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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 37, 2007 - Issue 12
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Original Articles

Simple, One‐Pot Procedure for the Generation of Homoallylic Alcohols from Barbier‐Type Allylation of Gem‐diacetates in the Presence of β‐Cyclodextrin in Water

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Pages 1983-1988 | Received 26 Oct 2006, Published online: 22 Jun 2007

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NitinA. Mirgane & AnilV. Karnik. (2011) Aqueous ethanol: a suitable medium for the diastereoselective Diels–Alder reaction mediated by chiral bases. Green Chemistry Letters and Reviews 4:3, pages 269-272.
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Articles from other publishers (5)

Rodney A. Fernandes, Gujjula V. Ramakrishna & Venkati Bethi. (2020) MnO 2 as a terminal oxidant in Wacker oxidation of homoallyl alcohols and terminal olefins . Organic & Biomolecular Chemistry 18:31, pages 6115-6125.
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Joaquin García‐Álvarez, Eva Hevia & Vito Capriati. (2015) Reactivity of Polar Organometallic Compounds in Unconventional Reaction Media: Challenges and Opportunities. European Journal of Organic Chemistry 2015:31, pages 6779-6799.
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Chao Han, Wei Meng, Hao Liu, Yanping Liu & Jingchao Tao. (2014) DMAP-catalyzed four-component one-pot synthesis of highly functionalized spirooxindole-1,4-dihydropyridines derivatives in aqueous ethanol. Tetrahedron 70:45, pages 8768-8774.
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Fumiaki Ono, Kuniaki Nishioka, Shirou Itami, Hirotaka Takenaka & Tsuneo Sato. (2008) An Improved Method for the Synthesis of Allylic gem -Diacetates from α,β-Unsaturated Aldehydes Catalyzed by Lithium Tetrafluoroborate . Chemistry Letters 37:12, pages 1248-1249.
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M. Somi Reddy, M. Narender, Y. V. D. Nageswar & K. Rama Rao. (2007) Simple, One‐Pot Procedure for the Generation of Homoallylic Alcohols from Barbier‐Type Allylation of Gem‐Diacetates in the Presence of β‐Cyclodextrin in Water.. ChemInform 38:45.
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