An expeditious approach to tri-substituted chiral thiazolines

Raid J. Abdel-Jalil; Muhammad Saeed; Wolfgang Voelter

doi:10.1016/S0040-4039(01)00188-5

An expeditious approach to tri-substituted chiral thiazolines

Raid J. Abdel-Jalil, Muhammad Saeed, Wolfgang Voelter^*

^*المؤلف المقابل لهذا العمل

نتاج البحث: المساهمة في مجلة › Article › مراجعة النظراء

18 اقتباسات (Scopus)

ملخص

A regio- and stereoselective route from the cis-oriented epoxytriflate pentoses 1 and 4 via 4-amino-4-deoxy sugars 2 and 5 to chiral thiazoline derivatives 3a-e and 6a-e in high yields is described.

اللغة الأصلية	English
الصفحات (من إلى)	2435-2437
عدد الصفحات	3
دورية	Tetrahedron Letters
مستوى الصوت	42
رقم الإصدار	13
المعرِّفات الرقمية للأشياء	https://doi.org/10.1016/S0040-4039(01)00188-5
حالة النشر	Published - مارس 26 2001
منشور خارجيًا	نعم

ASJC Scopus subject areas

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الوصول إلى المستند

10.1016/S0040-4039(01)00188-5

الملفات والروابط الأخرى

قم بذكر هذا

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title = "An expeditious approach to tri-substituted chiral thiazolines",

abstract = "A regio- and stereoselective route from the cis-oriented epoxytriflate pentoses 1 and 4 via 4-amino-4-deoxy sugars 2 and 5 to chiral thiazoline derivatives 3a-e and 6a-e in high yields is described.",

author = "Abdel-Jalil, {Raid J.} and Muhammad Saeed and Wolfgang Voelter",

year = "2001",

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day = "26",

doi = "10.1016/S0040-4039(01)00188-5",

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journal = "Tetrahedron Letters",

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T1 - An expeditious approach to tri-substituted chiral thiazolines

AU - Abdel-Jalil, Raid J.

AU - Saeed, Muhammad

AU - Voelter, Wolfgang

PY - 2001/3/26

Y1 - 2001/3/26

N2 - A regio- and stereoselective route from the cis-oriented epoxytriflate pentoses 1 and 4 via 4-amino-4-deoxy sugars 2 and 5 to chiral thiazoline derivatives 3a-e and 6a-e in high yields is described.

AB - A regio- and stereoselective route from the cis-oriented epoxytriflate pentoses 1 and 4 via 4-amino-4-deoxy sugars 2 and 5 to chiral thiazoline derivatives 3a-e and 6a-e in high yields is described.

UR - http://www.scopus.com/inward/record.url?scp=0035952984&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0035952984&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(01)00188-5

DO - 10.1016/S0040-4039(01)00188-5

M3 - Article

AN - SCOPUS:0035952984

SN - 0040-4039

VL - 42

SP - 2435

EP - 2437

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 13

ER -

An expeditious approach to tri-substituted chiral thiazolines

ملخص

ASJC Scopus subject areas

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