Enantioselective total synthesis of the lignan (+)-Linoxepin

Chemistry - A European Journal

Volumn 20, Issue 51, 2014, Pages 17119-17124

  Tietze, Lutz F ^a   Clerc, Jerome ^a   Biller, Simon ^a   Duefert, Svenia C ^a   Bischoff, Matthias ^a,b  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

Author keywords

Asymmetric hydroboration; Carbopalladation; Lignans; Natural products; Total synthesis

Indexed keywords

ENANTIOSELECTIVITY;

CARBOPALLADATION; HYDROBORATION; LIGNANS; NATURAL PRODUCTS; TOTAL SYNTHESIS;

SYNTHESIS (CHEMICAL);

EID: 84915805260     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201404679     Document Type: Article

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57. The optical rotation is in accord with the data from refs. [6] and [7] but showed a difference when compared with the value found for the isolated (+)-linoxepin (ref. [4]).