✦ LIBER ✦

Two Novel β-Carboline Compounds from the Maillard Reaction between Xylose and Tryptophan

✍ Scribed by Wang, Mingfu; Jin, Yi; Li, Jiangang; Ho, Chi-Tang

Book ID: 118745112
Publisher: American Chemical Society
Year: 1999
Tongue: English
Weight: 53 KB
Volume: 47
Category: Article
ISSN: 0021-8561
DOI: 10.1021/jf980804m

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

New Colored Compounds from the Maillard

New Colored Compounds from the Maillard Reaction between Xylose and Lysine

✍ Arnoldi, Anna; Corain, Emanuela A.; Scaglioni, Leonardo; Ames, Jennifer M. 📂 Article 📅 1997 🏛 American Chemical Society 🌐 English ⚖ 287 KB

Methylglyoxal-derived β-carbolines forme

Methylglyoxal-derived β-carbolines formed from tryptophan and its derivates in the Maillard reaction

✍ I. Nemet; L. Varga-Defterdarović 📂 Article 📅 2006 🏛 Springer 🌐 English ⚖ 84 KB

Origin of carbons in sulfur-containing a

Origin of carbons in sulfur-containing aroma compounds from the Maillard reaction of xylose, cysteine and thiamine

✍ Christoph Cerny 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 199 KB

Novel formation of phenylcyclopropanes f

Novel formation of phenylcyclopropanes from the reaction of β-cyanostyrenes and related compounds with 2-methoxyfuran: experimental and theoretical studies

✍ Itoh, Kuniaki; Kishimoto, Shigehisa 📂 Article 📅 2009 🏛 Royal Society of Chemistry 🌐 English ⚖ 899 KB

Two novel Diels-Alder reaction-type dime

Two novel Diels-Alder reaction-type dimeric pinguisane sesquiterpenoids and related compounds from the liverwort Porella acutifolia subsp. tosana

✍ Toshihiro Hashimoto; Hiroshi Irita; Masami Tanaka; Shigeru Takaoka; Yoshinori As 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 248 KB

From the ether extract of the liverwort Porella acutifolia subsp, tosana, two new pinguisanetype and two novel Diels-AIder reaction-type dimeric pinguisane sesquiterpenoids have been isolated. Their absolute structures were determined by a combination of 2D-NMR and CD spectra, X-ray crystallographic

Novel synthesis of stable 1,5-diionic or

Novel synthesis of stable 1,5-diionic organophosphorus compounds from the reaction between triphenylphosphine and acetylenedicarboxylic acid in the presence of N–H heterocyclic compounds

✍ Morteza Ziyaadini, Malek Taher Maghsoodlou, Nourallah Hazeri, Sayyed Mostafa Hab 📂 Article 📅 2012 🏛 Springer Vienna 🌐 English ⚖ 294 KB