Absolute stereochemistry of amphidinolide Q

Yohei Takahashi; Takaaki Kubota; Eri Fukushi; Jun Kawabata; Jun'ichi Kobayashi

doi:10.1021/ol8013123

Absolute stereochemistry of amphidinolide Q

Yohei Takahashi, Takaaki Kubota, Eri Fukushi, Jun Kawabata, Jun'ichi Kobayashi

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

15 Citations (Scopus)

Abstract

(Chemical Equation Presented) The absolute configurations at five chiral centers in amphidinolide Q (1), a cytotoxic 12-membered macrolide isolated from a marine dinoflagellate Amphidinium sp., were elucidated to be 4R, 7R, 9S, 11R, and 13R on the basis of NMR analyses and a modified Mosher's method,

Original language	English
Pages (from-to)	3709-3711
Number of pages	3
Journal	Organic Letters
Volume	10
Issue number	17
DOIs	https://doi.org/10.1021/ol8013123
Publication status	Published - 2008
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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

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10.1021/ol8013123

Cite this

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title = "Absolute stereochemistry of amphidinolide Q",

abstract = "(Chemical Equation Presented) The absolute configurations at five chiral centers in amphidinolide Q (1), a cytotoxic 12-membered macrolide isolated from a marine dinoflagellate Amphidinium sp., were elucidated to be 4R, 7R, 9S, 11R, and 13R on the basis of NMR analyses and a modified Mosher's method,",

author = "Yohei Takahashi and Takaaki Kubota and Eri Fukushi and Jun Kawabata and Jun'ichi Kobayashi",

year = "2008",

doi = "10.1021/ol8013123",

language = "English",

volume = "10",

pages = "3709--3711",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "17",

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TY - JOUR

T1 - Absolute stereochemistry of amphidinolide Q

AU - Takahashi, Yohei

AU - Kubota, Takaaki

AU - Fukushi, Eri

AU - Kawabata, Jun

AU - Kobayashi, Jun'ichi

PY - 2008

Y1 - 2008

N2 - (Chemical Equation Presented) The absolute configurations at five chiral centers in amphidinolide Q (1), a cytotoxic 12-membered macrolide isolated from a marine dinoflagellate Amphidinium sp., were elucidated to be 4R, 7R, 9S, 11R, and 13R on the basis of NMR analyses and a modified Mosher's method,

AB - (Chemical Equation Presented) The absolute configurations at five chiral centers in amphidinolide Q (1), a cytotoxic 12-membered macrolide isolated from a marine dinoflagellate Amphidinium sp., were elucidated to be 4R, 7R, 9S, 11R, and 13R on the basis of NMR analyses and a modified Mosher's method,

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U2 - 10.1021/ol8013123

DO - 10.1021/ol8013123

M3 - Article

C2 - 18680307

AN - SCOPUS:55949114723

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VL - 10

SP - 3709

EP - 3711

JO - Organic Letters

JF - Organic Letters

IS - 17

ER -

Absolute stereochemistry of amphidinolide Q

Abstract

ASJC Scopus subject areas

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