Enantioselective total synthesis and assignment of the absolute configuration of (+)-laurokamurene B

Tetrahedron Asymmetry

Volumn 19, Issue 5, 2008, Pages 624-627

  Srikrishna, Adusumilli ^a   Beeraiah, Baire ^a   Ramesh Babu, R ^a  

^a INDIAN INSTITUTE OF SCIENCE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; CAMPHOLENALDEHYDE; LAUROKAMURENE B; SESQUITERPENE; UNCLASSIFIED DRUG;

ALGA; ARTICLE; CHEMICAL STRUCTURE; LAURENCIA OKAMURAI; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 40849112775     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.02.010     Document Type: Article

References (8)

1. Martin, J. D.; Darias, J. In Marine Natural Products.
2. Scheuer, P. J., Ed.; Academic Press: New York, 1978; Vol. I, pp 151-161.
3. Mao S.-C., and Guo Y.-W. J. Nat. Prod. 69 (2006) 1209-1211
4. Mao S.-C., and Guo Y.-W. Chin. Tradit. Herb. Drugs 35 (2004) 8-17
5. Srikrishna A., Khan I.A., Babu R.R., and Sajjanshetty A. Tetrahedron 63 (2007) 12616-12620
6. Liu H.-J., and Chan W.H. Can. J. Chem. 60 (1982) 1081-1091
7. 2 = 0.2595, GOF = 1.029, restrained GOF = 1.029 for all data. An ORTEP diagram of 12 is depicted below. Crystallographic data has been deposited with Cambridge Crystallographic Data Centre (CCDC 675955).{A figure is presented}
8. 2S: C, 61.19; H, 7.53; N, 9.51; S, 10.89. Found: C, 60.91; H, 7.40; N, 9.80; S, 11.14.