Synthesis and reactivity of bicycles derived from tartaric acid and alpha-amino acids: A novel class of conformationally constrained dipeptide isosteres based upon enantiopure 3-aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylicacid. (vol 64, pg 7358, 1995)

Authors
Guarna, A Guidi, A Machetti, F Menchi, G Occhiato, EG Scarpi, D Sisi, S Trabocch, A
Citation
A. Guarna et al., Synthesis and reactivity of bicycles derived from tartaric acid and alpha-amino acids: A novel class of conformationally constrained dipeptide isosteres based upon enantiopure 3-aza-6,8-dioxabicyclo[3.2.1]octane-7-carboxylicacid. (vol 64, pg 7358, 1995), J ORG CHEM, 65(15), 2000, pp. 4782-4782
Citations number
1
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
00223263 → ACNP
Volume
65
Issue
15
Year of publication
2000
Pages
4782 - 4782
Database
ISI
SICI code
0022-3263(20000728)65:15<4782:SAROBD>2.0.ZU;2-G