Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

POTENTIAL ANTIRADIATION DRUGS. II. /cap beta/-AMINOMERCAPTANS DERIVED FROM D-ALLOSE

Journal Article · · Journal of the American Chemical Society (U.S.)
DOI:https://doi.org/10.1021/ja01479a022· OSTI ID:4838856
A complex neighboring group approach provided a suc cessful synthesis of methyl 3-amino-2,3-dideoxy-2mercapto- alpha -D-allopyranoside hydrochloride(IX). The blocked 3-aminoaltroside(II) afforded, in two steps, the crystalline dithiocarbamovl mesylate(VI) which, heated in pyridine, cyclized to the thiazoline V, that was reduced to the thiazolidine IV. Compound IV was deblocked and hydrolyzed, via the crystalline mercuric salt VIII, to the aminomercapto glycoside IX. (auth)
Research Organization:
Stanford Research Inst., Menlo Park, Calif.
Sponsoring Organization:
USDOE
NSA Number:
NSA-15-032059
OSTI ID:
4838856
Journal Information:
Journal of the American Chemical Society (U.S.), Journal Name: Journal of the American Chemical Society (U.S.) Vol. Vol: 83; ISSN JACSA
Country of Publication:
Country unknown/Code not available
Language:
English

Similar Records

POTENTIAL ANTIRADIATION DRUGS. III. /cap beta/-AMINOMERCAPTANS DERIVED FROM D-ALTROSE
Journal Article · Wed Sep 20 00:00:00 EDT 1961 · Journal of the American Chemical Society (U.S.) · OSTI ID:4825477

SYNTHESIS OF POTENTIAL ANTIRADIATION DRUGS. Annual Summary Report, October 1, 1961-September 30, 1962. Report No. 39
Technical Report · Wed Oct 31 23:00:00 EST 1962 · OSTI ID:4656787

Antiradiation agents. 3-[(alkylthio)alkyl]thiazolidines and substituted 2- ([(3-thiazolidinyl)alkyl]thio)pyridines and -quinolines
Journal Article · Sat Mar 31 23:00:00 EST 1973 · J. Med. Chem., v. 16, no. 4, pp. 328-331 · OSTI ID:4413636