Synthesis, structure and reactivity of a macrocyclic imine: aza-[13]-macrodiolides
Author:
Funder
NSF
NSF-REU
NSF-CRIF
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference46 articles.
1. A diversity-oriented synthesis approach to macrocycles via oxidative ring expansion
2. Diastereoselectivity in Epoxidation of Carbohydrate Fused [13]-Macro-dilactones
3. Remote induction of asymmetry in [13]-macro-dilactone topology by a single stereogenic center
4. Positioning and Configuration of Key Atoms Influence the Topology of [13]-Macrodiolides
5. Stereochemical Control of Skeletal Diversity
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