Enantioselective synthesis of cyclic allylboronates by Mo-catalyzed asymmetric ring-closing metathesis (ARCM). A one-pot protocol for net catalytic enantioselective cross metathesis

Tetrahedron

Volumn 60, Issue 34, 2004, Pages 7345-7351

  Jernelius, Jesper A ^a   Schrock, Richard R ^b   Hoveyda, Amir H ^a  

^a BOSTON COLLEGE   (United States)

^b MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

Allylboronates; Asymmetric cross metathesis; Asymmetric ring closing metathesis

Indexed keywords

ALDEHYDE; BORONIC ACID DERIVATIVE; CARBON; MOLYBDENUM;

CATALYSIS; CATALYST; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CHIRALITY; CONFERENCE PAPER; DIASTEREOISOMER; ENANTIOSELECTIVITY; PRIORITY JOURNAL; RING CLOSING METATHESIS; SYNTHESIS;

EID: 3342927719     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.06.017     Document Type: Conference Paper

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37. 3): δ 5.61 (s, 1H), 5.10-4.86 (m, 2H), 4.79 (s, 1H), 4.23-4.18 (m, 1H), 1.90-1.83 (m, 1H), 1.76-1.68 (m, 1H), 1.62 (s, 3H), 1.58 (s, 3H)