The first route toward oxygenated monocarbocyclic terpenoids: Synthesis of elegansidiol, a new sesquiterpene from Santolina elegans

Tetrahedron Letters

Volumn 40, Issue 47, 1999, Pages 8273-8276

  Barrero, Alejandro F ^a   Alvarez Manzaneda, Enrique J ^a   Herrador, M Mar ^a   Alvarez Manzaneda, R ^b   Quilez, J ^a   Chahboun, R ^a   Linares, P ^a   Rivas, A ^a  

^a UNIVERSITY OF GRANADA   (Spain)

^b UNIVERSITY OF ALMERÍA   (Spain)

Author keywords

Cyclization; Terpenoids

Indexed keywords

CYCLOHEXANOL DERIVATIVE; GERANYL ACETATE; NATURAL PRODUCT; SESQUITERPENE; TERPENOID; TRITERPENE;

ARTICLE; CYCLIZATION; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; MEDICINAL PLANT; NONHUMAN; STRUCTURE ANALYSIS;

SANTOLINA;

EID: 0033584836     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01730-X     Document Type: Article

References (6)

1. Barrero, A. F.; Manzaneda, E. A.; Manzaneda, R. A. Tetrahedron Lett. 1989, 30, 3351-3352.
2. Van Tamelen, E. E.; Estornia, A.; Hessler, E. J.; Schwartz, M. J. Am. Chem. Soc. 1963, 85, 3295-3296.
3. Amico, V. Phytochemistry 1995, 39, 1257-1279.
4. Barrero, A. F.; Manzaneda, E. A.; Linares, P. P. Tetrahedron 1994, 50, 13239-13250.
5. Armstrong, R. J.; Weiler, L. Can. J. Chem. 1986, 64, 584-596.
6. 3CSi), 27.0 (C-1), 32.0 (C-3′), 40.4 (C-6′), 43.2 (C-3), 52.3 (C-1′), 76.8 (C-5′), 109.1 (C-7′), 148.1 (C-2′), 209.7 (C-2).