Conformational behavior of 3-borabicyclo[3.3.1]nonanes-Reference-Cited by-同舟云学术

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Conformational behavior of 3-borabicyclo[3.3.1]nonanes

Published:1999-11 Issue:2 Volume:590 Page:227-233
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Gurskii Mikhail E,Gridnev Ilya D,Bubnov Yuri N,Pelter Andrew,Rademacher Paul

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference20 articles.

1. 3,7-disubstituted bicyclo[3.3.1]nonanes—III

2. 13C NMR spectroscopy of some 3- and 7-substituted bicyclo[3.3.1]nonanes

3. Chair-boat equilibria in bicyclo[3.3.1]nonane and some 3- and 3,7-substituted derivatives

4. 13C-NMR-Spektroskopische und stereochemische untersuchungen—XIV

5. Y. Senda, J.I. Ishiyama, S. Imaizumi, J. Chem. Soc. Perkin Trans. 2 (1981) 90.

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1. Different routes for the construction of biologically active diversely functionalized bicyclo[3.3.1]nonanes: an exploration of new perspectives for anticancer chemotherapeutics;RSC Advances;2023

2. Sigmatropic [1,3]-boron shift (permanent allylic rearrangement) in 3-allyl-3-borabicyclo[3.3.1]nonanes;Russian Chemical Bulletin;2014-02

3. Nuclear magnetic resonance data of C17H25BO;Chemical Shifts and Coupling Constants for Boron-11;2009

4. Allylboranes and the synthesis of diamond molecules;Russian Chemical Bulletin;2008-04

5. Unique stereochemistry of 3-borabicyclo[3.3.1]nonane derivatives;Russian Chemical Bulletin;2004-09

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