Literature DB >> 11270326

From 6-t-butylfulvene to highly functionalized five-membered rings.

J Baumgartner1, H Weber.   

Abstract

6-t-Butylfulvene was used as the starting material for asymmetric dihydroxylation. The obtained protected diol (2) was used for several stereoselective functionalizations such as epoxidations, hydroboration, and aminohydroxylation. However, these fulvene derivatives proved to be rather unreactive and gave no conversion under, e.g., palladium (0), catalyses or hydroboration conditions.

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Year:  2001        PMID: 11270326     DOI: 10.1002/1520-636X(2001)13:3<159::AID-CHIR1014>3.0.CO;2-O

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  1 in total

1.  Diverse modes of reactivity of 6-(chloromethyl)-6-methylfulvene.

Authors:  Ihsan Erden; Scott Gronert; Gabriel Cabrera; Necdet Coskun; Marco Tapken
Journal:  European J Org Chem       Date:  2017-05-26
  1 in total

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