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Publication Type : Journal Article
Thematic Areas : Biotech
Publisher : Elsevier
Source : Tetrahedron letters, Elsevier, Volume 35, Number 37, p.6907–6908 (1994)
Url : http://www.sciencedirect.com/science/article/pii/0040403994850380
Campus : Amritapuri
School : School of Biotechnology
Center : Biotechnology, Phytochemistry Labs, Sanitation Biotechnology
Department : biotechnology, Chemistry
Year : 1994
Abstract : The total synthesis of epijasmonoids, (±)-methyl cucurbate and (±)-methyl epijasmonate is described starting from aldehyde 14, where the key step is a highly stereocontrolled 5- (3,4) ene cyclization 17 → 18.
Cite this Research Publication : T. K. Sarkar, Ghorai, B. K., and Banerji, A., “Intramolecular alder ene approach to stereochemical control over three contiguous stereogenic centres: Synthesis of (+-)-methyl cucurbate and (+-)-methyl epijasmonate”, Tetrahedron letters, vol. 35, pp. 6907–6908, 1994.