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benzhydrylamine

Known as: 1,1-diphenylmethylamine 
National Institutes of Health

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1 relation

Broader (1)

Benzhydryl Compounds

Papers overview

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2017
2017
Highly Stereoselective Strecker Synthesis Induced by a Slight Modification of Benzhydrylamine from Achiral to Chiral.
2-Methylbenzhydrylamine is a chiral variant of achiral benzhydrylamine; however, the chirality formed from the small difference… 
2009
2009
Synthesis of neuropeptide Y.
Neuropeptide Y (NPY), a hexatriacontapeptide amide, was synthesized on benzhydrylamine resin. The peptide product obtained by HF… 
2009
2009
Solid-phase synthesis of porcine vasoactive intestinal peptide.
The 28-residue sequence of porcine vasoactive peptide (VIP) was assembled on a benzhydrylamine resin support, cleaved by HF… 
Highly Cited
2000
Highly Cited
2000
An Ammonia Equivalent for the Dimethyltitanocene-Catalyzed Intermolecular Hydroamination of Alkynes.
Commercially available alpha-aminodiphenylmethane 1 (benzhydrylamine) serves as a convenient ammonia equivalent in the… 
1993
1993
Comparative multiple synthesis of fifty linear peptides: evaluation of cotton carrier vs. T bag-benzhydrylamine resin.
Parallel simultaneous synthesis of fifty linear peptides has been carried out in order to compare in detail two promising… 
1985
1985
Epitopes of the 44-68 human parathyroid hormone fragments: the importance of specific hydrophilic peptide sequences.
1984
1984
Synthesis, conformational studies and biological activities of VIP and related fragments
Highly Cited
1981
Highly Cited
1981
A p-methylbenzhydrylamine resin for improved solid-phase synthesis of peptide amides
1977
1977
Concept of internal structural controls for evaluation of inactive synthetic peptide analogs: synthesis of [Orn13,14]apamin and its guanidination to an apamin derivative with full neurotoxic activity…
The importance of arginine residues 13 and 14 in the bee venom neurotoxin, apamin, was teste by the synthesis of replacement… 
Highly Cited
1974
Highly Cited
1974
Preparation and use of benzhydrylamine polymers in peptide synthesis. II. Syntheses of thyrotropin releasing hormone, thyrocalcitonin 26-32, and eledoisin.
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