Design and synthesis of Spirocyclics via the Diels alder reaction and ring-opening cross-metathesis as key steps

Kotha, Sambasivarao ; Ashoke, Deb C. ; Subrata, Chattopadhyay (2006) Design and synthesis of Spirocyclics via the Diels alder reaction and ring-opening cross-metathesis as key steps Letters in Organic Chemistry, 3 (2). pp. 128-134. ISSN 1570-1786

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Abstract

Ring-opening-cross-metathesis (ROCM) reaction has been used to prepare spiro-indane derivatives containing six rings. The Diels-Alder (DA) chemistry of indan-2-spiro(cyclopenta-2,4-diene) 1 with various dienophiles such as 1,4-benzoquinone and its derivatives gave the corresponding DA products in moderate to good yields. Also, we report an improved procedure for preparation of the spiro-diene 1 using phase-transfer catalysis (PTC) conditions.

Item Type:Article
Source:Copyright of this article belongs to Bentham Science Publishers.
Keywords:Spirocycles; ROCM; Diels-Alder; Grubbs' Catalyst; Quinones; Spiro-diene; Fenestranes
ID Code:82037
Deposited On:09 Feb 2012 04:26
Last Modified:09 Feb 2012 04:27

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