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Volumn 75, Issue 19, 2010, Pages 6685-6688

Enantioselective and protecting group-free synthesis of 1-deoxythionojirimycin, 1-deoxythiomannojirimycin, and 1- deoxythiotalonojirimycin

Author keywords

[No Author keywords available]

Indexed keywords

BOROHYDRIDES; EFFICIENT SYNTHESIS; ENANTIOSELECTIVE; EXCHANGE RESIN; PROTECTING GROUP; SULFUR TRANSFER; TETRATHIOMOLYBDATE; TITLE COMPOUNDS;

EID: 77957160989     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1010125     Document Type: Article
Times cited : (20)

References (50)
  • 13
    • 34447326170 scopus 로고    scopus 로고
    • references cited therein
    • Mohan, S.; Pinto, B. M. Carbohydr. Res. 2007, 342, 1551 and references cited therein
    • (2007) Carbohydr. Res. , vol.342 , pp. 1551
    • Mohan, S.1    Pinto, B.M.2
  • 40
    • 77957152578 scopus 로고    scopus 로고
    • The low yield of products 8 and 11 is attributed to difficulties in isolation from the reaction medium.
    • The low yield of products 8 and 11 is attributed to difficulties in isolation from the reaction medium.
  • 41
    • 77957153751 scopus 로고    scopus 로고
    • 2S (DMSO, 30 min) gave a mixture of products from which bicyclic thialactone 12 could be isolated in 11% yield.
    • 2S (DMSO, 30 min) gave a mixture of products from which bicyclic thialactone 12 could be isolated in 11% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.