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Volumn , Issue 12, 2000, Pages 1815-1827

Oxygen to carbon rearrangements of anomerically linked alkenols from tetrahydropyran derivatives: An investigation of the reaction mechanism via a double isotopic labelling crossover study

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; ETHERS; HYDRIDES; OXYGEN; PROTONS; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 0034697707     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/a909300a     Document Type: Article
Times cited : (20)

References (26)
  • 25
    • 33645945403 scopus 로고    scopus 로고
    • The trans-homer is the predominant or only product seen in our previous work on oxygen to carbon rearrangements (see refs. 5-9).
    • The trans-homer is the predominant or only product seen in our previous work on oxygen to carbon rearrangements (see refs. 5-9).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.