메뉴 건너뛰기




Volumn 73, Issue 15, 2008, Pages 5776-5785

Stereoselective synthesis of 3-oxygenated-ds-dialkyl-2,5-substituted tetrahydrofurans from cyclohexadienediols

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; OLEFINS; RAW MATERIALS; STEREOCHEMISTRY; STEREOSELECTIVITY;

EID: 48249133250     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800514k     Document Type: Article
Times cited : (16)

References (80)
  • 27
    • 33747291925 scopus 로고    scopus 로고
    • and references therein
    • Goksel, H.; Stark, C. B. W. Org. Lett. 2006, 8, 3433-3436, and references therein.
    • (2006) Org. Lett , vol.8 , pp. 3433-3436
    • Goksel, H.1    Stark, C.B.W.2
  • 40
    • 48249145254 scopus 로고    scopus 로고
    • 2/ Hexanes.
    • 2/ Hexanes.
  • 49
    • 48249136010 scopus 로고    scopus 로고
    • Huit, K
    • Patel, R. N, Ed, Marcel Dekker Inc, New York
    • (a) Berglund, Huit, K. In Stereoselective Biocatalysis; Patel, R. N., Ed.; Marcel Dekker Inc.: New York,
    • Stereoselective Biocatalysis
    • Berglund1
  • 52
    • 48249144297 scopus 로고    scopus 로고
    • To establish the usefulness of the methodology, in one run the deprotected diol was separated and recycled to give, after acetonization (95%), an additional 17% of 3a, which was thus obtained in a 57% overall yield.
    • To establish the usefulness of the methodology, in one run the deprotected diol was separated and recycled to give, after acetonization (95%), an additional 17% of 3a, which was thus obtained in a 57% overall yield.
  • 53
    • 48249134999 scopus 로고    scopus 로고
    • The change of the acetate for other acyl protecting group, namely, benzoate, was also performed. When the benzoate 10c (R = PhCO) was submitted to the cyclization conditions, clean deprotection of the acetonide was observed, giving the corresponding diol as the sole product in 85% yield.
    • The change of the acetate for other acyl protecting group, namely, benzoate, was also performed. When the benzoate 10c (R = PhCO) was submitted to the cyclization conditions, clean deprotection of the acetonide was observed, giving the corresponding diol as the sole product in 85% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.