• Bulletin of the Korean Chemical Society
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• v.29 no.4
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• pp.876-878
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• 2008

• Bulletin of the Korean Chemical Society
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• v.25 no.9
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• pp.1351-1354
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• 2004

Tetracyclic 5-azaindole analogues were prepared by palladium-catalyzed sequential annulation of benzylidene(3-iodopyridinyl-4-yl)amine and 1-aryl substituted internal alkynes under $Pd(OAc)_2,\;n-Bu_4NCl,\;and Et_3N\;at\;120^{\circ}C.$ The synthetic procedure showed possible diversification of tetracyclic 5-azaindole analogues by varying the 1-aryl substituent in internal alkynes.

• Bulletin of the Korean Chemical Society
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• v.29 no.9
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• pp.1815-1818
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• 2008

• Bulletin of the Korean Chemical Society
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• v.8 no.4
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• pp.310-313
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• 1987

A dianion-mediated dialkylation reaction provides a variety of propellanes. 12-Thia[4.4.3] propel-3-ene, 3-(N-benzyl)-2,4-dioxotricyclo[3.3.3.0] decane and 3-(N-benzyl)-2,4-dioxotricyclo[3.3.3.0] nonane were prepared by this dianion ring annulation methodology.

• Journal of the Korean Chemical Society
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• v.38 no.1
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• pp.80-86
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• 1994

The synthetic pathway of ethyl $({\pm})$-8-oxo-10-oxa-l'H-spiro[1, 3]dioxolane-4,4'-tricyclo [9.2.1.0 1,6]dodec-6-ene-9-carboxylate (7), an important intermediate for the total synthesis of bruceantin analogue, was developed. Ethyl 2-cyclohexanonecarboxylate and methyl vinyl ketone were employed as starting materials. Robinson annulation, allylic oxidation, regiospecific acylation and the formation of epoxy methano bridge ring were studied. 4,4a,5,6,7,8-Hexahydro-4a-hydroxy-2(3H)naphthalenone (14) was synthesized utilizing the unusual decarboethoxylation reaction discovered during ketalization of octalone (3).

• Bulletin of the Korean Chemical Society
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• v.25 no.4
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• pp.441-442
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• 2004