Conformational flexibility of longifolene

K. R. Acharya; S. S. Tavale; T. N.Guru Row

doi:10.1007/BF02840519

Conformational flexibility of longifolene

K. R. Acharya, S. S. Tavale, T. N.Guru Row

Department of Life Sciences

National Chemical Laboratory India

Research output: Contribution to journal › Article › peer-review

Abstract

The flexibility of the bicyclo[2.2.1]heptane-based tricyclic bridged system in longifolene is analysed based on x-ray structural data. In this context, the molecular structure of three differently substituted longifolenes has been analysed. The highly substituentdependent conformation provides scope for the synthesis of a variety of commercially oriented products.

Original language	English
Pages (from-to)	271-282
Number of pages	12
Journal	Proceedings of the Indian Academy of Sciences - Chemical Sciences
Volume	93
Issue number	3
DOIs	https://doi.org/10.1007/BF02840519
Publication status	Published - 1 Apr 1984

Keywords

cycloheptane conformation
longifolene derivatives
norbornane conformation
X-ray structure analysis

ASJC Scopus subject areas

General Chemistry

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10.1007/BF02840519

Cite this

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abstract = "The flexibility of the bicyclo[2.2.1]heptane-based tricyclic bridged system in longifolene is analysed based on x-ray structural data. In this context, the molecular structure of three differently substituted longifolenes has been analysed. The highly substituentdependent conformation provides scope for the synthesis of a variety of commercially oriented products.",

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AU - Tavale, S. S.

AU - Row, T. N.Guru

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Y1 - 1984/4/1

N2 - The flexibility of the bicyclo[2.2.1]heptane-based tricyclic bridged system in longifolene is analysed based on x-ray structural data. In this context, the molecular structure of three differently substituted longifolenes has been analysed. The highly substituentdependent conformation provides scope for the synthesis of a variety of commercially oriented products.

AB - The flexibility of the bicyclo[2.2.1]heptane-based tricyclic bridged system in longifolene is analysed based on x-ray structural data. In this context, the molecular structure of three differently substituted longifolenes has been analysed. The highly substituentdependent conformation provides scope for the synthesis of a variety of commercially oriented products.

KW - cycloheptane conformation

KW - longifolene derivatives

KW - norbornane conformation

KW - X-ray structure analysis

UR - https://www.scopus.com/pages/publications/51649169564

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DO - 10.1007/BF02840519

M3 - Article

AN - SCOPUS:51649169564

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VL - 93

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JO - Proceedings of the Indian Academy of Sciences - Chemical Sciences

JF - Proceedings of the Indian Academy of Sciences - Chemical Sciences

IS - 3

ER -

Conformational flexibility of longifolene

Abstract

Keywords

ASJC Scopus subject areas

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