## Abstract 1‐O‐ and 5‐O‐Methyl‐^14^C‐myo‐inositols (methyf‐^14^C‐bornesitol and ‐sequoyitol) were synthesized by methylation of appropriately blocked myo‐inositol derivatives with methyl = ^14^C iodide and potassium hydroxide. The benzyl blocking groups of 1‐O‐methyl‐^14^C‐3,4,5, 6‐tetra‐O‐benzyl‐
Synthesis of 14C-indole-3-acetyl-myo-inositol
✍ Scribed by Janusz Nowacki; Jerry D. Cohen; Robert S. Bandurski
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- French
- Weight
- 201 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
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## Abstract Labeled 1‐tryptophan is converted to indole‐3‐acetamide and then to indole‐3‐acetic acid by enzymes from __Pseudomonas savastanoi__. Labeled indole‐3‐acetic acid can be converted to indole‐3‐acetyl‐1‐__0__‐β‐D‐glucose and to indole‐3‐acetyl‐__myo__‐inositol by enzymes from kernels of __
## Abstract The synthesis of indole‐3‐acetyl‐2‐^14^C‐N‐aspartic acid from carrier‐free indole‐3‐acetic acid‐2‐^14^C (54.5 mCi/mmole) and bis‐t‐butyl‐l‐aspartic acid was accomplished by coupling with dicyclohexylcarbodiimide followed by removal of the ester blocking groups by treatment with 2 N NaOH