✦ LIBER ✦

Degradation of alachlor by a soil fungus, Chaetomium globosum

✍ Scribed by Tiedje, James M.; Hagedorn, Myrna L.

Book ID: 125535793
Publisher: American Chemical Society
Year: 1975
Tongue: English
Weight: 649 KB
Volume: 23
Category: Article
ISSN: 0021-8561
DOI: 10.1021/jf60197a029

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Chaetomium globosum, a non-toxic fungus:

Chaetomium globosum, a non-toxic fungus: A potential source of protein (SCP)

✍ S.S. Kahlon; K.L. Kalra 📂 Article 📅 1986 🏛 Elsevier Science ⚖ 282 KB

Metabolism of two new acylanilide herbic

Metabolism of two new acylanilide herbicides, Antor herbicide (H-22234) and Dual (metolachlor) by the soil fungus Chaetomium globosum

✍ McGahen, Linda L.; Tiedje, James M. 📂 Article 📅 1978 🏛 American Chemical Society 🌐 English ⚖ 723 KB

Production of lethal mutations in the fu

Production of lethal mutations in the fungus Chætomium globosum by monochromatic ultra-violet irradiation

✍ Mcaulay, A L; Ford, J M; Dobie, D L 📂 Article 📅 1949 🏛 Nature Publishing Group 🌐 English ⚖ 146 KB

A New Dihydroxanthenone from a Plant-Ass

A New Dihydroxanthenone from a Plant-Associated Strain of the Fungus Chaetomium globosum Demonstrates Anticancer Activity.

✍ E. M. Kithsiri Wijeratne; Thomas J. Turbyville; Anne Fritz; Luke Whitesell; A. A 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 17 KB

Synthesis of β-linked glucosaccharides b

Synthesis of β-linked glucosaccharides by extracts of Chaetomium globosum

✍ H.W. Buston; A. Jabbar 📂 Article 📅 1954 🏛 Elsevier Science ⚖ 489 KB

11- and 4′-Epimers of Chaetomugilin A, N

11- and 4′-Epimers of Chaetomugilin A, Novel Cytostatic Metabolites from Marine Fish-Derived Fungus Chaetomium globosum

✍ Yasuhide Muroga; Takeshi Yamada; Atsushi Numata; Reiko Tanaka 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 German ⚖ 193 KB

## Abstract 11‐ and 4′‐epichaetomugilin A were isolated from a strain of __Chaetomium globosum__ that was originally isolated from the marine fish __Mugil cephalus.__ 11‐Epichaetomugilin A is the first compound to have an opposite absolute configuration at C(11) to that of other azaphilones isolate