Literature DB >> 12227822

An efficient synthesis of novel carbocyclic nucleosides with use of ring-closing metathesis from D-lactose.

Joon Hee Hong1, Myung Jung Shim, Bong Oh Ro, Ok Hyun Ko.   

Abstract

This paper describes an efficient synthetic route for various types of novel carbocyclic nucleosides. The required stereochemistry of the targeted nucleosides was successfully obtained with use of Grubbs cyclization and Trost allylic alkylation from the carbohydrate chiral template "D-lactose".

Entities:  

Year:  2002        PMID: 12227822     DOI: 10.1021/jo0202536

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


  1 in total

1.  A greener enantioselective synthesis of the antiviral agent North-methanocarbathymidine (N-MCT) from 2-deoxy-d-ribose.

Authors:  Olaf R Ludek; Victor E Marquez
Journal:  Tetrahedron       Date:  2009-10-10       Impact factor: 2.457

  1 in total

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