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Search for "tertiary butyl carbamate" in Full Text gives 2 result(s) in Beilstein Journal of Organic Chemistry.

Electrophilic oligodeoxynucleotide synthesis using dM-Dmoc for amino protection

  • Shahien Shahsavari,
  • Dhananjani N. A. M. Eriyagama,
  • Bhaskar Halami,
  • Vagarshak Begoyan,
  • Marina Tanasova,
  • Jinsen Chen and
  • Shiyue Fang

Beilstein J. Org. Chem. 2019, 15, 1116–1128, doi:10.3762/bjoc.15.108

Graphical Abstract
  • protections, which contained a tertiary butyl carbamate moiety, were not completely stable under the acidic conditions needed for de-tritylation in each synthetic cycle. Once the protection was lost, in the coupling step, incoming phosphoramidites would react with the free amino groups, and branched ODNs
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Published 20 May 2019

An expedient and new synthesis of pyrrolo[1,2-b]pyridazine derivatives

  • Rajeshwar Reddy Sagyam,
  • Ravinder Buchikonda,
  • Jaya Prakash Pitta,
  • Himabindu Vurimidi,
  • Pratap Reddy Padi and
  • Mahesh Reddy Ghanta

Beilstein J. Org. Chem. 2009, 5, No. 66, doi:10.3762/bjoc.5.66

Graphical Abstract
  • ; tertiary butyl carbamate; tertiary butyl carbazate; α,β-unsaturated ketone; Introduction Pyrrolopyridazine derivatives have various biological applications [1][2][3][4][5][6][7][8], and their fluorescent properties have been investigated for potential use in sensors, lasers, and semiconductor devices [9
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Published 17 Nov 2009
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