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Featured researches published by M. Ohashi.


Tetrahedron | 1965

Alkaloids studies—LIII: The structures of nine new alkaloids from Aspidosperma dasycarpon A. DC.

J. A. Joule; M. Ohashi; B. Gilbert; Carl Djerassi

Abstract The structures of twelve alkaloids (I–XII) isolated from Aspidosperma dasycarpon A. DC. are deduced. Nine of these indole alkaloids are new.


Tetrahedron | 1964

Mass spectrometry in structural and stereochemical problems—XXXIX : Tropane alkaloids☆☆☆

E.C. Blossey; H. Budzikiewicz; M. Ohashi; G. Fodor; Carl Djerassi

Abstract The mass spectra of a series of tropane alkaloids have been measured and the major fragments identified, largely through the use of deuterium or substituent labelling. The principal bond fissions follow the paths laid down earlier for simple amines, cyclic ketones and alcohols, thus affording characteristic fragmentation patterns, which may prove useful in the characterization of unknown members of this class.


Tetrahedron | 1963

Mass spectrometry in structural and Stereochemical problems—XXXIV : Aromatic methyl and ethyl ethers☆☆☆

Z. Pelah; J. M. Wilson; M. Ohashi; H. Budzikiewicz; Carl Djerassi

Abstract The behavior under electron impact of a series of aromatic methoxy and ethoxy compounds has been observed. The more common fragmentation processes are interpreted and in some cases the differences among spectra of positional isomers can be explained.


Tetrahedron | 1963

Mass spectrometry in structural and Stereochemical problems—XXXVI : Alkaloids of periwinkles—27; the mass spectra of stereo-isomers of the sarpagine-akuammidine group

M. Ohashi; H. Budzikiewicz; J. M. Wilson; Carl Djerassi; J. Lévy; J. Gosset; Jean LeMen; Maurice-Marie Janot

Abstract Mass spectra have been measured of members of the sarpagine-akuammidine group differing in stereochemistry at C-16. Attention is called to possible fallacies in expecting analogous fragmentation behavior of closely related compounds (N (a) —H vs. N (a) —Me) if the mechanism of a specific fragmentation is not known. Attention is drawn to the structural information which can be gained from thermal decomposition processes prior to electron impact. The mutual advantages of an all-glass and a direct inlet system are discussed.


Tetrahedron | 1963

Mass spectrometry in structural and stereochemical problems—XXXIII : Colchicine alkaloids

J. M. Wilson; M. Ohashi; H. Budzikiewicz; F. Šantavý; Carl Djerassi

Abstract Mass spectra have been measured for a series of colchicine alkaloids and correlations between spectra and structure have been made. The results indicate that mass spectra will be of assistance in structure determination of such naturally occurring tropolones.


Tetrahedron | 1963

Mass spectrometry in structural and stereochemical problems—XXXVII. : Tropone and tropolone derivatives☆☆☆★

J. M. Wilson; M. Ohashi; H. Budzikiewicz; Carl Djerassi; Shô Itô; Tetsuo Nozoe

Abstract The general observation is made that on electron impact the molecular ions of tropone derivatives eliminate carbon monoxide as a neutral molecule and the resultant ions behave as benzene derivatives. Exceptions from this rule can be explained in terms of the presence of specific structural features.


Cellular and Molecular Life Sciences | 1964

The structures of five newAspidosperma alkaloids related to uleine

M. Ohashi; J. A. Joule; B. Gilbert; Carl Djerassi

Aus der Rinde des brasilianischen BaumesAspidosperma dasycarpon A. DC. wurden fünf neue Alkaloide (II–VI) isoliert, die das selten vorkommende Uleinskelett besitzen. Die Strukturen wurden durch chemische Korrelation mit Ulein (I) sichergestellt.


Journal of the American Chemical Society | 1963

Mass Spectrometry in Structural and Stereochemical Problems. XXXI.1 Aporphines and Related Alkaloids2

M. Ohashi; J. M. Wilson; H. Budzikiewicz; W. A. Slusarchyk; Carl Djerassi


Acta Chemica Scandinavica | 1963

Mass Spectra of Isothiocyanates.

Anders Kjaer; M. Ohashi; J. M. Wilson; Carl Djerassi; Jon Munch-Petersen


Tetrahedron Letters | 1964

Alkaloid studies LI. The structure of aspidodasycarpine.

M. Ohashi; J. A. Joule; Carl Djerassi

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G. Fodor

Hungarian Academy of Sciences

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