## Abstract The direct conversion of indole to indole‐3‐acetic acid without tryptophan as an intermediate has previously been shown to occur __in vivo__, as well as __in vitro__, with seedlings of plants. In order to facilitate the purification of the enzymes that carry out the enzymatic synthesis
Synthesis of the β-D-glucosyl ester of [carbonyl-13C]-indole-3-acetic acid
✍ Scribed by Andreja Jakas; Volker Magnus; Stefica Horvat; Göran Sandberg
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 339 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
An efficient, operationally simple synthetic approach to 1‐O‐([carbonyl‐^13^C]‐indole‐3′‐ylacetyl)‐β‐D‐glucopyranose is described. The synthesis was carried out by fusing a fully benzylated 1‐O‐glucosylpseudourea intermediate with [carbonyl‐^13^C]‐indole‐3‐acetic acid, followed by hydrogenolytic removal of the protective groups.
📜 SIMILAR VOLUMES
## Abstract Deuterium Labelled 5‐hydroxyindole‐3‐acetic acid and 5‐hydroxy‐tryptamine have been sythesized by a modification of the procedure previously described by Ek and Witkop (9) for the nondeuterated analogues. The deuterium is introduced by a solvent exahange reaction and by reduction with l
## Abstract The syntheses of two perdeuterated ionic liquids (ILs), which have found use as solvents for cellulose derivatization and processing in addition, are described: 1‐ethyl‐3‐methylimidazolium acetate (EMIM‐OAc‐d~14~) and 1‐butyl–3‐methylimidazolium acetate (BMIM‐OAc‐d~18~). The targets wer