메뉴 건너뛰기




Volumn 132, Issue 29, 2010, Pages 10015-10017

Enantioselective organo-SOMO cascade cycloadditions: A rapid approach to molecular complexity from simple aldehydes and olefins

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC ALDEHYDE; CHEMICAL EFFICIENCY; COUPLING REACTION; CYCLIC PRODUCTS; CYCLOADDITIONS; ENAMINES; ENANTIOSELECTIVE; MOLECULAR COMPLEXITY; NUCLEOPHILIC ADDITIONS; OLEFIN ADDITION; RADICAL CATIONS;

EID: 77955826131     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja104313x     Document Type: Article
Times cited : (120)

References (19)
  • 1
    • 84962105974 scopus 로고
    • For reviews on the Diels-Alder reaction, see
    • Diels, O.; Alder, K. Justus Liebigs Ann. Chem. 1928, 460, 98. For reviews on the Diels-Alder reaction, see:
    • (1928) Justus Liebigs Ann. Chem. , vol.460 , pp. 98
    • Diels, O.1    Alder, K.2
  • 4
    • 77955822463 scopus 로고    scopus 로고
    • Cascade cycloaddition refers to a reaction that unites multiple reaction partners to form a cyclic product via a cascade mechanism, which is in accord with the IUPAC Gold Book definition of cycloaddition
    • Cascade cycloaddition refers to a reaction that unites multiple reaction partners to form a cyclic product via a cascade mechanism, which is in accord with the IUPAC Gold Book definition of cycloaddition.
  • 9
    • 70149104796 scopus 로고    scopus 로고
    • Correction
    • Correction: J. Am. Chem. Soc. 2009, 131, 6640.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 6640
  • 12
    • 0038800178 scopus 로고    scopus 로고
    • The radical-polar crossover reaction
    • Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Germany
    • Murphy, J. A. The Radical-Polar Crossover Reaction. In Radicals in Organic Synthesis; Renaud, P., Sibi, M. P., Eds.; Wiley-VCH: Weinheim, Germany, 2001; Vol. 1, p 298.
    • (2001) Radicals in Organic Synthesis , vol.1 , pp. 298
    • Murphy, J.A.1
  • 15
    • 77955781982 scopus 로고    scopus 로고
    • use of ceric ammonium nitrate as oxidant as in previous studies was, for this cascade cycloaddition, unsuccessful as it resulted in selective formation of benzylic nitrates see ref 7
    • The use of ceric ammonium nitrate as oxidant (as in previous studies) was, for this cascade cycloaddition, unsuccessful as it resulted in selective formation of benzylic nitrates (see ref 7).
  • 18
    • 65749085454 scopus 로고    scopus 로고
    • John Wiley & Sons, Inc.: Hoboken, NJ, 2009. For an illustrative example of counterion effects on carbocation stability
    • Olah, G. A.; Prakash, G. K. S.; Molnar, A.; Sommer, J. Superacid Chemistry; John Wiley & Sons, Inc.: Hoboken, NJ, 2009. For an illustrative example of counterion effects on carbocation stability
    • Superacid Chemistry
    • Olah, G.A.1    Prakash, G.K.S.2    Molnar, A.3    Sommer, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.