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2007 Organo-selenium compounds S 0130 Multicomponent Reactions of Allenes, Diaryl Diselenides, and Nucleophiles in the Presence of Iodosobenzene Diacetate: Direct Synthesis of 3-Functionalized-2-aryl- selenyl Substituted Allyl Derivatives. — Multicomponent reaction of aryl substituted allenes, diphenyl diselenide and oxygen nucleophiles offers a facile synthesis of vari- ous title compounds. When alkyl-substituted allenes (V) are used, the attack of the oxygen nucleophile occurs at the C-3 carbon. — (YU, L.; CHEN, B.; HUANG*, X.; Tetrahedron Lett. 48 (2007) 6, 925-927; Dep. Chem., Zhejiang Univ., Hangzhou 310028, Peop. Rep. China; Eng.) — Mais 20- 171

Multicomponent Reactions of Allenes, Diaryl Diselenides, and Nucleophiles in the Presence of Iodosobenzene Diacetate: Direct Synthesis of 3-Functionalized-2-arylselenyl Substituted

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Page 1: Multicomponent Reactions of Allenes, Diaryl Diselenides, and Nucleophiles in the Presence of Iodosobenzene Diacetate: Direct Synthesis of 3-Functionalized-2-arylselenyl Substituted

2007

Organo-selenium compoundsS 0130 Multicomponent Reactions of Allenes, Diaryl Diselenides, and Nucleophiles in the

Presence of Iodosobenzene Diacetate: Direct Synthesis of 3-Functionalized-2-aryl-selenyl Substituted Allyl Derivatives. — Multicomponent reaction of aryl substituted allenes, diphenyl diselenide and oxygen nucleophiles offers a facile synthesis of vari-ous title compounds. When alkyl-substituted allenes (V) are used, the attack of the oxygen nucleophile occurs at the C-3 carbon. — (YU, L.; CHEN, B.; HUANG*, X.; Tetrahedron Lett. 48 (2007) 6, 925-927; Dep. Chem., Zhejiang Univ., Hangzhou 310028, Peop. Rep. China; Eng.) — Mais

20- 171