Macrocyclisation: The tin directed reaction of a carbohydrate derivative with succinyl chloride

Mathys M. Basson; Martin W. Bredenkamp; Cedric W. Holzapfel

doi:10.1016/S0040-4039(00)95263-8

Macrocyclisation: The tin directed reaction of a carbohydrate derivative with succinyl chloride

Mathys M. Basson, Martin W. Bredenkamp, Cedric W. Holzapfel

Chemical Sciences

University of Johannesburg

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

4 Citations (Scopus)

Abstract

Condensation of methyl 4,6-O-benzylidene-2,3-O-dibutylstanylene-α-D-glucopyranoside with succinyl chloride furnished two macrocyclic tetralactones, a hexalactone and an octalactone.

Original language	English
Pages (from-to)	591-594
Number of pages	4
Journal	Tetrahedron Letters
Volume	30
Issue number	5
DOIs	https://doi.org/10.1016/S0040-4039(00)95263-8
Publication status	Published - 1989

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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@article{fc7cda1a6875453d9260fd6b4a679a63,

title = "Macrocyclisation: The tin directed reaction of a carbohydrate derivative with succinyl chloride",

abstract = "Condensation of methyl 4,6-O-benzylidene-2,3-O-dibutylstanylene-α-D-glucopyranoside with succinyl chloride furnished two macrocyclic tetralactones, a hexalactone and an octalactone.",

author = "Basson, \{Mathys M.\} and Bredenkamp, \{Martin W.\} and Holzapfel, \{Cedric W.\}",

year = "1989",

doi = "10.1016/S0040-4039(00)95263-8",

language = "English",

volume = "30",

pages = "591--594",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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number = "5",

}

TY - JOUR

T1 - Macrocyclisation

T2 - The tin directed reaction of a carbohydrate derivative with succinyl chloride

AU - Basson, Mathys M.

AU - Bredenkamp, Martin W.

AU - Holzapfel, Cedric W.

PY - 1989

Y1 - 1989

N2 - Condensation of methyl 4,6-O-benzylidene-2,3-O-dibutylstanylene-α-D-glucopyranoside with succinyl chloride furnished two macrocyclic tetralactones, a hexalactone and an octalactone.

AB - Condensation of methyl 4,6-O-benzylidene-2,3-O-dibutylstanylene-α-D-glucopyranoside with succinyl chloride furnished two macrocyclic tetralactones, a hexalactone and an octalactone.

UR - https://www.scopus.com/pages/publications/45249130119

U2 - 10.1016/S0040-4039(00)95263-8

DO - 10.1016/S0040-4039(00)95263-8

M3 - Article

AN - SCOPUS:45249130119

SN - 0040-4039

VL - 30

SP - 591

EP - 594

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 5

ER -

Macrocyclisation: The tin directed reaction of a carbohydrate derivative with succinyl chloride

Abstract

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