✦ LIBER ✦

Reactive Maillard intermediates leading to coloured products — 5-hydroxymethyl- and 5-(1,2-dihydroxyethyl)-3(2H)-furanone

✍ Scribed by Markus Lederer; Marcus Glomb; Peter Fischer; Franz Ledl

Book ID: 112497528
Publisher: Springer
Year: 1993
Tongue: English
Weight: 652 KB
Volume: 197
Category: Article
ISSN: 0044-3026
DOI: 10.1007/bf01202608

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

5-Hydroxymethyl-3-(2H)-furanone, 5-(1,2-

5-Hydroxymethyl-3-(2H)-furanone, 5-(1,2-dihydroxyethyl)-3(2H)-furanone and 5-hydroxy-2H-pyran-3(6H)-one: reactive intermediates in the Maillard reaction of hexoses and pentoses

✍ Marcus Glomb; Markus Lederer; Franz Ledl 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 479 KB

Ring contraction products from 2,3-dihyd

Ring contraction products from 2,3-dihydro-3,5-dihydroxy-6-methyl-4(H)-pyran-4-one: 4-hydroxy-5-hydroxymethyl-2-methyl-3(2H)-furanone and 2,5-dimethyl-4-hydroxy-3(2H)-furanone

✍ Mills, Frank D. 📂 Article 📅 1978 🏛 American Chemical Society 🌐 English ⚖ 533 KB

Regio- and stereoselective 1,3-dipolar c

Regio- and stereoselective 1,3-dipolar cycloaddition of arylnitrile oxides to 5-acetoxy-2(5H)-furanone

✍ Peter Oravec; Ľubor Fišera; Roman Gažo 📂 Article 📅 1991 🏛 Springer Vienna 🌐 English ⚖ 387 KB

Glycine Specific Novel Maillard Reaction

Glycine Specific Novel Maillard Reaction Products: 5-Hydroxy-1,3-dimethyl-2(1 H )-quinoxalinone and Related Compounds

✍ Keyhani, Anahita; Yaylayan, Varoujan A. 📂 Article 📅 1997 🏛 American Chemical Society 🌐 English ⚖ 288 KB

A general method for alkylating 2(5H)-fu

A general method for alkylating 2(5H)-furanones; reduction of products to 3-, 2,3-, and 3,4-substituted furans

✍ S.W. Pelletier; Z. Djarmati; S.D. Lajsˇić; I.V. Mic´ovic´; D.T.C. Yang 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 661 KB

Asymmetric 1,4-additions to 5-alkoxy-2(5

Asymmetric 1,4-additions to 5-alkoxy-2(5h)-furanones : An efficient synthesis of (r)- and (s)- 3,4-epoxy-1-butanol

✍ Ben L. Feringa; Ben De Lange 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 765 KB

The synthesis of enantiomerically pure 5-menthyloxy-2(5B)-furanones is described as well as the diastereoselective 1,4-addition of thiols to these butenolides to yield new homochiral CQ-synthons. Kinetic resolution of 5-methoxy-2(5H)-furanone, with an enautiameric excess of 139, wae achieved by cinc