Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 17, 1987 - Issue 7
49
Views
16
CrossRef citations to date
0
Altmetric
Original Articles

Asymmetric Synthesis of 2-Substituted Acrylate Esters

, , &
Pages 795-802 | Published online: 05 Dec 2006

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

Read on this site (1)

H. Amri, M.M. El Gaied & J. Villiéras. (1990) Hydroxyalkylation of Diethylvinylphosphonate in the Presence of DABCO. Synthetic Communications 20:5, pages 659-663.
Read now

Articles from other publishers (15)

Mateo M. Salgado, Alejandro Manchado, Carlos T. Nieto, David Díez & Narciso M. Garrido. (2021) Synthesis and Modeling of Ezetimibe Analogues. Molecules 26:11, pages 3107.
Crossref
Kui Yuan, Hong-Liang Song, Yinjun Hu & Xin-Yan Wu. (2009) Chiral phosphinothiourea-catalyzed asymmetric Morita–Baylis–Hillman reactions of acrylates with aromatic aldehydes. Tetrahedron 65:39, pages 8185-8190.
Crossref
Mayuko Suzuki, Yoshito Kawamoto, Takeo Sakai, Yasutomo Yamamoto & Kiyoshi Tomioka. (2008) Asymmetric Construction of Quaternary Carbon Centers by Sequential Conjugate Addition of Lithium Amide and in Situ Alkylation: Utility in the Synthesis of (−)-Aspidospermidine. Organic Letters 11:3, pages 653-655.
Crossref
. 2005. Synthesis of Naturally Occurring Nitrogen Heterocycles from Carbohydrates. Synthesis of Naturally Occurring Nitrogen Heterocycles from Carbohydrates 239 271 .
Varinder K. AggarwalDavid K. DeanAndrea MereuRichard Williams. (2001) Rate Acceleration of the Baylis−Hillman Reaction in Polar Solvents (Water and Formamide). Dominant Role of Hydrogen Bonding, Not Hydrophobic Effects, Is Implicated. The Journal of Organic Chemistry 67:2, pages 510-514.
Crossref
Engelbert Ciganek. 2004. Organic Reactions. Organic Reactions 201 350 .
George W. Kabalka & Richard M. Pagni. (1997) Organic reactions on alumina. Tetrahedron 53:24, pages 7999-8065.
Crossref
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
K. Smith, C. V. Fry & M. Tzimas. 1995. Chemistry of Waste Minimization. Chemistry of Waste Minimization 86 115 .
Siegfried E. Drewes, Neville D. Emslie, John S. Field, Abdullah A. Khan & Niyum S. Ramesar. (1993) A novel tetrahydrofuran derivative via a tertiary ketol-type rearrangement. Tetrahedron Letters 34:7, pages 1205-1208.
Crossref
Shu-Zhong Wang, Keiji Yamamoto, Harou Yamada & Takashi Takahashi. (1992) Stereochemical study on the palladium(O)-catalyzed carbonylation of 3-(methoxycarbonyloxy)-2-methylenealkanoates and analogues. Tetrahedron 48:12, pages 2333-2348.
Crossref
Siegfried E. Drewes, Neville D. Emslie, John S. Field, Abdullah A. Khan & Niyum Ramesar. (1992) Synthesis, resolution and assignment of absolute configuration of 2-(?-hydroxy)aryl acrylate esters. Tetrahedron: Asymmetry 3:2, pages 255-260.
Crossref
M. BRAND, S. E. DREWES, G. LOIZOU & G. H. P. ROOS. (2016) ChemInform Abstract: Asymmetric Synthesis of 2‐Substituted Acrylate Esters.. ChemInform 19:4.
Crossref
Siegfried E. Drewes & Gregory H.P. Roos. (1988) Synthetic potential of the tertiary-amine-catalysed reaction of activated vinyl carbanions with aldehydes. Tetrahedron 44:15, pages 4653-4670.
Crossref
. 1988. Annual Reports in Organic Synthesis–1987. Annual Reports in Organic Synthesis–1987 1 233 .

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:

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:

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.