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電子書籍・電子雑誌Chemistry letters
Volume number51 (7)
Studies fo...

Studies for absolute configuration of chiral 2,6-cuneanedicarboxylic acid esters

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Studies for absolute configuration of chiral 2,6-cuneanedicarboxylic acid esters

Persistent ID (NDL)
info:ndljp/pid/12998992
Material type
記事
Author
Hiyori Takebeほか
Publisher
The Chemical Society of Japan
Publication date
2022-05-13
Material Format
Digital
Journal name
Chemistry letters 51(7)
Publication Page
-
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コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他(Provided by: CiNii Research)

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Digital

Material Type
記事
Author/Editor
Hiyori Takebe
Atsuya Muranaka
Masanobu Uchiyama
Publication, Distribution, etc.
Publication Date
2022-05-13
Publication Date (W3CDTF)
2022-05-13
Periodical title
Chemistry letters
No. or year of volume/issue
51(7)
Volume
51(7)
ISSN (Periodical Title)
1348-0715
ISSN-L (Periodical Title)
0366-7022
Text Language Code
eng
Persistent ID (NDL)
info:ndljp/pid/12998992
Collection (Materials For Handicapped People:1)
Collection (particular)
国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
Acquisition Basis
オンライン資料収集制度
Date Accepted (W3CDTF)
2023-09-27T16:20:01+09:00
Date Captured (W3CDTF)
2023-09-11
Format (IMT)
application/pdf
Access Restrictions
国立国会図書館内限定公開
Service for the Digitized Contents Transmission Service
図書館・個人送信対象外
Availability of remote photoduplication service
Periodical Title (Persistent ID (NDL))
info:ndljp/pid/12998987
Data Provider (Database)
国立国会図書館 : 国立国会図書館デジタルコレクション

Digital

Summary, etc.
コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
Is Referenced By
How to Set the “Chirality” of Polyhedral Small Molecule Hydrocarbons: Decoration and Editing of Cubane Skeleton
Scaffold Editing of Cubanes into Homocubanes, Homocuneanes via Cuneanes
Catalytic Asymmetric Synthesis of 2,6‐Disubstituted Cuneanes through Enantioselective Constitutional Isomerization of 1,4‐Disubstituted Cubanes
Directed Metalation of 1-Cuneanecarboxamide: Simple Route to 1,2-Disubstituted Cuneanes
Biological Evaluation of Isosteric Applicability of 1,3‐Substituted Cuneanes as <i>m</i>‐Substituted Benzenes Enabled by Selective Isomerization of 1,4‐Substituted Cubanes
Cuneanes as Potential Benzene Bioisosteres Having Chirality
Constitutional isomerization of cubane to semibullvalene via cuneane in hot water
光学活性かご型炭化水素分子群の網羅的合成—キュバンScaffold Editing—
かご型炭化水素キュバン・クネアンの創薬応用を志向した精密有機合成化学
References
Silver(I)- and palladium(II)-catalyzed isomerizations of cubane. Synthesis and characterization of cuneane
Cubane, Cuneane, and Their Carboxylates:  A Calorimetric, Crystallographic, Calculational, and Conceptual Coinvestigation
Oxidation of 1-methylcyclobutene by metal ions
Unmasking Inherent Chirality within the Cubane Skeleton
Thermal Behaviour of C<sub>8</sub>H<sub>8</sub> Hydrocarbons Gas‐Phase Thermolysis of Cuneane, a New Example of a High‐Strain Energy Release Process
Programmable synthesis of multiply arylated cubanes through C–H metalation and arylation
Calculation of Optical Rotation Using Density Functional Theory
Cubane Chirality via Substitution of a “Hidden” Regular Tetrahedron
The Cubane System
Cubane: 50 Years Later
On the Discovery of Direct Ortho‐Magnesiation
Pseudotetrahedral Polyhalocubanes:  Synthesis, Structures, and Parity Violating Energy Differences
Data Provider (Database)
国立情報学研究所 : CiNii Research
Bibliographic ID (NDL)
12998992