Catalytic enantioselective diels-alder addition to furan provides a direct synthetic route to many chiral natural products

Tetrahedron Letters

Volumn 34, Issue 25, 1993, Pages 3979-3982

  Corey, E J ^a   Loh, Teck Peng ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

7 OXABICYCLO[2.2.1]HEPTANE DERIVATIVE; FURAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ENANTIOMER; METHODOLOGY; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0027160174     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)60594-4     Document Type: Article

References (20)

1. Optically Pure 7-Oxabicyclo[2.2.1]hept-5-en-2-yl Derivatives ("Naked Sugars") as New Chirons
2. Synthesis of 9,11-epoxy-9a-homoprostaglandin analogues
3. High-pressure Diels-Alder Reactions of Furans with a-Chiloro- and a-Acetoxyacrylonitrile
4. Highly Stereoselective Synthesis of (±)-Aminobromocyclitol Derivatives from Furan
5. Cycloadditions of 3-methoxyfuran with mono-activated dienophiles; application to the synthesis of (�)-avenaciolides
6. Total synthesis of (+)-(1,2,3/4,5)-2,3,4,5-tetrahydroxycyclohexane-1-methanol and (+)-(1,3/2,4,5)-5-amino-2,3,4-trihydroxycyclohexane-1-methanol [(+)-validamine]. X-Ray crystal structure of (3S)-(+)-2-exo-bromo-4,8-dioxatricyclo[4.2.1.O]nonan-5-one
7. Syntheses of (+)- and (-)-Methyl 8-Epinonactate and (+)- and (-)-Methyl Nonactate