Chemie von a‐Aminonitrilen. Aldomerisierung von Glycolaldehyd‐phosphat zu racemischen Hexose‐2,4,6‐triphosphaten und (in Gegenwart von Formaldehyd) racemischen Pentose‐2,4‐diphosphaten: rac‐Allose‐2,4,6‐triphosphat und rac‐Ribose‐2,4‐diphosphat sind die Reaktionshauptprodukte
- 8 August 1990
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 73 (5) , 1410-1468
- https://doi.org/10.1002/hlca.19900730526
Abstract
No abstract availableKeywords
This publication has 68 references indexed in Scilit:
- Chemie von α‐Aminonitrilen. Aziridin‐2‐carbonitril photochemische Bildung aus 2‐AminopropennitrilHelvetica Chimica Acta, 1990
- Prebiotic ribose synthesis: A critical analysisDiscover Life, 1988
- Carbon-13 NMR studies of [1-13C]aldoses: empirical rules correlating pyranose ring configuration and conformation with carbon-13 chemical shifts and carbon-13/carbon-13 spin couplingsJournal of the American Chemical Society, 1987
- RNA catalysis and the origins of lifeJournal of Theoretical Biology, 1986
- Methylglyoxal synthase uses the trans isomer of triose-1,2-enediol 3-phosphateJournal of the American Chemical Society, 1983
- Synthesis of .alpha.-cyanoglycine N-carboxyanhydride and .alpha.-cyanoglycineThe Journal of Organic Chemistry, 1974
- An Unusual Photochemical Rearrangement in the Synthesis of Adenine from Hydrogen Cyanide1Journal of the American Chemical Society, 1966
- Synthesis of adenine from ammonium cyanideBiochemical and Biophysical Research Communications, 1960
- The Stereochemistry of the Ivanov and Reformatsky Reactions. IJournal of the American Chemical Society, 1957
- Production of Some Organic Compounds under Possible Primitive Earth Conditions1Journal of the American Chemical Society, 1955