✦ LIBER ✦

An expedient synthesis of 2-substituted naphthalenes from the Baylis–Hillman adducts

✍ Scribed by Jae Nyoung Kim; Yang Jin Im; Ji Hyeon Gong; Ka Young Lee

Publisher: Elsevier Science
Year: 2001
Tongue: French
Weight: 62 KB
Volume: 42
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)00687-6

No coin nor oath required. For personal study only.

✦ Synopsis

The reaction of 1, the acetates of the Baylis-Hillman adducts, and primary nitroalkanes 2 in the presence of potassium carbonate in N,N-dimethylformamide afforded 2-substituted naphthalenes 5 in good yields.

📜 SIMILAR VOLUMES

ChemInform Abstract: An Expedient Synthe

ChemInform Abstract: An Expedient Synthesis of 2-Substituted Naphthalenes from the Baylis—Hillman Adducts.

✍ Jae Nyoung Kim; Yang Jin Im; Ji Hyeon Gong; Ka Young Lee 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

ChemInform Abstract: An Expedient Synthe

ChemInform Abstract: An Expedient Synthesis of β-Phenyl-Substituted Baylis—Hillman and Aza-Baylis—Hillman Adducts

✍ Seong Jin Kim; Hyun Seung Lee; Jeong Mi Kim; Jae Nyoung Kim 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

ChemInform Abstract: Expedient Synthesis

ChemInform Abstract: Expedient Synthesis of 5-Benzoylpyrimidine-2,4-diones from Baylis—Hillman Adducts.

✍ Jeong Mi Kim; Eun Sun Kim; Jae Nyoung Kim 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 21 KB 👁 1 views

Regioselective synthesis of poly-substit

Regioselective synthesis of poly-substituted thiophenes from Baylis–Hillman adducts

✍ Hyun Seung Lee; Se Hee Kim; Jae Nyoung Kim 📂 Article 📅 2009 🏛 Elsevier Science 🌐 French ⚖ 242 KB

Antimalarial Activity of Baylis—Hillman

Antimalarial Activity of Baylis—Hillman Adducts from Substituted 2-Chloronicotinaldehydes.

✍ P. Narender; U. Srinivas; B. Gangadasu; Sukla Biswas; V. Jayathirtha Rao 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 17 KB 👁 2 views

The first successful intermolecular Heck

The first successful intermolecular Heck reaction of Baylis–Hillman adducts: synthesis of β-aryl substituted Baylis–Hillman adducts

✍ Jeong Mi Kim; Ko Hoon Kim; Taek Hyeon Kim; Jae Nyoung Kim 📂 Article 📅 2008 🏛 Elsevier Science 🌐 French ⚖ 122 KB

The first successful intermolecular Heck reaction between Baylis-Hillman adducts and aryl iodides was achieved under the conditions comprising Pd(OAc) 2 /n-Bu 4 NBr/KOAc in CH 3 CN.