Literature DB >> 18811204

A synthesis of (-)-mintlactone.

Roderick W Bates1, S Sridhar.   

Abstract

Mintlactone is synthesized in a concise and efficient way by using a highly diastereoselective intramolecular propargylic Barbier reaction, followed by an allenol cyclocarbonylation. Tin(II) chloride is found to be the most effective reagent for the Barbier reaction.

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Year:  2008        PMID： 18811204     DOI： 10.1021/jo801433f

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  4 in total

1.  Convergent route to the spirohexenolide macrocycle.

Authors:  Brian D Jones; James J La Clair; Curtis E Moore; Arnold L Rheingold; Michael D Burkart
Journal:  Org Lett       Date:  2010-10-15       Impact factor: 6.005

2.  Synthesis and Characterization of Bimetallic Nanoclusters Stabilized by Chiral and Achiral Polyvinylpyrrolidinones. Catalytic C(sp3)-H Oxidation.

Authors:  Huafang Fan; Zongbo Tong; Zhaoyang Ren; Kanchan Mishra; Shunya Morita; Edruce Edouarzin; Lingaraju Gorla; Boris Averkiev; Victor W Day; Duy H Hua
Journal:  J Org Chem       Date:  2022-05-05       Impact factor: 4.198

Review 3.  Application of Pauson-Khand reaction in the total synthesis of terpenes.

Authors:  Majid M Heravi; Leila Mohammadi
Journal:  RSC Adv       Date:  2021-11-29       Impact factor: 4.036

Review 4.  Copper-catalyzed enantioselective conjugate addition of organometallic reagents to challenging Michael acceptors.

Authors:  Delphine Pichon; Jennifer Morvan; Christophe Crévisy; Marc Mauduit
Journal:  Beilstein J Org Chem       Date:  2020-02-17       Impact factor: 2.883
  4 in total

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