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Journal ArticleDOI

Eight-membered ring templates for stereoselective radical cyclizations

Jeffrey D. Winkler, +2 more
- 01 Jan 1988 - 
- Vol. 29, Iss: 37, pp 4943-4946
TLDR
The ratio of cyclization to reduction of the cyclodec-6-enylmethyl radical depends critically on the alkene geometry as mentioned in this paper, which is a structural feature of the taxane diterpenes.
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This article is published in Tetrahedron Letters.The article was published on 1988-01-01. It has received 16 citations till now. The article focuses on the topics: Radical cyclization.

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Journal ArticleDOI

Programmierung organischer Moleküle: Design und Management organischer Synthesen über radikalische Kaskaden

TL;DR: In this paper, a discussion of the sagenhafte Spannweite of Kaskaden unimolekularer Radikalreaktionen is presented.
Reference EntryDOI

The McMurry Coupling and Related Reactions

TL;DR: McMurry coupling has been recognized as one of the most efficient methods for the synthesis of alkenes from carbonyl compounds as discussed by the authors, which can be applied to the preparation of various alkenets that are otherwise difficult to prepare.
Journal ArticleDOI

Synthesis of camphor based chiral crown ethers and their interactions with amino acid derivatives

TL;DR: In this paper, three camphor based crown ethers have been prepared, starting from (1R)-camphorquinone, in which 2-and 3-endo-substituents are used to regulate the availability of the endo-l8-crown-6 face for binding organic guests and the bridge head methyl group is available to impart enantioselectivity at the exo-face.
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