Short and efficient chiral pool and RCM approach towards the synthesis of the macrocyclic core of the salicylihalamides

G. I. Georg; Mi Ahn Yu Mi Ahn; B. Blackman; F. Farokhi; P. T. Flaherty; C. J. Mossman; S. Roy; K. Yang

doi:10.1039/b008842k

Short and efficient chiral pool and RCM approach towards the synthesis of the macrocyclic core of the salicylihalamides

G. I. Georg
, Mi Ahn Yu Mi Ahn
, B. Blackman
, F. Farokhi
, P. T. Flaherty
, C. J. Mossman
, S. Roy
, K. Yang

Medicinal Chemistry

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

29 Scopus citations

Abstract

The macrolactone core structure of the salicylihalamides was prepared from diacetone-D-Glucose and via a ring-closing metathesis reaction.

Original language	English (US)
Pages (from-to)	255-256
Number of pages	2
Journal	Chemical Communications
Issue number	3
DOIs	https://doi.org/10.1039/b008842k
State	Published - Feb 7 2001

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@article{0c5838f605954324a3713a0c49bd033e,

title = "Short and efficient chiral pool and RCM approach towards the synthesis of the macrocyclic core of the salicylihalamides",

abstract = "The macrolactone core structure of the salicylihalamides was prepared from diacetone-D-Glucose and via a ring-closing metathesis reaction.",

author = "Georg, \{G. I.\} and \{Yu Mi Ahn\}, \{Mi Ahn\} and B. Blackman and F. Farokhi and Flaherty, \{P. T.\} and Mossman, \{C. J.\} and S. Roy and K. Yang",

year = "2001",

month = feb,

day = "7",

doi = "10.1039/b008842k",

language = "English (US)",

pages = "255--256",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "3",

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T1 - Short and efficient chiral pool and RCM approach towards the synthesis of the macrocyclic core of the salicylihalamides

AU - Georg, G. I.

AU - Yu Mi Ahn, Mi Ahn

AU - Blackman, B.

AU - Farokhi, F.

AU - Flaherty, P. T.

AU - Mossman, C. J.

AU - Roy, S.

AU - Yang, K.

PY - 2001/2/7

Y1 - 2001/2/7

N2 - The macrolactone core structure of the salicylihalamides was prepared from diacetone-D-Glucose and via a ring-closing metathesis reaction.

AB - The macrolactone core structure of the salicylihalamides was prepared from diacetone-D-Glucose and via a ring-closing metathesis reaction.

UR - https://www.scopus.com/pages/publications/0035819597

UR - https://www.scopus.com/pages/publications/0035819597#tab=citedBy

U2 - 10.1039/b008842k

DO - 10.1039/b008842k

M3 - Article

AN - SCOPUS:0035819597

SN - 1359-7345

SP - 255

EP - 256

JO - Chemical Communications

JF - Chemical Communications

IS - 3

ER -

Short and efficient chiral pool and RCM approach towards the synthesis of the macrocyclic core of the salicylihalamides

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