Bicyclo[3.3.1]Nonanes as Synthetic Intermediates. Vii.(¹) An Intramolecular Alkylation in the Bicyclo[3.3.1]nonan-3-One System by the “fork head” endo-Methanol: An Efficient Route to 4-Protoadamantanone

T. Momose Faculty of Pharmaceutical Sciences, Kinki University, 3-4-1, Kowakae, Higashi-Osaka, Osaka, 577, Japan

T. Itooka Faculty of Pharmaceutical Sciences, Kinki University, 3-4-1, Kowakae, Higashi-Osaka, Osaka, 577, Japan

O. Muraoka Faculty of Pharmaceutical Sciences, Kinki University, 3-4-1, Kowakae, Higashi-Osaka, Osaka, 577, Japan

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Osamu Muraoka, Yalou Wang, Masafumi Okumura, Saori Nishiura, Genzoh Tanabe & Takefumi Momose. (1996) A Facile Synthesis of 7-Methylenebicyclo-[3.3.1]nonan-3-one and its Transformation Leading to the Novel Tricyclic System, Protoadamantane. Synthetic Communications 26:8, pages 1555-1562.
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Ana N. Santiago, Adriana E. Stahl, Gladis L. Rodriguez & Roberto A. Rossi. (1997) Reactions of 1- and 2-Halo- and 1,2-Dichloroadamantanes with Nucleophiles by the S RN 1 Mechanism . The Journal of Organic Chemistry 62:13, pages 4406-4411.
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. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 1085 1229 .

David T. Macpherson & Harshad K. Rami. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 159 214 .

Ashraf N. Abdel-Sayed & Ludwig Bauer. (1988) Syntheses of 1,2-distributed adamantanes. Tetrahedron 44:7, pages 1873-1882.
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Takefumi Momose, Toshiyuki Itooka, Takafumi Nishi, Mari Uchimoto, Keiko Ohnishi & Osamu Muraoka. (1987) Bicyclo[3.3.1]nonanes as synthetic intermediates XIII.. Tetrahedron 43:16, pages 3713-3720.
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T. MOMOSE, T. ITOOKA & O. MURAOKA. (2016) ChemInform Abstract: BICYCLO(3.3.1)NONANES AS SYNTHETIC INTERMEDIATES. VII. AN INTRAMOLECULAR ALKYLATION IN THE BICYCLO(3.3.1)NONAN‐3‐ONE SYSTEM BY THE FORK HEAD ENDO‐METHANOL: AN EFFICIENT ROUTE TO 4‐PROTOADAMANTANONE. Chemischer Informationsdienst 15:43.
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Bicyclo[3.3.1]Nonanes as Synthetic Intermediates. Vii.(¹) An Intramolecular Alkylation in the Bicyclo[3.3.1]nonan-3-One System by the “fork head” endo-Methanol: An Efficient Route to 4-Protoadamantanone

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Bicyclo[3.3.1]Nonanes as Synthetic Intermediates. Vii.(1) An Intramolecular Alkylation in the Bicyclo[3.3.1]nonan-3-One System by the “fork head” endo-Methanol: An Efficient Route to 4-Protoadamantanone

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Bicyclo[3.3.1]Nonanes as Synthetic Intermediates. Vii.(¹) An Intramolecular Alkylation in the Bicyclo[3.3.1]nonan-3-One System by the “fork head” endo-Methanol: An Efficient Route to 4-Protoadamantanone