Synthesis of Indolizine Derivatives and Their Reactions
نویسندگان
چکیده
منابع مشابه
One-pot Synthesis of Polysubstituted Indolizine Derivatives
An efficient approach to the synthesis of 1,2,3-trisubstituted indolizines is described via one-pot reactions of pyridine and dialkyl acetylendicarboxylate in the presence of ethyl 2-chloroacetoacetate in MeOH at room temperature. The corresponding 1, 2, 3-trisubstituted indolizines may be useful building blocks for the construction of complex indolizine derivatives.
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Stable derivatives of oxaphosphaphenanthrenes were prepared using multicomponent reactions of 3-bromo-2-naphthol, dialkyl acetylenedicarboxylate and trimethyl or triphenyl phosphite under microwave conditions with good yields.
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In order to verify if the triptycyl (the analog of triphenylmethyl in which the three phenyl groups were united to a CH) free radical 1a (Fig. 2.1) should be more instable than the triphenylmethyl radical itself, Bartlett et al. [1] first synthesized triptycene 1 in a low total yield by a multistep route starting from the Diels–Alder addition reaction of anthracene and benzoquinone (Scheme 2.1)...
متن کاملUltrasound-assisted 1,3-dipolar cycloaddition and cyclopropanation reactions for the synthesis of bis-indolizine and bis-cyclopropane derivatives.
Ultrasound irradiation can promote the 1,3-dipolar cycloaddition reaction of 2-chloropyridinium ylides with 2-benzylidenemalononitrile or 2,2'-(1,4-phenylenebis(methanylylidene))dimalononitrile, to afford the indolizine and bis-indolizine derivatives respectively. While the reaction of pyridinium ylides with 2-benzylidenemalononitrile or 2,2'-(1,4-phenylenebis(methanylylidene))dimalononitrile u...
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ژورنال
عنوان ژورنال: YAKUGAKU ZASSHI
سال: 1974
ISSN: 0031-6903,1347-5231
DOI: 10.1248/yakushi1947.94.7_839