This submission belongs to the session b. Natural Products Chemistry of the event The 14th International Electronic Conference on Synthetic Organic Chemistry
Published date
31 Oct, 2010
Citation
Shirish P. Deshmukh, Dattatraya V. Mangte, Anvita S. Dandale, Per–O–acetyl Lactosyl Isothiourea Derivatives: Synthesis and Antimicrobial Activities, in Proceedings of The 14th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2010, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-14-00423
Share
Email
Facebook
Twitter
LinkedIn
Per–O–acetyl Lactosyl Isothiourea Derivatives: Synthesis and Antimicrobial Activities
Shirish P. Deshmukh 1
Dattatraya V. Mangte 1
Anvita S. Dandale 2
1. P. G. Department of Chemistry, Shri Shivaji College, Akola–444001, MS, India.
2. Dept. of Applied Chemistry, Faculty of Tech. & Engg., The M. S. University of Baroda, Vadodara–390001, Gujarat, India.
Abstract
Glycosyl (iso) thioureas being an important intermediate in the synthesis of thioureido carbohydrates herein we reported the synthesis of per–O–acetyl lactosyl aryl isodithiobiuret derivatives. These compounds were synthesized by nucleophilic addition of per-O-acetyl lactosyl aryl isothiourea to tolyl isothiocyanate. Structures of these compounds were confirmed on the basis of IR, HNMR, Mass spectra and elemental analysis. These compounds were also screened for their in vitro antimicrobial activities against bacteria S. aureus, E. coli, P. vulgaris, P. aeruginosa and fungi A. niger, Penicillium.
Keywords
Lactosyl isothioureas
isodithiobiurets
Synthesis
Antibacterial
Antifungal activity
Tuning of a MISPE procedure for the simultaneous extraction of Dexamethasone and Betamethasone
Disazo symmetrical stilbene dyes. Synthesis and colour evaluation.