TERPENOIDS: XIII. THE STEREOCHEMISTRY OF CHAPARRIN, CHAPARROL, AND RELATED COMPOUNDS-Reference-Cited by-同舟云学术

TERPENOIDS: XIII. THE STEREOCHEMISTRY OF CHAPARRIN, CHAPARROL, AND RELATED COMPOUNDS

Published:1965-11-01 Issue:11 Volume:43 Page:3008-3017
ISSN:0008-4042
Container-title:Canadian Journal of Chemistry
language:en
Short-container-title:Can. J. Chem.

Author:

Hollands T. R.,Mayo P. De,Nisbet M.,Crabbé P.

Abstract

Evidence is presented which leads to the absolute stereostructures XX, X, XI, and XII for chaparrin, chaparrol, isochaparrol, and neochaparrol respectively. The absolute configuration is arrived at by conversion to an optically active biphenyl (dihydrophenanthrene).

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Link

http://www.nrcresearchpress.com/doi/pdf/10.1139/v65-415

Reference13 articles.

1. Optical Rotatory Dispersion Studies. XC.1 The Octant Rule and the Isopropyl Group. Synthesis of Steroidal Isopropyl Ketones2

2. Optical rotatory dispersion studies—LXXXI stereochemical studies—XXVII

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enantioselective Synthesis of Atropisomers by Oxidative Aromatization with Central-to-Axial Conversion of Chirality;Molecules;2023-03-31

2. Bidirectional enantioselective synthesis of bis-benzofuran atropisomeric oligoarenes featuring two distal C–C stereogenic axes;Chemical Science;2020

3. Recent Applications of Optical Rotatory Dispersion and Optical Circular Dichroism in Organic Chemistry;Topics in Stereochemistry;2007-02-26

4. Formal Synthesis of Both Atropomers of Desertorin C and an Example of Chirality Transfer from a Biphenyl Axis to a Spiro Centre and its Reverse;Australian Journal of Chemistry;2000

5. Chirality transfer from a biphenyl axis to a spiro centre and its reverse: sequential self-immolation;Tetrahedron Letters;1999-04