(+)-Cannabispirenone-a: Synthesis and absolute configuration

N. R. Natale; Brian E. Marron; Eric J. Evain; Craig D. Dodson

doi:10.1080/00397918408063744

(+)-Cannabispirenone-a: Synthesis and absolute configuration

N. R. Natale
, Brian E. Marron
, Eric J. Evain
, Craig D. Dodson

University of Idaho

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

10 Scopus citations

Abstract

An efficient asymmetric synthesis of cannabispirenone-A (la) has been accomplished. The absolute configuration of the (+)-(la) is assigned as R. The magnitude of rotation calls the optical purity of the natural product into question.

Original language	English
Pages (from-to)	599-603
Number of pages	5
Journal	Synthetic Communications
Volume	14
Issue number	7
DOIs	https://doi.org/10.1080/00397918408063744
State	Published - Jun 1 1984

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10.1080/00397918408063744

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title = "(+)-Cannabispirenone-a: Synthesis and absolute configuration",

abstract = "An efficient asymmetric synthesis of cannabispirenone-A (la) has been accomplished. The absolute configuration of the (+)-(la) is assigned as R. The magnitude of rotation calls the optical purity of the natural product into question.",

author = "Natale, \{N. R.\} and Marron, \{Brian E.\} and Evain, \{Eric J.\} and Dodson, \{Craig D.\}",

year = "1984",

month = jun,

day = "1",

doi = "10.1080/00397918408063744",

language = "English",

volume = "14",

pages = "599--603",

journal = "Synthetic Communications",

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TY - JOUR

T1 - (+)-Cannabispirenone-a

T2 - Synthesis and absolute configuration

AU - Natale, N. R.

AU - Marron, Brian E.

AU - Evain, Eric J.

AU - Dodson, Craig D.

PY - 1984/6/1

Y1 - 1984/6/1

N2 - An efficient asymmetric synthesis of cannabispirenone-A (la) has been accomplished. The absolute configuration of the (+)-(la) is assigned as R. The magnitude of rotation calls the optical purity of the natural product into question.

AB - An efficient asymmetric synthesis of cannabispirenone-A (la) has been accomplished. The absolute configuration of the (+)-(la) is assigned as R. The magnitude of rotation calls the optical purity of the natural product into question.

UR - https://www.scopus.com/pages/publications/0008822936

U2 - 10.1080/00397918408063744

DO - 10.1080/00397918408063744

M3 - Article

AN - SCOPUS:0008822936

SN - 0039-7911

VL - 14

SP - 599

EP - 603

JO - Synthetic Communications

JF - Synthetic Communications

IS - 7

ER -

(+)-Cannabispirenone-a: Synthesis and absolute configuration

Abstract

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