1,1,3,3-tetramethyl-2-methyleneindan derivatives: syntheses with imminent rearrangement
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. Sterically congested molecules. Part 4. Front strain along a C–C double bond in the crystal structure of [1-(1,1,3,3-tetramethylindan-2-ylidene)-1-(trimethylsilyl)methyl] 2-trimethylsilylphenyl thioether
2. Front strain in the structure of 2-benzylidene-1,1,3,3-tetramethylindan, a sterically congested styrene
3. Sterically congested molecules. 5. Trimeric [.alpha.-(1,1,3,3-tetramethyl-2-indanylidene)benzyl]lithium: structural example of an unsolvated vinyllithium derivative
4. Substituent-induced chemical shifts along CC double bonds
5. ( E,Z ) Equilibria, 14. Substituent‐Induced Chemical Shifts along the C = N Bond of Schiff Bases
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