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Nitroxides XXX: sign of a long-range coupling in a bicyclic nitroxide radical
Nitroxides XXX: sign of a long-range coupling in a bicyclic nitroxide radical
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Nitroxides XXX: sign of a long-range coupling in a bicyclic nitroxide radical

Lemaire, H. ; Rassat, A. ; Rey, P.

Chemical physics letters, 1968-12, Vol.2 (8), p.573-574 [Periódico revisado por pares]

Elsevier B.V

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2
Experimental studies of thermal denaturation of the Na-DNA system with respect to manning's model
Experimental studies of thermal denaturation of the Na-DNA system with respect to manning's model
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Experimental studies of thermal denaturation of the Na-DNA system with respect to manning's model

Rix-Montel, Marie-Agnès ; Grassi, Henri ; Vasilescu, Dane

Biophysical chemistry, 1974-10, Vol.2 (3), p.278-289 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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3
The Reaction of Aspartyl Dipeptide Esters with Ketones
The Reaction of Aspartyl Dipeptide Esters with Ketones
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The Reaction of Aspartyl Dipeptide Esters with Ketones

Ariyoshi, Yasuo ; Sato, Naotake

Bulletin of the Chemical Society of Japan, 1972-07, Vol.45 (7), p.2015-2018 [Periódico revisado por pares]

Tokyo: The Chemical Society of Japan

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4
The determination of uranium and thorium in rocks by neutron activation analysis
The determination of uranium and thorium in rocks by neutron activation analysis
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The determination of uranium and thorium in rocks by neutron activation analysis

Morgan, J.W. ; Lovering, J.F.

Analytica chimica acta, 1963-01, Vol.28, p.405-417 [Periódico revisado por pares]

Elsevier B.V

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5
Synthesis of Nitrogen-containing Heterocyclic Compounds through Nitrilium Salt. I. Reaction of Nitriles with 2-(α-Hydroxymethyl, -ethyl, and -isopropyl) cyclohexanol in the Presence of Acid
Synthesis of Nitrogen-containing Heterocyclic Compounds through Nitrilium Salt. I. Reaction of Nitriles with 2-(α-Hydroxymethyl, -ethyl, and -isopropyl) cyclohexanol in the Presence of Acid
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Synthesis of Nitrogen-containing Heterocyclic Compounds through Nitrilium Salt. I. Reaction of Nitriles with 2-(α-Hydroxymethyl, -ethyl, and -isopropyl) cyclohexanol in the Presence of Acid

OHKI, SADAO ; YOSHINO, MOTOYO

Chemical and Pharmaceutical Bulletin, 1969/10/25, Vol.17(10), pp.2142-2150 [Periódico revisado por pares]

The Pharmaceutical Society of Japan

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6
The identity of piptamine and ormosanine, and the structures of ormojanine, ormosinine and panamine
The identity of piptamine and ormosanine, and the structures of ormojanine, ormosinine and panamine
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The identity of piptamine and ormosanine, and the structures of ormojanine, ormosinine and panamine

Wilson, E.M.

Tetrahedron, 1965-01, Vol.21 (9), p.2561-2571 [Periódico revisado por pares]

England: Elsevier Ltd

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7
Accurate Determination of Hydrogen Positions in NH4Cl by Electron Diffraction
Accurate Determination of Hydrogen Positions in NH4Cl by Electron Diffraction
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Accurate Determination of Hydrogen Positions in NH4Cl by Electron Diffraction

Kuwabara, Shigeya

Journal of the Physical Society of Japan, 1959-01, Vol.14 (9), p.1205 [Periódico revisado por pares]

Tokyo: The Physical Society of Japan

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8
Reaction of Some Steroidal Amides and Unsaturated Lactams with Nitrous Acid
Reaction of Some Steroidal Amides and Unsaturated Lactams with Nitrous Acid
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Reaction of Some Steroidal Amides and Unsaturated Lactams with Nitrous Acid

KOBAYASHI, MASARU ; MITSUHASHI, HIROSHI

Chemical and Pharmaceutical Bulletin, 1973/05/25, Vol.21(5), pp.1069-1075 [Periódico revisado por pares]

Tokyo: The Pharmaceutical Society of Japan

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9
Microwave Studies of Collision-Induced Transitions between Rotational Levels. V. “Selection Rules” in NH3–Rare-Gas Collisions
Microwave Studies of Collision-Induced Transitions between Rotational Levels. V. “Selection Rules” in NH3–Rare-Gas Collisions
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Microwave Studies of Collision-Induced Transitions between Rotational Levels. V. “Selection Rules” in NH3–Rare-Gas Collisions

Oka, Takeshi

The Journal of chemical physics, 1968-10, Vol.49 (7), p.3135-3145 [Periódico revisado por pares]

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10
Transformation of quinine into the indole alkaloids—I : The absolute configuration of hunterburnine α- and β-methochloride
Transformation of quinine into the indole alkaloids—I : The absolute configuration of hunterburnine α- and β-methochloride
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Transformation of quinine into the indole alkaloids—I : The absolute configuration of hunterburnine α- and β-methochloride

Sawa, Y.K. ; Matsumura, H.

Tetrahedron, 1969-01, Vol.25 (21), p.5319-5328 [Periódico revisado por pares]

England: Elsevier Ltd

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