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Details
SASRIN™ (=Super Acid Sensitive ResIN) was developed in our own laboratories especially for Fmoc solid phase synthesis (EP 0 292 729, US 4,831,084 and US 4,914,151). Its high acid lability enables the cleavage and isolation of the protected peptide fragment.
Beside SPPS SASRIN™ has been used in several organic reactions like the synthesis of 4-aryl substituted β-lactams employing Suzuki and Heck couplings, the synthesis of β-sultams, quinazoline-2,4-diones, pyridines and pyrido[2,3-d]pyrimidines and the generation of secondary alkylamines by borane reduction. S.S.Rahman et al. reported on the FT-IR and Raman spectroscopic monitoring of reactions on a single SASRIN™ bead and C.L.Brummel et al. on the evaluation of mass spectrometric methods applicable to the direct analysis of non-peptide bead-bound combinatorial libraries.
For a review on the manifold applications of our SASRIN™ resin, including many useful procedures, please ask for our SASRIN™ brochure.
Catalog Number
D-1295
Synonyms
3-CH₃O-4-HOCH₂-Ph-O-CH₂-Ph-polymer
Molecular Formula
n/a
Relative Molecular Mass
n/a
CAS Registry Number
124760-64-1
Storage Conditions
+5 ± 3 °C
Links / Documents:
Brochures:
Bachem product citations
A.A.Profit et al.,
J. Am. Chem. Soc.,
121,
280 (1999)
Product citations
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Chimia,
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S.S.Rahmann et al.,
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63,
6196 (1998)
B.Ruhland et al.,
J. Org. Chem.,
62,
7820 (1997)
M.F.Gordeev et al.,
Tetrahedron Lett.,
38,
1729 (1997)
M.Mergler et al.,
Peptides, Chemistry and Biology, Proceedings of the 10th American Peptide Symposium, St. Louis, p. 259, G.R.Marshall, ed., Escom, Leiden,
(1988)
M.Mergler et al.,
Tetrahedron Lett.,
29,
4005 (1988)
M.Mergler et al.,
Tetrahedron Lett.,
29,
4009 (1988)
