Acylation of 5-phenyl-2-(fur-2-yl)oxazole

L. D. Patsenker; A. I. Lokshin; T. G. Drushlyak; V. N. Baumer

doi:10.1007/BF02320325

Acylation of 5-phenyl-2-(fur-2-yl)oxazole

L. D. Patsenker, A. I. Lokshin, T. G. Drushlyak, V. N. Baumer

نتاج البحث: نشر في مجلة › مقالة › مراجعة النظراء

ملخص

The ability of 5-phenyl-2-(fur-2-yl)oxazole to undergo acetylation and formylation is considered. It was established by x-ray structure analysis that electrophilic substitution proceeds at the position 5 of the furan ring. The direction of the reactions is analyzed from positions of the energy preference of transition states.

اللغة الأصلية	الإنجليزيّة
الصفحات (من إلى)	1266-1271
عدد الصفحات	6
دورية	Chemistry of Heterocyclic Compounds
مستوى الصوت	33
رقم الإصدار	11
المعرِّفات الرقمية للأشياء	https://doi.org/10.1007/BF02320325
حالة النشر	نُشِر - نوفمبر 1997
منشور خارجيًا	نعم

الوصول إلى المستند

10.1007/BF02320325

الملفات والروابط الأخرى

Link to publication in Scopus

قم بذكر هذا

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title = "Acylation of 5-phenyl-2-(fur-2-yl)oxazole",

abstract = "The ability of 5-phenyl-2-(fur-2-yl)oxazole to undergo acetylation and formylation is considered. It was established by x-ray structure analysis that electrophilic substitution proceeds at the position 5 of the furan ring. The direction of the reactions is analyzed from positions of the energy preference of transition states.",

author = "Patsenker, {L. D.} and Lokshin, {A. I.} and Drushlyak, {T. G.} and Baumer, {V. N.}",

year = "1997",

month = nov,

doi = "10.1007/BF02320325",

language = "אנגלית",

volume = "33",

pages = "1266--1271",

journal = "Chemistry of Heterocyclic Compounds",

issn = "0009-3122",

publisher = "Springer New York",

number = "11",

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TY - JOUR

T1 - Acylation of 5-phenyl-2-(fur-2-yl)oxazole

AU - Patsenker, L. D.

AU - Lokshin, A. I.

AU - Drushlyak, T. G.

AU - Baumer, V. N.

PY - 1997/11

Y1 - 1997/11

N2 - The ability of 5-phenyl-2-(fur-2-yl)oxazole to undergo acetylation and formylation is considered. It was established by x-ray structure analysis that electrophilic substitution proceeds at the position 5 of the furan ring. The direction of the reactions is analyzed from positions of the energy preference of transition states.

AB - The ability of 5-phenyl-2-(fur-2-yl)oxazole to undergo acetylation and formylation is considered. It was established by x-ray structure analysis that electrophilic substitution proceeds at the position 5 of the furan ring. The direction of the reactions is analyzed from positions of the energy preference of transition states.

UR - http://www.scopus.com/inward/record.url?scp=27544507014&partnerID=8YFLogxK

U2 - 10.1007/BF02320325

DO - 10.1007/BF02320325

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AN - SCOPUS:27544507014

SN - 0009-3122

VL - 33

SP - 1266

EP - 1271

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

IS - 11

ER -

Acylation of 5-phenyl-2-(fur-2-yl)oxazole

ملخص

الوصول إلى المستند

الملفات والروابط الأخرى

بصمة

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