This article is cited in 3 scientific papers (total in 3 papers)
Highly diastereocelective one-pot four-component coupling of p-TolSCI, 1-methoxycycloalkene, methyl vinyl ether and a carbon nucleophile leading to the synthesis of polyfunctional compounds
Abstract:
An one-pot TiCl4 initiated assemblage of polyfunctional compounds via a sequential coupling of p-TolSCl, 1-methoxycycloalkene, methyl vinyl ether and Sn- or Si-capped carbon nucleophile is shown to proceed with high diastereoselectivity at all newly created chiral centres.
Document Type:
Article
Language: English
Citation:
M. I. Lazareva, Yu. K. Kryschenko, R. Caple, V. G. YoungJr, W. A. Smit, “Highly diastereocelective one-pot four-component coupling of p-TolSCI, 1-methoxycycloalkene, methyl vinyl ether and a carbon nucleophile leading to the synthesis of polyfunctional compounds”, Mendeleev Commun., 9:1 (1999), 24–25
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https://www.mathnet.ru/eng/mendc4510
https://www.mathnet.ru/eng/mendc/v9/i1/p24
This publication is cited in the following 3 articles:
M. I. Lazareva, S. T. Nguyen, M. Ch. Nguyen, H. Emiru, N. A. McGrath, R. Caple, W. A. Smit, “μ-Alkyne dicobalt hexacarbonyl complexes of conjugated enynes as substrates in the arylthio-mediated stepwise AdE reactions”, Mendeleev Commun., 11:6 (2001), 224–227
Margarita I. Lazareva, Yury K. Kryschenko, Ron Caple, Victor G. Young Jr., William A. Smit, “ChemInform Abstract: Highly Diastereoselective One‐Pot Four‐Component Coupling of p‐TolSCl, 1‐Methoxycycloalkene, Methyl Vinyl Ether, and a Carbon Nucleophile Leading to the Synthesis of Polyfunctional Compounds.”, ChemInform, 30:30 (1999)
M. I. Lazareva, Yu. K. Kryschenko, R. Caple, W. A. Smit, K. A. Lyssenko, A. S. Shashkov, “Diastereoselective synthesis of polyfunctional compounds based on the tandem sequence of threeAd E reactions using cyclic vinyl ethers as first alkene components”, Russ Chem Bull, 49:1 (1990), 85
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