Titlebook: Advanced Organic Chemistry; Part B: Reactions an Francis A. Carey,Richard J. Sundberg Book 1983 Springer Science+Business Media New York 19

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書(shū)目名稱Advanced Organic Chemistry影響因子(影響力)




書(shū)目名稱Advanced Organic Chemistry影響因子(影響力)學(xué)科排名




書(shū)目名稱Advanced Organic Chemistry網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱Advanced Organic Chemistry網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱Advanced Organic Chemistry被引頻次




書(shū)目名稱Advanced Organic Chemistry被引頻次學(xué)科排名




書(shū)目名稱Advanced Organic Chemistry年度引用




書(shū)目名稱Advanced Organic Chemistry年度引用學(xué)科排名




書(shū)目名稱Advanced Organic Chemistry讀者反饋




書(shū)目名稱Advanced Organic Chemistry讀者反饋學(xué)科排名

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Gef?hrdung von Küsten-und Meeres?kosystemenllow two molecular fragments to be connected by the reaction of a nucleophilic carbon with an electrophilic one can be crucial to the success of a synthetic plan. The emphasis in this chapter is on . and ., two of the most useful kinds of carbon nucleophiles, their preparation, and their reactions w

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Küsten- und Meeres?kosysteme in Europa., .. All of these processes involve, at some point, the addition of a carbon nucleophile to a carbonyl group. The type of product which is isolated depends on the nature of the substituent (X) on the carbon nucleophile, the substituents (A and B) on the carbonyl group, and the ways in which A, B, a

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Zum Gegenstand des rechtlichen Schwerpunktesn Chapter 1 involve attack by carbon nucleophiles at . . centers, while those discussed in Chapter 2 involved reaction at . . centers, primarily carbonyl groups. In this chapter we turn our attention to noncarbon nucleophiles. Nucleophilic substitution both at . . and . . centers is used in a variet

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