Advanced organic synthesis lect 2

advanced organic synthesis, methods and techniques - r. monson (1974) ww

advanced organic synthesis, methods and techniques - r. monson (1974) ww
... bp 8 6-8 7°, n£° 1.4729 endo-l-Acetoxy-8,8-dimethylbicyclo[2.2.2]oct-3-one-5,6-dicarboxylic acid gives the corresponding olefin, l-acetoxy-8,8-dimethylbicyclo[2.2.2]oct-2-ene-5-one, mp 5 9-6 0° after ... pentane (Chapter 8, Section IV) end0-l-Acetoxybicyclo[2.2.2]oct-3-one-5,6-dicarboxylic acid gives the corresponding olefin, l-acetoxybicyclo[2.2.2]oct-2-en-5-one, mp 4 9-5 0° after recrystallization from ... followed by methanol, and dried About 20 g of cis- and tran.s-4-ammocycloriexanecarboxylic acid, mp 29 2-2 96°, are obtained 3-Isoquinuclidone: A 5-g portion of cis- and tran.y-4-aminocyclohexanecarboxylic...
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Hóa hữu cơ nâng cao Tổng hợp phân tử phức tạp ( Advanced Organic Chemistry Synthesis of Complex Molecules )

Hóa hữu cơ nâng cao Tổng hợp phân tử phức tạp ( Advanced Organic Chemistry Synthesis of Complex Molecules )
... during the reaction: O • OH – Ru(VII) + 2e → Ru(V) TBSO 78% H3C CH3 HCH3O OTBS H H O O O O H O TBSO 2Ru(V) → Ru(VI) + Ru(IV) Julia-Lythgoe Olefination Ru(VI) + 2e– → Ru(IV) Griffith, W P.; Ley, S V.; ... Aldehyde (Ketone) R-CHO (RCOR ') hemiketal (hemiacetal) Oppenauer Oxidation Chromium (VI) Oxidants Sodium Hypochlorite N-Bromosuccinimide (NBS) Bromine Cerium (IV) Oxidants R Pyridinium Dichromate (PDC) ... Selectivity: (a) oxidation typically occurs at the more highly substituted terminus of the alkene (b) the order of reactivity of C–H bonds is CH2 > CH3 > CH [rule (a) takes precedence over rule (b)] (c)...
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Controlled Microwave Heating in Modern Organic Synthesis pot

Controlled Microwave Heating in Modern Organic Synthesis pot
... applications of controlled microwave heating in modern organic synthesis, and discusses some of the underlying phenomena and issues involved Introduction High-speed synthesis with microwaves has ... growing availability of microwave reactors in many laboratories, routine synthetic transformations are also now being carried out by microwave heating The benefits of controlled microwave heating, ... 15 minutes with microwave heating at 200 8C in NMP in open glass vessels A comparison of the kinetics of the thermal coupling of benzoic acid to the chlorinated Wang resin at 80 8C with the microwave- assisted...
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DNA-Templated Organic Synthesis: Natures Strategy for Controlling Chemical ReactivityApplied to Synthetic Molecules** doc

DNA-Templated Organic Synthesis: Natures Strategy for Controlling Chemical ReactivityApplied to Synthetic Molecules** doc
... challenges in using DTS to apply natures strategy for controlling chemical reactivity to molecules that can only be accessed through laboratory synthesis A reactant for DTS consists of three ... on several factors First, the absolute concentration of the reactants is critical For a DNA-templated reaction to proceed with a high ratio of templated to nontemplated product formation, reactants ... to serve as the starting material for a subsequent DNA-templated step, 3) the design of template architectures that increase the types of reactions which can be performed in a DNA-templated format,...
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bittner - organic synthesis workbook ii (wiley, 2001)

bittner - organic synthesis workbook ii (wiley, 2001)
... Copyright © 2001 Wiley-VCH Verlag GmbH ISBNs: 3-5 2 7-3 041 5-0 (Softcover); 3-5 2 7-6 001 3-2 (Electronic) Organic Synthesis Workbook II C Bittner, A S Busemann, U Griesbach, F Haunert, W.-R Krahnert, A Modi, ... Copyright © 2001 Wiley-VCH Verlag GmbH ISBNs: 3-5 2 7-3 041 5-0 (Softcover); 3-5 2 7-6 001 3-2 (Electronic) Organic Synthesis Workbook II C Bittner, A S Busemann, U Griesbach, F Haunert, W.-R Krahnert, A Modi, ... Copyright © 2001 Wiley-VCH Verlag GmbH ISBNs: 3-5 2 7-3 041 5-0 (Softcover); 3-5 2 7-6 001 3-2 (Electronic) Organic Synthesis Workbook II C Bittner, A S Busemann, U Griesbach, F Haunert, W.-R Krahnert, A Modi,...
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