Stereochemical assignments for the two enantiomeric pairs of 9,10-dihydroxy-Δ6a(10a)-Tetrahydrocannabinols. X-Ray Crystal Structure Analysis of (±)-Trans-Cannabitriol
Publication
, Journal Article
McPhail, AT; ElSohly, HN; Turner, CE; ElSohly, MA
Published in: Journal of Natural Products
January 1, 1984
Single-crystal X-ray analysis of (±)-cannabitriol (1), isolated from Panamanian Cannabis, confirmed the structure of previously isolated (+)- and (-)-cannabitriol and defined the relative stereochemistry at the asymmetric centers. Based on the results obtained from this study, all compounds previously named cannabitriol [(+), (-), or (±)] should henceforth be designated trans-cannabitriol with appropriate sign of optical rotation, the other enantiomeric pair of (±)-9,10-dihydroxy-Δ6a(10a)-tetrahydrocannabinols being (±)-m-cannabitriol (4). © 1984, American Chemical Society. All rights reserved.
Duke Scholars
Published In
Journal of Natural Products
DOI
EISSN
1520-6025
ISSN
0163-3864
Publication Date
January 1, 1984
Volume
47
Issue
1
Start / End Page
138 / 142
Related Subject Headings
- Medicinal & Biomolecular Chemistry
- 4208 Traditional, complementary and integrative medicine
- 11 Medical and Health Sciences
- 06 Biological Sciences
- 03 Chemical Sciences
Citation
APA
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MLA
NLM
McPhail, A. T., ElSohly, H. N., Turner, C. E., & ElSohly, M. A. (1984). Stereochemical assignments for the two enantiomeric pairs of 9,10-dihydroxy-Δ6a(10a)-Tetrahydrocannabinols. X-Ray Crystal Structure Analysis of (±)-Trans-Cannabitriol. Journal of Natural Products, 47(1), 138–142. https://doi.org/10.1021/np50031a020
McPhail, A. T., H. N. ElSohly, C. E. Turner, and M. A. ElSohly. “Stereochemical assignments for the two enantiomeric pairs of 9,10-dihydroxy-Δ6a(10a)-Tetrahydrocannabinols. X-Ray Crystal Structure Analysis of (±)-Trans-Cannabitriol.” Journal of Natural Products 47, no. 1 (January 1, 1984): 138–42. https://doi.org/10.1021/np50031a020.
McPhail AT, ElSohly HN, Turner CE, ElSohly MA. Stereochemical assignments for the two enantiomeric pairs of 9,10-dihydroxy-Δ6a(10a)-Tetrahydrocannabinols. X-Ray Crystal Structure Analysis of (±)-Trans-Cannabitriol. Journal of Natural Products. 1984 Jan 1;47(1):138–42.
McPhail, A. T., et al. “Stereochemical assignments for the two enantiomeric pairs of 9,10-dihydroxy-Δ6a(10a)-Tetrahydrocannabinols. X-Ray Crystal Structure Analysis of (±)-Trans-Cannabitriol.” Journal of Natural Products, vol. 47, no. 1, Jan. 1984, pp. 138–42. Scopus, doi:10.1021/np50031a020.
McPhail AT, ElSohly HN, Turner CE, ElSohly MA. Stereochemical assignments for the two enantiomeric pairs of 9,10-dihydroxy-Δ6a(10a)-Tetrahydrocannabinols. X-Ray Crystal Structure Analysis of (±)-Trans-Cannabitriol. Journal of Natural Products. 1984 Jan 1;47(1):138–142.
Published In
Journal of Natural Products
DOI
EISSN
1520-6025
ISSN
0163-3864
Publication Date
January 1, 1984
Volume
47
Issue
1
Start / End Page
138 / 142
Related Subject Headings
- Medicinal & Biomolecular Chemistry
- 4208 Traditional, complementary and integrative medicine
- 11 Medical and Health Sciences
- 06 Biological Sciences
- 03 Chemical Sciences