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  • Development of the intramolecular Prins cyclization/Schmidt reaction for the construction of the azaspiro[4,4]nonane: application to the formal synthesis of (±)-stemonamine.

Development of the intramolecular Prins cyclization/Schmidt reaction for the construction of the azaspiro[4,4]nonane: application to the formal synthesis of (±)-stemonamine.

Organic letters (2011-01-15)
Zhi-Hua Chen, Yong-Qiang Tu, Shu-Yu Zhang, Fu-Min Zhang
ABSTRACT

A TiCl(4)-promoted tandem intramolecular Prins cyclization/Schmidt reaction has been designed and developed to be an efficient method for the construction of the azaspiro[4,4]nonane. The present tandem protocol has been employed to construct the tricyclic azaquaternary skeleton (ring A, B, and C) of stemonamine.

MATERIALS
Product Number
Brand
Product Description

Supelco
Nonane, analytical standard
Sigma-Aldrich
Nonane, anhydrous, ≥99%
Sigma-Aldrich
Nonane, ReagentPlus®, 99%