Anhydro sugars to enantiomerically pure building blocks: Efficient syntheses of γ-lactones and furanoids

R. A. Al-Qawasmeh; T. H. Al-Tel; R. J. Abdel-Jalil; R. Thürmer; W. Voelter

Anhydro sugars to enantiomerically pure building blocks: Efficient syntheses of γ-lactones and furanoids

R. A. Al-Qawasmeh, T. H. Al-Tel, R. J. Abdel-Jalil, R. Thürmer, W. Voelter^*

^*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلة › Article › مراجعة النظراء

2 الاقتباسات (SciVal)

ملخص

Efficient and economic syntheses of multifunctional dihydrofurans, tetrahydrofurans and γ-lactones are described. The regiochemistry of the ring junctions of the annulated oxa ring systems are controlled using temporary or permanent protection of the C-4 hydroxyl group.

اللغة الأصلية	English
الصفحات (من إلى)	71-75
عدد الصفحات	5
دورية	Polish Journal of Chemistry
مستوى الصوت	73
رقم الإصدار	1
حالة النشر	Published - 1999
منشور خارجيًا	نعم

ASJC Scopus subject areas

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الملفات والروابط الأخرى

قم بذكر هذا

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title = "Anhydro sugars to enantiomerically pure building blocks: Efficient syntheses of γ-lactones and furanoids",

abstract = "Efficient and economic syntheses of multifunctional dihydrofurans, tetrahydrofurans and γ-lactones are described. The regiochemistry of the ring junctions of the annulated oxa ring systems are controlled using temporary or permanent protection of the C-4 hydroxyl group.",

keywords = "Anhydro sugars, Long-chain sugars, Optically pure tetrahydro- and dihydrofurans, Tricyclic furanoids, γ-lactones",

author = "Al-Qawasmeh, {R. A.} and Al-Tel, {T. H.} and Abdel-Jalil, {R. J.} and R. Th{\"u}rmer and W. Voelter",

year = "1999",

language = "English",

volume = "73",

pages = "71--75",

journal = "Polish Journal of Chemistry",

issn = "0137-5083",

publisher = "Polish Chemical Society",

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TY - JOUR

T1 - Anhydro sugars to enantiomerically pure building blocks

T2 - Efficient syntheses of γ-lactones and furanoids

AU - Al-Qawasmeh, R. A.

AU - Al-Tel, T. H.

AU - Abdel-Jalil, R. J.

AU - Thürmer, R.

AU - Voelter, W.

PY - 1999

Y1 - 1999

N2 - Efficient and economic syntheses of multifunctional dihydrofurans, tetrahydrofurans and γ-lactones are described. The regiochemistry of the ring junctions of the annulated oxa ring systems are controlled using temporary or permanent protection of the C-4 hydroxyl group.

AB - Efficient and economic syntheses of multifunctional dihydrofurans, tetrahydrofurans and γ-lactones are described. The regiochemistry of the ring junctions of the annulated oxa ring systems are controlled using temporary or permanent protection of the C-4 hydroxyl group.

KW - Anhydro sugars

KW - Long-chain sugars

KW - Optically pure tetrahydro- and dihydrofurans

KW - Tricyclic furanoids

KW - γ-lactones

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UR - http://www.scopus.com/inward/citedby.url?scp=0033474244&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0033474244

SN - 0137-5083

VL - 73

SP - 71

EP - 75

JO - Polish Journal of Chemistry

JF - Polish Journal of Chemistry

IS - 1

ER -

Anhydro sugars to enantiomerically pure building blocks: Efficient syntheses of γ-lactones and furanoids

ملخص

ASJC Scopus subject areas

الملفات والروابط الأخرى

بصمة

قم بذكر هذا