Literature DB >> 11169654

Highly Selective Ring-Opening/Cross-Metathesis Reactions of Norbornene Derivatives Using Selenocarbene Complexes as Catalysts This work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture, Japan.

Hiroyuki Katayama1, Hideto Urushima, Tsuneo Nishioka, Chikaya Wada, Masato Nagao, Fumiyuki Ozawa.   

Abstract

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Year:  2000        PMID: 11169654     DOI: 10.1002/1521-3773(20001215)39:24<4513::aid-anie4513>3.0.co;2-c

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


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  5 in total

1.  Enol ethers as substrates for efficient Z- and enantioselective ring-opening/cross-metathesis reactions promoted by stereogenic-at-Mo complexes: utility in chemical synthesis and mechanistic attributes.

Authors:  Miao Yu; Ismail Ibrahem; Masayuki Hasegawa; Richard R Schrock; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2012-01-24       Impact factor: 15.419

2.  Recent Advances in the Stereoselective Synthesis of Tetrahydrofurans.

Authors:  John P Wolfe; Michael B Hay
Journal:  Tetrahedron       Date:  2007-01-08       Impact factor: 2.457

Review 3.  Functional end groups for polymers prepared using ring-opening metathesis polymerization.

Authors:  Stefan Hilf; Andreas F M Kilbinger
Journal:  Nat Chem       Date:  2009-09-23       Impact factor: 24.427

4.  Regioselective Domino Metathesis of Unsymmetrical 7-Oxanorbornenes with Electron-Rich Vinyl Acetate toward Biologically Active Glutamate Analogues.

Authors:  Masato Oikawa; Minoru Ikoma; Makoto Sasaki; Martin B Gill; Geoffrey T Swanson; Keiko Shimamoto; Ryuichi Sakai
Journal:  European J Org Chem       Date:  2009-11-01

5.  Synthesis of High Oxidation State Molybdenum Imido Heteroatom-Substituted Alkylidene Complexes.

Authors:  Erik M Townsend; Stefan M Kilyanek; Richard R Schrock; Peter Müller; Stacey J Smith; Amir H Hoveyda
Journal:  Organometallics       Date:  2013-08-26       Impact factor: 3.876

  5 in total

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