A unified approach to trans -hydrindane sesterterpenoids

Daniel T. Hog; Peter Mayer; Dirk Trauner

doi:10.1021/jo300726z

A unified approach to trans -hydrindane sesterterpenoids

Daniel T. Hog, Peter Mayer, Dirk Trauner

Chemistry

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

Abstract

A synthetic approach to several sesterterpenoids containing an isopropyl trans-hydrindane system is presented. Its most remarkable feature is the stereochemical diversification of a common precursor through the choice of different hydrogenation conditions.

Original language	English (US)
Pages (from-to)	5838-5843
Number of pages	6
Journal	Journal of Organic Chemistry
Volume	77
Issue number	13
DOIs	https://doi.org/10.1021/jo300726z
State	Published - Jul 6 2012

ASJC Scopus subject areas

Organic Chemistry

Access to Document

10.1021/jo300726z

Cite this

@article{902e969eb0bc429a8f75f945792ecf44,

title = "A unified approach to trans -hydrindane sesterterpenoids",

abstract = "A synthetic approach to several sesterterpenoids containing an isopropyl trans-hydrindane system is presented. Its most remarkable feature is the stereochemical diversification of a common precursor through the choice of different hydrogenation conditions.",

author = "Hog, {Daniel T.} and Peter Mayer and Dirk Trauner",

year = "2012",

month = jul,

day = "6",

doi = "10.1021/jo300726z",

language = "English (US)",

volume = "77",

pages = "5838--5843",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "13",

}

TY - JOUR

T1 - A unified approach to trans -hydrindane sesterterpenoids

AU - Hog, Daniel T.

AU - Mayer, Peter

AU - Trauner, Dirk

PY - 2012/7/6

Y1 - 2012/7/6

N2 - A synthetic approach to several sesterterpenoids containing an isopropyl trans-hydrindane system is presented. Its most remarkable feature is the stereochemical diversification of a common precursor through the choice of different hydrogenation conditions.

AB - A synthetic approach to several sesterterpenoids containing an isopropyl trans-hydrindane system is presented. Its most remarkable feature is the stereochemical diversification of a common precursor through the choice of different hydrogenation conditions.

UR - http://www.scopus.com/inward/record.url?scp=84863620825&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84863620825&partnerID=8YFLogxK

U2 - 10.1021/jo300726z

DO - 10.1021/jo300726z

M3 - Article

C2 - 22651375

AN - SCOPUS:84863620825

SN - 0022-3263

VL - 77

SP - 5838

EP - 5843

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 13

ER -

A unified approach to trans -hydrindane sesterterpenoids

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this