Studies related to the total synthesis of pentostatin: An efficient, regiospecific glycosylation of 6,7-dihydroimidazo[4,5-d][1,2]diazepin-8(3H)-one and related homologs.-Reference-Cited by-同舟云学术

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Studies related to the total synthesis of pentostatin: An efficient, regiospecific glycosylation of 6,7-dihydroimidazo[4,5-d][1,2]diazepin-8(3H)-one and related homologs.

Published:1981-01 Issue:33 Volume:22 Page:3155-3158
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Showalter H.D.Hollis,Putt Sterling R

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference6 articles.

1. ISOLATION AND PROPERTIES OF A VIDARABINE DEAMINASE INHIBITOR, CO-VIDARABINE

2. A total synthesis of pentostatin, the potent inhibitor of adenosine deaminase

3. Structure of coformycin, an unusual nucleoside of microbial origin

4. A General Synthesis of Pyrimidine Nucleosides

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1. An Expedient Route to Imidazo[1,4]diazepin-7-ones via A Post-Ugi Gold-Catalyzed Heteroannulation;Organic Letters;2013-04-01

2. Synthesis and electrochemical evaluation of substituted imidazo[4,5-d]pyrrolo[3,2-f][1,3] diazepine scaffolds;Tetrahedron;2012-06

3. (8S)-3-(2-Deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl)-3,6,7,8-tetrahydroimidazo[4,5-d][1,3]diazepin-8-ol;Acta Crystallographica Section E Structure Reports Online;2006-09-06

4. Tin(IV) Chloride;Encyclopedia of Reagents for Organic Synthesis;2005-10-15

5. Tin(IV) Chloride;Encyclopedia of Reagents for Organic Synthesis;2005-10-15

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