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Volumn 65, Issue 21, 2009, Pages 4182-4189

A flexible route to new spirodioxanes, oxathianes, and morpholines

Author keywords

[No Author keywords available]

Indexed keywords

1 [[(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHOXY] 3 [[(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL]THIO]PROPANONE O BENZYLOXIME; 1 [[(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL]AMINO] 3 [(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHOXY]PROPANONE O BENZYLOXIME; 1 [[(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL]AMINO] 3 [[(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL]THIO]PROPANONE O BENZYLOXIME; 1 CHLORO 3 [(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHOXY]PROPANONE O BENZYLOXIME; 1 CHLORO 3 [[(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL]THIO]PROPANONE O BENZYLOXIME; 2,8 DIHYDROXYMETHYL 10 BENZOYL 10 AZA 1,4,7 TRIOXASPIRO[5.5]UNDECANE; 2,8 DIHYDROXYMETHYL 4 THIA 1,7,10 TRIOXASPIRO [5.5]UNDECANE; MORPHOLINE DERIVATIVE; N [(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL] N 3 [(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHOXY] 2 [[(BENZYLOXY)IMINO]PROPYL]BENZAMIDE; N [(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL] N [3 [(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL]THIO] 2 [[(BENZYLOXY)IMINO]PROPYL]BENZAMIDE; NATURAL PRODUCT; NUCLEOPHILE; OXANTHIANE DERIVATIVE; OXIME DERIVATIVE; SOLKETAL DERIVATIVE; SPIRODIOXANE DERIVATIVE; SPIROKETAL DERIVATIVE; TERTBUTYL [2,3 DIHYDROXYPROPYL]3 [(2,3-DIHYDROXYPROPYL)THIO] [2 [(BENZYLOXY)IMINO]PROPYL]CARBAMATE; TERTBUTYL [[(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL][3 [(2,2 DIMETHYL 1,3 DIOXOLAN 4 YL)METHYL]THIO] [2 [(BENZYLOXY)IMINO]PROPYL]CARBAMATE; UNCLASSIFIED DRUG;

EID: 64649098901     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.03.044     Document Type: Article
Times cited : (4)

References (39)
  • 5
    • 64649094857 scopus 로고    scopus 로고
    • For recent reviews on spiroketal syntheses see
    • For recent reviews on spiroketal syntheses see:
  • 20
    • 64649104195 scopus 로고    scopus 로고
    • For synthesis based on a methylene strategy see
    • For synthesis based on a methylene strategy see:
  • 24
    • 64649106317 scopus 로고    scopus 로고
    • For synthesis based on a hydrazone strategy, see
    • For synthesis based on a hydrazone strategy, see:
  • 28
    • 64649089711 scopus 로고    scopus 로고
    • For an account of natural product synthesis based on a dithiane strategy see
    • For an account of natural product synthesis based on a dithiane strategy see:
  • 29
  • 37
    • 0033583281 scopus 로고    scopus 로고
    • The methylene group in the α position of the benzyloxime function is shielded when placed in a cis position relative to the benzyloxy group see:
    • The methylene group in the α position of the benzyloxime function is shielded when placed in a cis position relative to the benzyloxy group see:. Naito T., Nakagawa K., Nakamura T., Kasei A., Ninomiya I., and Kiguchi T. J. Org. Chem. 64 (1999) 2003-2009
    • (1999) J. Org. Chem. , vol.64 , pp. 2003-2009
    • Naito, T.1    Nakagawa, K.2    Nakamura, T.3    Kasei, A.4    Ninomiya, I.5    Kiguchi, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.