A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups

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Standard

A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups. / Yousefi, Naser-Abdul; Zimmermann, Morten L.; Bols, Mikael.

I: Beilstein Journal of Organic Chemistry, Bind 18, 17.11.2022, s. 1553-1559.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Yousefi, N-A, Zimmermann, ML & Bols, M 2022, 'A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups', Beilstein Journal of Organic Chemistry, bind 18, s. 1553-1559. https://doi.org/10.3762/bjoc.18.165

APA

Yousefi, N-A., Zimmermann, M. L., & Bols, M. (2022). A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups. Beilstein Journal of Organic Chemistry, 18, 1553-1559. https://doi.org/10.3762/bjoc.18.165

Vancouver

Yousefi N-A, Zimmermann ML, Bols M. A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups. Beilstein Journal of Organic Chemistry. 2022 nov. 17;18:1553-1559. https://doi.org/10.3762/bjoc.18.165

Author

Yousefi, Naser-Abdul ; Zimmermann, Morten L. ; Bols, Mikael. / A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups. I: Beilstein Journal of Organic Chemistry. 2022 ; Bind 18. s. 1553-1559.

Bibtex

@article{045a22ade58f4583bbe01eaad4e14401,
title = "A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups",
abstract = "An alpha-cyclodextrin protected with 2,4-dichlorobenzyl groups on the primary alcohols and ordinary benzyl groups on the secondary alcohols was prepared and subjected to DIBAL (diisobutylaluminum hydride)-promoted selective debenzylation. Debenzylation proceeded by first removing two dichlorobenzyl groups from the 6A,D positions and then removing one or two benzyl groups from the 3A,D positions.",
keywords = "aluminum hydrides, cyclodextrin, debenzylation, 2, 4-dichlorobenzyl, selective, POWERFUL, SUGARS",
author = "Naser-Abdul Yousefi and Zimmermann, {Morten L.} and Mikael Bols",
year = "2022",
month = nov,
day = "17",
doi = "10.3762/bjoc.18.165",
language = "English",
volume = "18",
pages = "1553--1559",
journal = "Beilstein Journal of Organic Chemistry",
issn = "2195-951X",
publisher = "Beilstein - Institut zur Foerderung der Chemischen Wissenschaften",

}

RIS

TY - JOUR

T1 - A study of the DIBAL-promoted selective debenzylation of alpha-cyclodextrin protected with two different benzyl groups

AU - Yousefi, Naser-Abdul

AU - Zimmermann, Morten L.

AU - Bols, Mikael

PY - 2022/11/17

Y1 - 2022/11/17

N2 - An alpha-cyclodextrin protected with 2,4-dichlorobenzyl groups on the primary alcohols and ordinary benzyl groups on the secondary alcohols was prepared and subjected to DIBAL (diisobutylaluminum hydride)-promoted selective debenzylation. Debenzylation proceeded by first removing two dichlorobenzyl groups from the 6A,D positions and then removing one or two benzyl groups from the 3A,D positions.

AB - An alpha-cyclodextrin protected with 2,4-dichlorobenzyl groups on the primary alcohols and ordinary benzyl groups on the secondary alcohols was prepared and subjected to DIBAL (diisobutylaluminum hydride)-promoted selective debenzylation. Debenzylation proceeded by first removing two dichlorobenzyl groups from the 6A,D positions and then removing one or two benzyl groups from the 3A,D positions.

KW - aluminum hydrides

KW - cyclodextrin

KW - debenzylation

KW - 2

KW - 4-dichlorobenzyl

KW - selective

KW - POWERFUL

KW - SUGARS

U2 - 10.3762/bjoc.18.165

DO - 10.3762/bjoc.18.165

M3 - Journal article

C2 - 36474968

VL - 18

SP - 1553

EP - 1559

JO - Beilstein Journal of Organic Chemistry

JF - Beilstein Journal of Organic Chemistry

SN - 2195-951X

ER -

ID: 327696977