![Sample our Physical Sciences journals, sign in here to start your FREE access for 14 days]({"type":"image" , "src" : "/sda/110819/TOC-Subject-Sample-2021-Physical-Sciences.jpg"})
Abstract
Meldrum's acid (1) on bisacylation with succinyl chloride afforded a neutral diketo product (2); however, the dimer enolic products (3) with acidic nature resulted in glutaryl and adipyl dichlorides. Monoacylation of (1) with acetyl chloride gave acidic 5‐acetyl Meldrum's acid (4) in enol form.
Presented at the National Symposium on Newer Concepts in Organic Synthesis, 1998, Aurangabad, India, [Abstract: 1.29].
This paper is dedicated to Prof. M. M. Salunkhe, Vice-Chancellor, Shivaji University, Kolhapur–416 004 (Former Director, Institute of Science, Mumbai – 400 032) India.
Keywords:
Acknowledgment
We thank the University Grants Commission, New Delhi, India, for financial assistance.
Notes
Presented at the National Symposium on Newer Concepts in Organic Synthesis, 1998, Aurangabad, India, [Abstract: 1.29].
This paper is dedicated to Prof. M. M. Salunkhe, Vice-Chancellor, Shivaji University, Kolhapur–416 004 (Former Director, Institute of Science, Mumbai – 400 032) India.