Synthesis and Conformational Properties of Several Maximally Substituted Hexa(spirotetrahydrofuranyl)cyclohexanes. Assessment of the Pronounced Bias of the All-Trans D3d-Symmetric Isomer for Total Equatorial Oxygen Occupancy-Reference-Cited by-同舟云学术

Synthesis and Conformational Properties of Several Maximally Substituted Hexa(spirotetrahydrofuranyl)cyclohexanes. Assessment of the Pronounced Bias of the All-Trans D3d-Symmetric Isomer for Total Equatorial Oxygen Occupancy

Published:2000-12-01 Issue:26 Volume:65 Page:9172-9179
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Paquette Leo A.¹,Tae Jinsung¹,Branan Bruce M.¹,Bolin David G.¹,Eisenberg Shawn W. E.¹

Affiliation:

1. Evans Chemical Laboratories, The Ohio State University, Columbus, Ohio 43210

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0014313

Reference49 articles.

1. Definition of Several Control Elements Relevant to the Stereodefined Serial Elaboration of Belted Poly(spirotetrahydrofurans) Fitted with a Cyclohexane Core

2. Synthesis and Conformational Properties of the Sterically CrowdedD3d-Symmetric all-trans Hexa(spirotetrahydrofuranyl)cyclohexane System

3. Cyclic polyethers and their complexes with metal salts

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