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Russian Chemical Reviews, 1970, Volume 39, Issue 1, Pages 58–69
DOI: https://doi.org/10.1070/RC1970v039n01ABEH001911
(Mi rcr2327)
 

This article is cited in 4 scientific papers (total in 4 papers)

Detritylation and Transtritylation Reactions

P. Buckus

Vilnius State Pedagogical Institute
English full-text Citations (4)
Abstract: This review deals with various reactions involving the cleavage and certain interesting rearrangements of trityl compounds and the use of trityl protecting groups in the synthesis and reactions of glycerides, carbohydrates, nucleosides, nucleotides, and peptides. The lability of the bond between the trityl group and oxygen, sulphur, nitrogen, carbon, and other atoms has been demonstrated.
The bibliography includes 519 references.
Russian version:
Uspekhi Khimii, 1970, Volume 39, Issue 1, Pages 112–129
DOI: https://doi.org/10.1070/RC1970v039n01ABEH001911
Bibliographic databases:
Document Type: Article
UDC: 547.632.2
Language: English
Original paper language: Russian


Citation: P. Buckus, “Detritylation and Transtritylation Reactions”, Usp. Khim., 39:1 (1970), 112–129; Russian Chem. Reviews, 39:1 (1970), 58–69
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  • https://www.mathnet.ru/eng/rcr2327
  • https://doi.org/10.1070/RC1970v039n01ABEH001911
  • https://www.mathnet.ru/eng/rcr/v39/i1/p112
  • This publication is cited in the following 4 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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