158091-86-2Relevant academic research and scientific papers
Stereoselectivity of intramolecular cyclisations of nitrones derived from 3-oxahept-6-enals
Gravestock, Michael B.,Knight, David W.,Lovell, Jennifer S.,Thornton, Steven R.
, p. 3143 - 3155 (2007/10/03)
Intramolecular [l,3]-dipolar cycloadditions of nitrones 33, derived from 3-oxahept-6-enals 7, substituted at either the 4- or 5-position and prepared using a variety of approaches, give good to excellent yields of the cycloadducts 34-37, with good levels
Stereoselectivity of Intramolecular Cyclisations of Nitrones Derived from 3-Oxahept-6-enals
Gravestock, Michael B.,Knight, David W.,Lovell, Jennifer S.,Thornton, Steven R.
, p. 1661 - 1664 (2007/10/02)
Intramolecular cycloadditions of the nitrones 9 and 14 show moderate to good stereoselections in favour of the cis-fused diastereoisomers 10 or 16, respectively.
