Addition of HOAt dramatically improves the effectiveness of pentafluorophenyl-based coupling reagents

DOI: 10.1016/S0040-4039(99)00089-1

Source and publish data:

Tetrahedron Letters p. 2045 - 2048 (1999)

Update date:2022-08-16

Topics:

Authors:

Klose Klose

El-Faham

Henklein

Carpino Carpino

Bienert Bienert

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Article abstract of DOI:10.1016/S0040-4039(99)00089-1

In the course of comparing the effectiveness of several HOAt- and HOPfp- derived coupling reagents by cyclization and segment condensation of model sequences, using HPLC to follow the time course and to determine the outcome in terms of oligomerization an

Full text of DOI:10.1016/S0040-4039(99)00089-1

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Article Doi

Addition of HOAt dramatically improves the effectiveness of pentafluorophenyl-based coupling reagents

DOI: 10.1016/S0040-4039(99)00089-1

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(99)00089-1

Full text of DOI:10.1016/S0040-4039(99)00089-1

Products guided by the article

R&D Labs maybe for 164861-48-7

Relevant to this article

Stitching of tyrosine and 10H-acridin-9-one: Turn-ON fluorescence in the narrow pH range 7.4-8.5 and intracellular labelling of cancer cells

C-9 fluorenyl substituted anthracenes: A promising new family of blue luminescent materials

Highly selective aromatization and isomerization of N-alkanes from bimetallic Pt-Zn nanoparticles supported on a uniform aluminosilicate

Synthesis of novel thermally reversible photochromic axially chiral spirooxazines

New Derivatives of Tetrahydroborate(1-), BH3SiF3- and BH2(SiF3)2-

Chemistry of pseudomonic acid. Part 16. Aryl and heteroaryl ketone derivatives of monic acid

New Derivatives of Tetrahydroborate(1-), BH3SiF3^- and BH2(SiF3)2^-