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Syntheses and Reactions of Allyl Phenylselenides. A Convenient Method of the Allyl Methylcarbamates Synthesis

Ścianowski J., Tafelska-Kaczmarek A.

Polish Journal of Chemistry

2007

Vol. 81, nr 4

529-534

Allyl phenylselenides from terpene systems are convenient precursors for the synthesis of the terpene allyl alcohols and allyl methylcarbamates. Using optically active allyl phenylselenides corresponding optically active oxygen and nitrogen derivatives were obtained. A new one-step method of the allyl methylcarbamates synthesis from allyl phenylselenides was described.

Synthesis and Reactions of Organic Compounds with a Nitrogen Atom. Part XVII. Reactions of Acyclic and Monocyclic Chlorides with Phenylselenosodium

Bąkowska-Janiszewska J., Ścianowski J., Uzarewicz A.

Polish Journal of Chemistry

2001

Vol. 75, nr 5

649-656

The reaction of neryl (3), geranyl (4), (+)-carvotanacetyl (5), (-)-carvyl (6) and perillyl (7) chlorides with phenylseleno- (1) or phenyltellurosodium (2), and then with chloramine- T afforded _,_-unsaturated toluenesulfonamides 8-11, which were reduced with sodium in liquid ammonia to allylic amines 12-15. Allylic phenyltellurides were oxidized by air to carbonyl compounds 29-31 or alcohol 28.

Synthesis and Reactions of Organic Compounds with a Nitrogen Atom : Part XVI. Reactions of (-)-4Chloro-3(10)-carene and (+)-10-Chloro-3-carene with Phenyltelluro- and Phenylselenosodium

Uzarewicz A., Ścianowski J., Bąkowska-Janiszewska J.

Polish Journal of Chemistry

2000

Vol. 74, nr 8

1079-1083

Synthesis and Reactions of Organic Compounds with a Nitrogen Atom : Part XV : Reactions of (+)-3-Chloro-2(10)-pinene and (-)-10-Chloro-2-pinene with Phenyltelluro- and Phenylselenosodium

Uzarewicz A., Ścianowski J., Bąkowska-Janiszewska J.

Polish Journal of Chemistry

1999

Vol. 73, nr 11

1791-1796