ホルボール (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ホルボール" in Japanese language version.

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1stanford.edu

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pubs.acs.org

Wender, P. A.; Kogen, H.; Lee, H.-Y.; Munger, J. D., Jr.; Wilhelm, R. S.; Williams, P. D. (1989). “Studies on tumor promoters. 8. The synthesis of phorbol”. J. Am. Chem. Soc. 111: 8957. doi:10.1021/ja00206a050.

doi.org

Flaschenträger B, v. Wolffersdorff R (1934). “Über den Giftstoff des Crotonöles. 1. Die Säuren des Crotonöles”. Helvetica Chimica Acta 17 (1): 1444–1452. doi:10.1002/hlca.193401701179.
Flaschenträger B, Wigner G (1942). “Über den Giftstoff des Crotonöles. V. Die Gewinnung von Crotonharz, Dünnem Öl und Phorbol aus dem Crotonöl durch Alkoholyse”. Helvetica Chimica Acta 25 (3): 569–581. doi:10.1002/hlca.19420250315.
Kauffmann T, Neumann H, Lenhardt K (1959). “Zur Konstitution des Phorbols, I. Über die reduzierende Gruppe des Phorbols”. Chemische Berichte 92 (8): 1715–1726. doi:10.1002/cber.19590920802.
Kauffmann T, Eisinger A, Jasching W, Lenhardt K (1959). “Zur Konstitution des Phorbols, I. Über die reduzierende Gruppe des Phorbols”. Chemische Berichte 92 (8): 1727–1738. doi:10.1002/cber.19590920803.
Tseng S-S, Van Duuren BL, Solomon JJ (1977). “Synthesis of 4aα-phorbol 9-myristate 9a-acetate and related esters”. J. Org. Chem. 42 (33): 3645–3649. doi:10.1021/jo00443a002.
Hecker E, Bartsch H, Bresch H, Gschwendt M, Härle B, Kreibich G, Kubinyi H, Schairer HU, Szczepanski Ch v, Thielmann HW (1967). “Structure and stereochemistry of the tetracyclic diterpene phorbol from croton tiglium L”. Tetrahedron Lett. 8 (33): 3165–3170. doi:10.1016/S0040-4039(01)89890-7.
Pettersen RC, Ferguson G, Crombie L, Games ML, Pointer DJ (1967). “The structure and stereochemistry of phorbol, diterpene parent of co-carcinogens of croton oil”. Chem. Commun. (London): 716. doi:10.1039/C19670000716.
Paul A. Wender, Jung-Min Kee, Jeffrey M. Warrington (May 2008). “Practical Synthesis of Prostratin, DPP, and Their Analogs, Adjuvant Leads Against Latent HIV”. Science 320 (5876): 649–652. doi:10.1126/science.1154690. PMC 2704988. PMID 18451298.
Wender, P. A.; Kogen, H.; Lee, H.-Y.; Munger, J. D., Jr.; Wilhelm, R. S.; Williams, P. D. (1989). “Studies on tumor promoters. 8. The synthesis of phorbol”. J. Am. Chem. Soc. 111: 8957. doi:10.1021/ja00206a050.
Kawamura, Shuhei; Chu, Hang; Felding, Jakob; Baran, Phil S. (2016). “Nineteen-step total synthesis of (+)-phorbol”. Nature 532 (7597): 90–3. Bibcode: 2016Natur.532...90K. doi:10.1038/nature17153. PMC 4833603. PMID 27007853. .

harvard.edu

ui.adsabs.harvard.edu

Kawamura, Shuhei; Chu, Hang; Felding, Jakob; Baran, Phil S. (2016). “Nineteen-step total synthesis of (+)-phorbol”. Nature 532 (7597): 90–3. Bibcode: 2016Natur.532...90K. doi:10.1038/nature17153. PMC 4833603. PMID 27007853. .

nih.gov

stanford.edu

news.stanford.edu

Louis Bergeron, Stanford University (2008年5月1日). “Researchers synthesize plant compound to flush out HIV”. Stanford Press. 2010年10月28日閲覧。