Reductive cleavage of carboncarbon bond. A facile route to bridged eight membered rings related to taxanes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Synthetic studies on terpenoids. Part 19. Synthesis of 3β,10α,14β-trimethyl-1βH,11βH-tricyclo[9.3.0.0]tetradec-6-en-5-one, a tricyclic ketone related to the ophiobolins
2. Photochemical approach to the taxanes
3. Use of radical ring opening for introduction of alkyl and substituted alkyl groups with stereochemical control: a synthetic application of cyclopropylcarbinyl radicals
4. Free radical fragmentation of derivatives of [2 + 2] photoadducts
5. Cyano or acyl group migration by consecutive homolytic addition and β-fission
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1. Recent Advances in Transition-Metal-Catalyzed Functionalization of Unstrained Carbon–Carbon Bonds;Chemical Reviews;2014-07-25
2. Reductive Cleavage of the C sp 2C sp 3 Bond of Secondary Benzyl Alcohols: Rhodium Catalysis Directed by N-Containing Groups;Angewandte Chemie International Edition;2012-08-31
3. Reductive Cleavage of the C sp 2C sp 3 Bond of Secondary Benzyl Alcohols: Rhodium Catalysis Directed by N-Containing Groups;Angewandte Chemie;2012-08-31
4. ChemInform Abstract: Reductive Cleavage of Carbon-Carbon Bond. A Facile Route to Bridged Eight Membered Rings Related to Taxanes.;ChemInform;2010-08-21
5. Preparation of Alkenes;Compendium of Organic Synthetic Methods;2006-11-22
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