Title : Cyclopentannulation of 3-alkylindoles: a synthesis of a tetracyclic subunit of the kopsane alkaloids.

Pub. Date : 2001 Jun 29

PMID : 11421796






3 Functional Relationships(s)
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1 Indoles which bear an alkyl substituent in the 3-position undergo a [3 + 2] annulation reaction when treated with 1,1-cyclopropane diesters in the presence of Yb(OTf)(3) resulting in 2,3-cyclopentanoindolines. Indoles POU class 5 homeobox 1 Homo sapiens
2 Indoles which bear an alkyl substituent in the 3-position undergo a [3 + 2] annulation reaction when treated with 1,1-cyclopropane diesters in the presence of Yb(OTf)(3) resulting in 2,3-cyclopentanoindolines. 1,1-cyclopropane diesters POU class 5 homeobox 1 Homo sapiens
3 Indoles which bear an alkyl substituent in the 3-position undergo a [3 + 2] annulation reaction when treated with 1,1-cyclopropane diesters in the presence of Yb(OTf)(3) resulting in 2,3-cyclopentanoindolines. 2,3-cyclopentanoindolines POU class 5 homeobox 1 Homo sapiens