Synthetic studies towards mniopetals (I). A short synthesis of a key intermediate for the total synthesis of mniopetals

Synlett

Volumn , Issue 8, 1999, Pages 1325-1327

  Jauch, Johann ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

Diastereoselective Baylis Hillman reaction; HIV; Intramolecular Diels Alder reaction; Natural products; Terpenoids

Indexed keywords

ANTIVIRUS AGENT; MNIOPETAL; NATURAL PRODUCT; SESQUITERPENE DERIVATIVE; TERPENOID; UNCLASSIFIED DRUG;

ANTIVIRAL ACTIVITY; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; DIASTEREOISOMER; HUMAN IMMUNODEFICIENCY VIRUS 1; OXIDATION; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0032790303     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2796     Document Type: Article

References (23)

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20. 3): 170.6; 143.3; 142.9; 139.8; 135.5; 133.6; 130.3; 130.2; 129.6; 127.6; 126.3; 99.1; 79.1; 67.1; 64.2; 47.7; 40.3; 38.1; 35.7; 34.1; 31.4; 30.5; 27.2; 27.0; 26.8; 25.3; 23.1; 22.2; 20.8; 19.2; 15.8.
21. 11 (figure presented)
22. 3): 175.7; 135.6; 135.5; 133.4; 133.3; 131.6; 129.9; 128.6; 127.8; 97.7; 77.8; 76.0; 63.4; 58.4; 52.0; 48.6; 47.6; 39.8; 38.9; 38.8; 34.2; 34.1; 32.0; 31.3; 27.0; 26.6; 25.0; 22.6; 22.2; 21.7; 21.1; 19.3; 15.1.
23. Together with 14 we found small quantities of two other products which have not yet been structurally fully characterized.