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Volumn 13, Issue 5, 2011, Pages 1106-1109

A convergent synthesis of the C1-C16 segment of goniodomin A via palladium-catalyzed organostannane-thioester coupling

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN; ESTER; ETHER DERIVATIVE; GONIODOMIN A; MACROLIDE; ORGANOTIN COMPOUND; PALLADIUM;

EID: 79952119233     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1031409     Document Type: Article
Times cited : (32)

References (32)
  • 14
    • 79952132143 scopus 로고    scopus 로고
    • The carbon numbering corresponds to that of the natural product.
    • The carbon numbering corresponds to that of the natural product.
  • 31
    • 79952159026 scopus 로고    scopus 로고
    • 2, 0 °C, 3 h) uniformly gave an approximately 1:2:1 mixture of 2, 33, and 34, formation of these isomers during acid treatment of 32 could be ascribed to thermodynamic equilibration.
    • 2, 0 °C, 3 h) uniformly gave an approximately 1:2:1 mixture of 2, 33, and 34, formation of these isomers during acid treatment of 32 could be ascribed to thermodynamic equilibration.
  • 32
    • 79952175673 scopus 로고    scopus 로고
    • In the present study, we could only isolate natural (11 S)-spiroacetal 2 as a minor product. However, we expect that we would be able to control the C11 stereochemistry in a real system by constructing the macrocyclic framework of 1 prior to spiroacetalization.
    • In the present study, we could only isolate natural (11 S)-spiroacetal 2 as a minor product. However, we expect that we would be able to control the C11 stereochemistry in a real system by constructing the macrocyclic framework of 1 prior to spiroacetalization.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.