Letters 34:44, pages 7049-7052.
Crossref
T. JANECKI. (2010) ChemInform Abstract: A Novel Route to Substituted Trienes and Tetraenes.. ChemInform 24:26, pages no-no.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.