TY - JOUR
T1 - A new method for the generation of α-nitrosoolefins from ketooximes and its application to the synthesis of 5,6-dihydro-4H-1,2-oxazine derivatives [1]
AU - Gaonkar, S. L.
AU - Rai, K. M.Lokanatha
PY - 2005/7
Y1 - 2005/7
N2 - Reaction of ketooximes containing α-methylene group with chloramine-T followed by treatment with triethylamine leads to the formation of α-nitrosoolefins via α-nitrosochloride, which can react in situ intermolecularly with olefinic compounds to produce 5,6-dihydro-4H-1,2-oxazine derivatives in good yield.
AB - Reaction of ketooximes containing α-methylene group with chloramine-T followed by treatment with triethylamine leads to the formation of α-nitrosoolefins via α-nitrosochloride, which can react in situ intermolecularly with olefinic compounds to produce 5,6-dihydro-4H-1,2-oxazine derivatives in good yield.
UR - https://www.scopus.com/pages/publications/22244465196
UR - https://www.scopus.com/inward/citedby.url?scp=22244465196&partnerID=8YFLogxK
U2 - 10.1002/jhet.5570420520
DO - 10.1002/jhet.5570420520
M3 - Article
AN - SCOPUS:22244465196
SN - 0022-152X
VL - 42
SP - 877
EP - 881
JO - Journal of Heterocyclic Chemistry
JF - Journal of Heterocyclic Chemistry
IS - 5
ER -