@article { ISI:000227615900006,
	title = {Microwave assisted rapid synthesis of 4-amino-3,4-dihydroquinolin-2-ones from azetidin-2-ones},
	journal = {Arkivoc},
	number = {1},
	year = {2005},
	month = {JAN},
	pages = {53-64},
	publisher = {ARKAT USA INC},
	type = {Article},
	address = {C/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USA},
	abstract = {<p>An efficient one-pot synthesis of 4-amino-3,4-dihydroquinolin-2-ones from 3-(2-nitrophenyl)-1, 4-disubstituted azetidin-2-ones is described. Microwave assisted transfer hydrogenation of a nitro group followed by in situ beta-lactam ring opening by the newly formed amino group is the key step in this synthesis.</p>},
	keywords = {4-amino-3, 4-dihydroquinolin-2-ones, azetidin-2-ones, imines, ketenes, Microwave, transfer hydrogenation},
	doi = {10.3998/ark.5550190.0006.106},
	author = {Shirode, N. M. and Kulkarni, K. C. and Gumaste, V. K. and Deshmukh, A. R. A. S.}
}
@article { ISI:000237126200040,
	title = {4-Formylazetidin-2-ones, synthon for the synthesis of (2R,3S) and (2S,3R)-3-amino-2-hydroxydecanoic acid (AHDA)},
	journal = {Tetrahedron},
	volume = {62},
	number = {18},
	year = {2006},
	month = {MAY},
	pages = {4615-4621},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of 3-amino-2-hydroxydecanoic acid (AHDA), a nonproteinogenic amino acid, using enantiopure 3-benzyloxy-4-formylazetidin-2-one as a building block is described. Both the enantiomers of AHDA have been synthesized from the corresponding enantiomer of 3-benzyloxy-4-formylazetidin-2-one in good yield and optical purity. (c) 2006 Published by Elsevier Ltd.</p>},
	keywords = {Amino acids, azetidin-2-ones, Staudinger reaction, stereoselective synthesis, Wittig reaction},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2006.01.082},
	author = {Shirode, N. M. and Deshmukh, A. R. A. S.}
}
