1910
DOI: 10.1021/ja01924a012
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Abstract: IKCANIC A S D BIOLOGIC.\I.being soon recognized. Soxhlet especially devoted much of his tinie to the study of the method and established' the exact conditions under which the determination must be carried out in order to get satisfactory results.

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Cited by 7 publications
(8 citation statements)
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References 7 publications
(18 reference statements)
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“…lsoxazolines (23a,b), prepared from cyclopentene or cyclohexene and in situ benzonitrile oxide, were reduced with lithium aluminium hydride (LAH) to the aminoalcohols (24a, b). (83987) The diastereomeric aminoalcohol (25) was prepared by reduction with sodium in ethanol. Aminoalcohols (24b) and (25) were cyclized with imidates to diastereomeric fused-skeleton dihydrooxazines (26a,b) and (27).…”
Section: Arylsubstituted Fusedskeleton Satu-rated 134xazines Isoindmentioning
confidence: 99%
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“…lsoxazolines (23a,b), prepared from cyclopentene or cyclohexene and in situ benzonitrile oxide, were reduced with lithium aluminium hydride (LAH) to the aminoalcohols (24a, b). (83987) The diastereomeric aminoalcohol (25) was prepared by reduction with sodium in ethanol. Aminoalcohols (24b) and (25) were cyclized with imidates to diastereomeric fused-skeleton dihydrooxazines (26a,b) and (27).…”
Section: Arylsubstituted Fusedskeleton Satu-rated 134xazines Isoindmentioning
confidence: 99%
“…(83987) The diastereomeric aminoalcohol (25) was prepared by reduction with sodium in ethanol. Aminoalcohols (24b) and (25) were cyclized with imidates to diastereomeric fused-skeleton dihydrooxazines (26a,b) and (27). With ethyl chloroformate and sodium ethoxide, the 1,3-oxazin-2-ones (28a) and (28b) were prepared, while the corresponding thiones (29a) and (29b) were obtained with carbon disulphide and lead(l1) nitrate.…”
Section: Arylsubstituted Fusedskeleton Satu-rated 134xazines Isoindmentioning
confidence: 99%
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“…In recent years, the synthesis of six membered quinazoline heterocycles and its derivatives Fig. 1 has become attractive in synthetic organic chemistry due to their broad biological and medicinal activities [17][18] [38] are such methods for the preparation of 1,2-dihydroquinazolines. However, these methods suffer from limitations such as, harsh reaction conditions, expensive reagents, difficult purification procedures, lesser product yields, metal catalysts as well as more than stoichiometric amount of reagents.…”
Section: Introductionmentioning
confidence: 99%
“…The NADP/NADPH redox system and diverse alkaloids such as nicotine contain pyridine, a six‐membered heterocycle [10] . Isocoumarins [11,12] and quinazolines [13,14] are known for their excellent biological activities. Some of the important pharmaceutically relevant six‐membered heterocyclic compounds are displayed (Figure 2).…”
Section: Introductionmentioning
confidence: 99%