Development of a double allylboration reagent targeting 1,5-syn-(E)-diols: Application to the synthesis of the C(23)-C(40) fragment of tetrafibricin

Tetrahedron

Volumn 67, Issue 35, 2011, Pages 6497-6512

  Nuhant, Philippe ^a   Kister, Jeremy ^a   Lira, Ricardo ^a   Sorg, Achim ^a   Roush, William R ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

Allene hydroboration; Double allylboration; Kinetically controlled; Stereoselective synthesis of syn 1,5 E diols; Studies on the synthesis of tetrafibricin; Tetrabutylammonium allenyltrifluoroborate

Indexed keywords

1 CYCLOHEXYL 7 PHENYLHEPT 3 ENE 1,5 DIOL; 1,5 DIPHENYLPENT 2 ENE 1,5 DIOL; 1,7 DIPHENYLHEPT 2 ENE 1,5 DIOL; 1,7 DIPHENYLHEPT 3 ENE 1,5 DIOL; 6 (BENZYLOXY) 1 CYCLOHEXYLHEX 2 ENE 1,5 DIOL; ALLENE DERIVATIVE; FIBRINOGEN RECEPTOR ANTAGONIST; TETRABUTYLAMMONIUM; TETRABUTYLAMMONIUM ALLENYLTRIFLUOROBORATE; TETRAFIBRICIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DOUBLE ALLYLBORATION; ENANTIOSELECTIVITY; HYDROBORATION; PRIORITY JOURNAL; SYNTHESIS;

EID: 79960961355     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.06.008     Document Type: Article

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