Acyclic Stereoselection in Natural Product Synthesis


NIH 1997 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1996 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1995 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1994 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1993 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1992 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1991 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1990 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1989 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley
NIH 1988 R37 AI	Acyclic Stereoselection in Natural Product Synthesis Heathcock, Clayton H. / University of California Berkeley

Heathcock, Clayton H; McLaughlin, Mark; Medina, Jesus et al. (2003) Multigram synthesis of the C29-C51 subunit and completion of the total synthesis of altohyrtin C (spongistatin 2). J Am Chem Soc 125:12844-9

Hubbs, Jed L; Heathcock, Clayton H (2003) A second-generation synthesis of the C1-C28 portion of the altohyrtins (spongistatins). J Am Chem Soc 125:12836-43

Wallace, G A; Scott, R W; Heathcock, C H (2000) Synthesis of the C29-C44 portion of spongistatin 1 (altohyrtin A). J Org Chem 65:4145-52

Scott, R W; Heathcock, C H (1996) An efficient synthesis of 3,4,6-tri-O-benzyl-2-C-methyl-D-glucal. Carbohydr Res 291:205-8

Montgomery, S H; Pirrung, M C; Heathcock, C H (1990) De novo synthesis of carbohydrates by stereoselective aldol reaction: L-cladinose. Carbohydr Res 202:13-32

Heathcock, C H; Finkelstein, B L; Aoki, T et al. (1985) Stereostructure of the archaebacterial C40 diol. Science 229:862-4