Synthetic studies toward 13-Oxyingenol: Construction of the fully substituted tetracyclic compound

Takayuki Ohyoshi; Yamato Miyazawa; Kenta Aoki; Satomi Ohmura; Yuki Asuma; Ichiro Hayakawa; Hideo Kigoshi

doi:10.1021/ol103151k

Synthetic studies toward 13-Oxyingenol: Construction of the fully substituted tetracyclic compound

Takayuki Ohyoshi, Yamato Miyazawa, Kenta Aoki, Satomi Ohmura, Yuki Asuma, Ichiro Hayakawa, Hideo Kigoshi

Research output: Contribution to journal › Article › peer-review

14 Citations (Scopus)

Abstract

Chemical equations presented. 13-Oxyingenol and its derivatives have high levels of anti-HIV activity. A fully substituted tetracyclic skeleton of 13-oxyingenol is constructed by using spiro-cyclization and ring-closing olefin metathesis as key steps.

Original language	English
Pages (from-to)	2160-2163
Number of pages	4
Journal	Organic Letters
Volume	13
Issue number	9
DOIs	https://doi.org/10.1021/ol103151k
Publication status	Published - May 6 2011
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1021/ol103151k

Cite this

@article{0f2ef78043de4868bb212567e922f3c1,

title = "Synthetic studies toward 13-Oxyingenol: Construction of the fully substituted tetracyclic compound",

abstract = "Chemical equations presented. 13-Oxyingenol and its derivatives have high levels of anti-HIV activity. A fully substituted tetracyclic skeleton of 13-oxyingenol is constructed by using spiro-cyclization and ring-closing olefin metathesis as key steps.",

author = "Takayuki Ohyoshi and Yamato Miyazawa and Kenta Aoki and Satomi Ohmura and Yuki Asuma and Ichiro Hayakawa and Hideo Kigoshi",

year = "2011",

month = may,

day = "6",

doi = "10.1021/ol103151k",

language = "English",

volume = "13",

pages = "2160--2163",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "9",

}

TY - JOUR

T1 - Synthetic studies toward 13-Oxyingenol

T2 - Construction of the fully substituted tetracyclic compound

AU - Ohyoshi, Takayuki

AU - Miyazawa, Yamato

AU - Aoki, Kenta

AU - Ohmura, Satomi

AU - Asuma, Yuki

AU - Hayakawa, Ichiro

AU - Kigoshi, Hideo

PY - 2011/5/6

Y1 - 2011/5/6

N2 - Chemical equations presented. 13-Oxyingenol and its derivatives have high levels of anti-HIV activity. A fully substituted tetracyclic skeleton of 13-oxyingenol is constructed by using spiro-cyclization and ring-closing olefin metathesis as key steps.

AB - Chemical equations presented. 13-Oxyingenol and its derivatives have high levels of anti-HIV activity. A fully substituted tetracyclic skeleton of 13-oxyingenol is constructed by using spiro-cyclization and ring-closing olefin metathesis as key steps.

UR - http://www.scopus.com/inward/record.url?scp=79955587338&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=79955587338&partnerID=8YFLogxK

U2 - 10.1021/ol103151k

DO - 10.1021/ol103151k

M3 - Article

C2 - 21446676

AN - SCOPUS:79955587338

SN - 1523-7060

VL - 13

SP - 2160

EP - 2163

JO - Organic Letters

JF - Organic Letters

IS - 9

ER -

Synthetic studies toward 13-Oxyingenol: Construction of the fully substituted tetracyclic compound

Abstract

ASJC Scopus subject areas

UN SDGs

Access to Document

Other files and links

Fingerprint

Cite this