Stereocontrolled intramolecular cyclization of ω-tributylstannyl ether aldehydes. synthesis of the 6·7·7·6 ring system of polycyclic ethers
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Recent progress in synthetic chemistry of cyclic ether derivatives.
2. Stereocontrolled Second Generation Syntheses of the ABC and FG Ring Systems of Brevetoxin B
3. A new approach to the construction of .beta.-alkoxy-substituted cyclic ethers via the intramolecular cyclization of .omega.-trialkylplumbyl and .omega.-trialkylstannyl ether acetals
4. Synthetic studies on the dioxepane region of brevetoxin B. New synthetic technology for the construction of oxepanes and synthesis of a model for the CDEF ring skeleton of brevetoxin B
5. Bridging of macrodithionolactones to bicyclic systems. Synthesis and modeling of oxapolycyclic frameworks
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