Gem-dimethyl effect in the formation of seven to eleven-membered ring lactones by iodolactonisation

Tetrahedron Letters

Volumn 34, Issue 28, 1993, Pages 4527-4530

  Simonot, Bruno ^a   Rousseau, Gérard ^a  

^a UNIVERSITÉ PARIS SUD   (France)

Author keywords

[No Author keywords available]

Indexed keywords

LACTONE DERIVATIVE; MACROCYCLIC COMPOUND;

ARTICLE; CYCLIZATION; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0027223995     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(93)88076-U     Document Type: Article

References (24)

1. Addition Reactions with Intramolecular Cyclisation
2. The Effect of Geminal Substitution Ring Size and Rotamer Distribution on the Intramolecular Nucleophilic Catalysis of the Hydrolysis of Monophenyl Esters of Dibasic Acids and the Solvolysis of the Intermediate Anhydrides
3. The Synthesis of Bis(gem-dimethyl)cycloalkanones and Tetrakis(gem-dimethyl)cycloalkanediones.
4. gem-Dimethyl-substituted Cyclic Anhydrides.
5. Ring-closure reactions. 12. gem-dimethyl effect in some medium and large rings
6. Silicon-mediated annulation. Part 2. A synthesis of ?-alkoxy cyclo-octanones via intramolecular directed aldol reactions